Terpenoids and Glycosides
The terpenoids are a large and diverse class of naturally occurring organic chemicals, derived from five-carbon isoprene unitsassembled and modified in thousands of ways. Most are multicyclic structures that differ from one another not only in functionalgroups but also in their basic carbon skeletons. They can be classified according to the number of isoprene units used:Hemiterpenoids, Monoterpenoids, Sesquiterpenoids, Diterpenoids, Sesterterpenoids, Triterpenoids, Tetraterpenoids. These lipidscan be found in all classes of living things, and are the largest group of natural products. Plant terpenoids are used extensively fortheir aromatic qualities and play a role in traditional herbal remedies. Terpenoids contribute to the scent of eucalyptus, the flavorsof cinnamon, cloves, and ginger, the yellow color in sunflowers, and the red color in tomatoes.
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Terpenoids and Glycosides Inhibitors & Modulators
(+)-Borneol (d-Borneol) Cat. No.: HY-N1368A
(+)-Borneol (d-Borneol) is a natural bicyclicmonoterpene used for analgesia and anesthesia intraditional Chinese medicine; enhances GABA
activity with an of 248 μM.receptor EC50
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
(+)-Camphor (D-(+)-Camphor; (1R)-(+)-Camphor) Cat. No.: HY-B1173
(+)-Camphor is an ingredient in cooking, and as anembalming fluid for medicinal purposes,.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 500 mg
(+)-Dehydroabietic acidCat. No.: HY-N2546
(+)-Dehydroabietic acid is a diterpenoid.(+)-Dehydroabietic acid can be used for theacrylamide Hydrogel synthesis.
Purity: >98%Clinical Data: No Development ReportedSize: 10 mg, 25 mg, 50 mg, 100 mg
(+)-LongifoleneCat. No.: HY-N6662
(+)-Longifolene is a sesquiterpenoid and ametabolite in rabbits. (+)-Longifolen is convertedto primary, secondary or tertiary alcohols inrabbits, among which the primary alcohol ispredominant.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
(+)-trans-IsolimoneneCat. No.: HY-N7250
(+)-trans-Isolimonene is a natural monoterpeneisolated from essential oil.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
(-)-AltenueneCat. No.: HY-N6713
(-)-Altenuene is a heptaketide isolated from anendolichenic fungal strain .Nigrospora sphaerica
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg
(-)-Borneol (L-Borneol) Cat. No.: HY-N1368B
(-)-Borneol has a highly efficacious positivemodulating action at receptor with an GABA EC50
of 237 μM.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
(-)-Cedrene (α-cedrene) Cat. No.: HY-135190
(-)-Cedrene (α-cedrene) is a sesquiterpeneconstituent of cedarwood oils, with anti-leukemic,antimicrobial and anti-obesity activities.
Purity: >98.0%Clinical Data: No Development ReportedSize: 1 mL, 5 mL
(-)-FenchoneCat. No.: HY-N5132
(-)-Fenchone, a bicyclic monoterpene, is widelydistributed in plants and found in essential oilsfrom .Thuja occidentalis
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 500 mg
(-)-Limonene ((S)-(-)-Limonene) Cat. No.: HY-Z0478
(-)-Limonene ((S)-(-)-Limonene) is a monoterpenefound in many pine-needle oils and in turpentine.(-)-Limonene can induce a mild bronchoconstrictiveeffect.
Purity: >95.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
2 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
(-)-MentholCat. No.: HY-75161
(-)-Menthol is a key component of peppermint oilthat binds and activates transient receptorpotential melastatin 8 ( ), aTRPM8Ca -permeable nonselective cation channel, to2+
increase [Ca ] . Antitumor activity.2+i
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 500 mg, 1 g
(-)-α-PineneCat. No.: HY-N0549
(-)-α-Pinene is a monoterpene and shows sleepenhancing property through a direct binding toGABAA-benzodiazepine (BZD) receptors by acting asa partial modulator at the BZD binding site.
Purity: 99.63%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg, 1 g, 5 g
(-)-α-Terpineol ((S)-α-Terpineol) Cat. No.: HY-N1467
(-)-α-Terpineol ((S)-α-Terpineol), a monoterpenecompound, is one of important aroma compounds inwhite wines.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
(20R)-Ginsenoside Rh1Cat. No.: HY-N1400
(20R)-Ginsenoside Rh1, the R isomer of GinsenosideRh1 isolated from , inhibits thePanax Ginsengthrombin-induced conversion of fibrinogen tofibrin.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
(20R)-ProtopanaxadiolCat. No.: HY-N2040
(20R)-Protopanaxadiol is a triterpenoid saponinmetabolite of 20(R)-ginsenoside Rg3 in blackginseng. (20R)-Protopanaxadiol exhibits anti-tumoractivity and cytotoxicity, and potently inhibitsthe growth of .Helicobacter pylori
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
(R)-(+)-Citronellal ((+)-Citronellal) Cat. No.: HY-111664
(R)-(+)-Citronellal, isolated from citrus,lavender and eucalyptus oils, is a monoterpenoidand main component of citronellal oil with adistinct lemon scent. A flavouring agent. Used forinsect repellent and antifungal properties.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
(R)-Citronellol (D-Citronellol; (R)-(+)-β-Citronellol) Cat. No.: HY-124257
(R)-Citronellol (D-Citronellol) is an alcoholicmonoterpene found in geranium essential oil.(R)-Citronellol inhibits degranulation of mastcells and does not affect caffeine bitternessperception.
Purity: >98%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
(Rac)-β-Chamigrenic acidCat. No.: HY-N7606
(Rac)-β-Chamigrenic acid is a racemate ofβ-Chamigrenic acid. β-Chamigrenic acid is ansesquiterpenoid isolated from .S.chinensis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg
(S)-(−)-Perillyl alcoholCat. No.: HY-116514
(S)-(−)-Perillyl alcohol is a monoterpene found inlavender, inhibits farnesylation of Ras,upregulates the mannose-6-phosphate receptor andinduces . Anti-cancer activity.apoptosis
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
(S)-(-)-Citronellal ((-)-Citronellal) Cat. No.: HY-111664A
(S)-(-)-Citronellal ((-)-Citronellal) is amonoterpenoid compound found in Corymbia
and essential oils.citriodora Cymbopogon nardus
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
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1,4-CineoleCat. No.: HY-N7117
1,4-Cineole is a widely distributed, natural,oxygenated monoterpene. 1,4-Cineole, present ineucalyptus oil, activates both human andTRPM8human .TRPA1
Purity: >95.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
10-Deacetylbaccatin IIICat. No.: HY-16565
10-Deacetylbaccatin-III is an intermediate fortaxol analog preparations. IC50 value: Target:Taxols have exhibit antitumor agents. Several ofthese taxols can be synthesized from 10-Deacetylbaccatin-III.
Purity: 95.05%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg, 200 mg, 500 mg
11-oxo-mogroside VCat. No.: HY-N0501
11-oxo-mogroside V is a natural sweetener,isolated from the fruits of Momordica
, exhibits strong antioxidant activity.grosvenori
Purity: 99.69%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
11-Oxomogroside IIeCat. No.: HY-N6852
11-Oxomogroside IIe is a triterpene glycosideisolated from .Siraitia grosvenori
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
11-Keto-beta-boswellic acid (11-Keto-β-boswellic acid) Cat. No.: HY-N2056
11-Keto-beta-boswellic acid (11-Keto-β-boswellicacid) is a pentacyclic triterpenic acid of theoleogum resin from the bark of the Boswellia
tree, popularly known as IndianserrateFrankincense.
Purity: 99.96%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
11-Oxomogroside IIICat. No.: HY-N6921
11-Oxomogroside III is a cucurbitane triterpeneglycoside isolated from in Siraitia grosvenoriifruits.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
12-Hydroxyganoderic Acid DCat. No.: HY-N7021
12-Hydroxyganoderic Acid D is a triterpenoidextracted from .Ganoderma lucidum
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
14-Deoxy-11,12-didehydroandrographolide (14-dehydro Andrographolide; AP10) Cat. No.: HY-N1490
14-Deoxy-11,12-didehydroandrographolide is ananalogue of Andrographolide that can be isolatedfrom .A. paniculata14-Deoxy-11,12-didehydroandrographolide inhibits
activation.NF-κB
Purity: 99.55%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg, 25 mg
15-Acetyl-deoxynivalenolCat. No.: HY-N6683
15-Acetyl-deoxynivalenol is a highly toxictrichothecene found in cereals, and a metaboliteof deoxynivalenol, exhibits toxicity to HepG2cells.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
16α-Hydroxydehydrotrametenolic acid (3β,16α-Dihydroxylanosta-7,9(11),24-trien-21-oic acid) Cat. No.: HY-N2990
16α-Hydroxydehydrotrametenolic acid is atriterpene Acid in fermented mycelia of ediblefungus .Poria cocos
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
4 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
18β-Glycyrrhetinic acidCat. No.: HY-N0180
18β-Glycyrrhetinic acid is the major bioactivecomponent of Glycyrrhizae Radix and possessesanti-ulcerative, anti-inflammatory andantiproliferative properties.
Purity: 99.63%Clinical Data: LaunchedSize: 10 mM × 1 mL, 500 mg, 5 g
2,2'-Anhydrouridine (2,2'-Cyclouridine; O2,2'-Cyclouridine) Cat. No.: HY-W012313
2,2'-Anhydrouridine is used for anticancer andantiviral research.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
20(R)-Ginsenoside Rg2Cat. No.: HY-N2039
20(R)-Ginsenoside Rg2, isolated from Ginseng stemsand leaves, shows inhibitory effects on lungcancer NCI-H1650 cells. Anti-cancer activities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
20(R)-Ginsenoside Rg3 (20(R)-Propanaxadiol; R-ginsenoside Rg3) Cat. No.: HY-N1376
20(R)-ginsenoside Rg3 (20(R)-Propanaxadiol), oneof the active compounds present in ginseng root,has a potent angiosuppressive and antitumoractivities.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
20(R)-Ginsenoside Rh2Cat. No.: HY-N1401
20(R)-Ginsenoside Rh2, a matrix inhibitor, acts as ametalloproteinase (MMP)
cell antiproliferator. It has anticancer effectsvia blocking cell proliferation and causing G1phase arrest.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
20(R)-Notoginsenoside R2Cat. No.: HY-N2049
20(R)-Notoginsenoside R2 is an isolatednotoginsenoside from .Panax notoginseng
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
20(S),24(R)-OcotillolCat. No.: HY-N6262
20(S),24(R)-Ocotillol is isolated from Panax.ginseng
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
20(S)-Ginsenoside Rg3 (20(S)-Propanaxadiol; S-ginsenoside Rg3) Cat. No.: HY-N0603
20(S)-Ginsenoside Rg3 is the main component of Redginseng. Ginsenoside Rg3 inhibits andNa+
channel with IC s of 32.2±4.5 and 32.6±2.2hKv1.4 50
μM, respectively. 20(S)-Ginsenoside Rg3 alsoinhibits levels, activity, and Aβ NF-κB COX-2expression.
Purity: 98.10%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
20-DeoxyingenolCat. No.: HY-N0866
20-Deoxyingenol is a natural compound.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
20-Hydroxyganoderic Acid GCat. No.: HY-N7018
20-Hydroxyganoderic Acid G is a lanostanetriterpenoid obtained from the EtOH extract offruiting bodies of the .Ganoderma curtisii20-Hydroxyganoderic Acid G inhibits BV-2 microgliacells activated by LPS with an IC of 21.33 μM.50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
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20-O-Acetylingenol-3-angelate (Euphorbia factor Pe1) Cat. No.: HY-N0868
20-O-Acetylingenol-3-angelate is a naturalcompound.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
21-O-TigloylgymnemageninCat. No.: HY-N2275
21-O-Tigloylgymnemagenin (Compound 7) is aacylated triterpenes isolated from Gymnema
.sylvestre
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
23-Hydroxylongispinogenin (12-Oleanene-3β,16β,23,28-tetrol;
3β,16β-12-Oleanene-3, 16,23,28-tetrol) Cat. No.: HY-N2274
23-Hydroxylongispinogenin(12-Oleanene-3β,16β,23,28-tetrol) is extractedfrom Klatt. Lysimachia heterogenea Lysimachia
Klatt is a perennial herb, which isheterogeneaused as a folk medicine in subduing swelling anddetoxicating in China.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
25-O-Methylalisol ACat. No.: HY-N6993
25-O-Methylalisol A is a protostane triterpenoidsisolated from .Alisma orientale
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
26-DeoxycimicifugosideCat. No.: HY-N5088
26-Deoxycimicifugoside is a triterpene xylosidesisolated from .Cimicifuga racemosa
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
27-DeoxyacteinCat. No.: HY-N6264
27-Deoxyactein is a constituent isolated from, prevents TCDD-inducedCimicifuga racemosa
osteoblasts damage. 27-Deoxyactein inhibitsincreased AhR, CYP1A1 and ERK levels.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
28-Demethyl-β-amyrone (28-Norolean-12-en-3-one) Cat. No.: HY-N7003
28-Demethyl-β-amyrone (28-Norolean-12-en-3-one) isone of the main triterpenes from Pistacia lentiscusvar. Chia. 28-Demethyl-β-amyrone is an antitoxinand can effectively for the toxic effects ofStaphylococcal enterotoxins (SEs).
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
3,29-Dibenzoyl rarounitriolCat. No.: HY-N0357
3,29-Dibenzoyl rarounitriol is one major bioactivecompound of multiflorane triterpene esters
, can be chosen as theTrichosanthes kirilowiimarker for quantitation of Trichosanthes
.kirilowii
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
3,29-O-Dibenzoyloxykarounidiol (Karounidiol dibenzoate) Cat. No.: HY-N7691
3,29-O-Dibenzoyloxykarounidiol (Karounidioldibenzoate) is a triterpene benzoate isolated fromthe fruit of .Momordica grosvenori
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg
3-Acetyl-beta-boswellic acidCat. No.: HY-N2075
3-Acetyl-beta-boswellic acid is a boswellic acidisolated from gum resin.Boswellia serrata
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
6 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
3-CareneCat. No.: HY-N6663
3-Carene is a bicyclic monoterpene in essentialoils extracted from pine trees. 3-Carene inhibitsnociceptive stimulus-induced inflammatoryinfiltrates and COX-2 overexpression, and withantinociceptive effect.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
3-Dehydrotrametenolic acidCat. No.: HY-N2177
3-Dehydrotrametenolic acid, isolated from thesclerotium of , is a Poria cocos lactate dehydrogenase
inhibitor. 3-Dehydrotrametenolic acid(LDH)promotes adipocyte differentiation and actsin vitroas an insulin sensitizer .in vivo
Purity: >99.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
3-Epioleanolic acidCat. No.: HY-N4290
3-Epioleanolic acid is an active component of Linn, with anti-inflammatoryVerbena officinalis
activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
3-Epiursolic AcidCat. No.: HY-N4289
3-Epiursolic Acid is a triterpenoid isolated fromMyrtaceae, acts as a competitive inhibitor of
(IC , 6.5 μM; , 19.5 μM), with nocathepsin L IC50 Ki
obvious effect on cathepsin B.
Purity: 99.20%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
3-O-Acetyl-16α-hydroxytrametenolic acidCat. No.: HY-N2994
3-O-Acetyl-16α-hydroxytrametenolic acid (Compound3) is a triterpene found in , withPoria cocosanti-oxidant and anti-cancer activity.
Purity: 99.23%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg
3-O-Beta-D-GlucopyranosylplatycodigeninCat. No.: HY-N3523
3-O-Beta-D-Glucopyranosylplatycodigenin is anoleanane-type triterpenoid isolated from roots of
.Platycodon grandiflorum3-O-Beta-D-Glucopyranosylplatycodigenin exhibitsanti-proliferative activities against HSC-T6 cellline with an IC of 13.36 μM.50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
3-Oxo-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-
lactone Cat. No.: HY-N4162
3-Oxo-21α-methoxy-24,25,26,27-tetranortirucall-7-ene-23(21)-lactone is a cytotoxic tirucallane C26triterpenoid isolated from the stem barks of
.Aphanamixis grandifolia
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
31-NorlanostenolCat. No.: HY-N7267
31-Norlanostenol is a triterpenic compoundisolated from the latex of Euphorbia
. 31-Norlanostenol can act asofficinarumefficient insect growth regulator on S. frugiperdaand .Tenebrio molitor
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
3α-HydroxymogrolCat. No.: HY-N6913
3α-Hydroxymogrol is a triterpenoid isolated from Swingle, acts as a potentSiraitia grosvenorii
activator, and enhances AMPKAMPKphosphorylation.
Purity: 98.47%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
4-Aza-Oleanolic acid methyl esterCat. No.: HY-18005
4-Aza-Oleanolic acid methyl ester is a triterpenicderivative.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
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5,15-Diacetyl-3-benzoyllathyrol (Euphorbia factor L3) Cat. No.: HY-N0562
5,15-Diacetyl-3-benzoyllathyrol is one of thelathyrane diterpenoids, that has anti-canceractivity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg, 10 mg
5,6-Didehydroginsenoside RdCat. No.: HY-N4263
5,6-Didehydroginsenoside Rd is a dammarane-typesaponin isolated from the dried roots of Panax
.notoginseng
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
6'-O-beta-D-GlucosylgentiopicrosideCat. No.: HY-N2100
6'-O-beta-D-Glucosylgentiopicroside is asecoiridoid isolated from the roots of G.
. 6'-O-beta-D-Glucosylgentiopicrosidestramineastrongly suppressesN-formyl-methionyl-leucyl-phenylalanine(fMLP)-induced superoxide generation.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
6'-O-Cinnamoyl harpagideCat. No.: HY-N4221
6'-O-Cinnamoyl harpagide is an iridoid glycosideisolated from the roots of .Scrophularia ningpoensis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
7-epi-Taxol (7-epi-Paclitaxel) Cat. No.: HY-N0227
7-epi-Taxol is an active metabolite of taxol, withactivity comparable to that of taxol against cellreplication, promoting bundlemicrotubuleformation and against microtubuledepolymerization.
Purity: 99.75%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
7-O-Geranylscopoletin (7-Geranyloxy-6-methoxycoumarin) Cat. No.: HY-N2746
7-O-Geranylscopoletin is a coumarin from the rootof . Various parts of thisAtalantia monophyllaplant have been used for folk medicine for severalpurposes such as chronic rheumatism, paralysis,antispasmodic, stimulant and hemiplegia.
Purity: >97.0%Clinical Data: No Development ReportedSize: 1 mg
7-O-Methyl morronisideCat. No.: HY-N6008
7-O-Methyl morroniside is an iridoid glycoside(IG) extracted from fructus, usedCornus officinalisin many traditional Chinese medicines.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
7-O-Methylaloeresin ACat. No.: HY-N2214
7-O-Methylaloeresin A is 5-methylchromoneglycoside isolated from Commiphora socotrana(Burseraceae).
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
7-xylosyltaxol (7-Xylosylpaclitaxel; Taxol-7-xyloside) Cat. No.: HY-77574
7-xylosyltaxol(Taxol-7-xyloside) is a taxol(Paclitaxel) derivative; Paclitaxel binds totubulin and inhibits the disassembly ofmicrotubules.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
7beta-HydroxylathyrolCat. No.: HY-N1484
7beta-Hydroxylathyrol is a natural product.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
8 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
8(14)-Abietenic acidCat. No.: HY-133615
8(14)-Abietenic acid is an abietane diterpenoid.Abietenic acid is racemic of 8(14)-Abietenic acid.Abietenic acid acts as a PPARα/γ dual activator.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
8-Epidiosbulbin E acetateCat. No.: HY-N7047
8-Epidiosbulbin E acetate, a furanoid, is abundantin . 8-Epidiosbulbin E acetateDioscorea bulbifera L.exhibits broad-spectrum plasmid-curing activityagainst multidrug-resistant (MDR) bacteria.8-Epidiosbulbin E acetate induces liver injury inmice.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg, 10 mg, 25 mg
8-O-AcetylharpagideCat. No.: HY-N0757
8-O-Acetylharpagide is an iridoid isolated from with antitumoral, antiviral,Ajuga reptans
antibacterial, and anti-inflammatory activities.8-O-Acetylharpagide also has a biological activityon isolated smooth muscle preparations from guineapig.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
9-cis-RetinalCat. No.: HY-W009310
9-cis-Retinal is a natural retinoid. Dietary9-cis-β-carotene generates 9-cis-retinoids viacleavage into 9-cis-retinal. 9-cis Retinal bindsto cellular retinol-binding protein-I (CRBP-I) andCRBP-II with s of 8 nM and 5 nM, respectively.Kd
Purity: >99.0%Clinical Data: No Development ReportedSize: 1 mg
Abietic acidCat. No.: HY-N6871
Abietic acid, a diterpene isolated from Pimenta var. grissea, possessesracemosa
antiproliferative, antibacterial, and anti-obesityproperties. Abietic acid inhibits lipoxygenaseactivity for allergy treatment.
Purity: >81.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg
Acanthopanaxoside BCat. No.: HY-N4135
Acanthopanaxoside B is a triterpenoid saponinisolated from the leaves of .Acanthopanax senticosus
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg
AcevaltrateCat. No.: HY-N2070
Acevaltrate, isolated from Valeriana, inhibits the /glechomifolia Na+ K -ATPase+
activity in the rat kidney and brain hemisphereswith s of 22.8±1.1 μM and 42.3±1.0 μM,IC50
respectively.
Purity: 99.56%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
ActeinCat. No.: HY-N6872
Actein is a triterpene glycoside isolated from therhizomes of . ActeinCimicifuga foetidasuppresses cell proliferation, induces autophagyand through promoting apoptosis ROS/JNKactivation, and blunting pathway in humanAKTbladder cancer. Actein has little toxicity .in vivo
Purity: 98.58%Clinical Data: No Development ReportedSize: 5 mg
Agnuside (Agnoside) Cat. No.: HY-N2518
Agnuside is a compound isolated from ,Vitex negundodown-regulates pro-inflammatory mediators PGE2and , and reduces the expression ofLTB4cytokines, with anti-arthritic activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
AjugolCat. No.: HY-N0914
Ajugol is an iridoid glycoside that can beisolated from .Sideritis germanicopolitanaAjugol has anti-protozoal activity againt
with an IC of 31.8Trypanosoma b. rhodesiense 50
μg/mL.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
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AKBA (Acetyl-11-keto-β-boswellic acid) Cat. No.: HY-N0892
AKBA (Acetyl-11-keto-β-boswellic acid) is anactive triterpenoid compound from the extract ofBoswellia serrate and a novel Nrf2 activator.
Purity: 99.71%Clinical Data: Phase 2Size: 10 mM × 1 mL, 5 mg, 10 mg
Alantolactone ((+)-Alantolactone; Alant camphor; Inula camphor) Cat. No.: HY-N0038
Alantolactone is a selective inhibitor,STAT3with potent anticancer activity. Alantolactoneinduces apoptosis in cancer.
Purity: 99.94%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
AlbiflorinCat. No.: HY-N0037
Albiflorin is a major constituent contained inpeony root; possesses therapeutic potential forneurodegenerative diseases.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Alismoxide ((+)-Alismoxide) Cat. No.: HY-N0426
Alismoxide is a natural product.
Purity: 95.27%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg
Alisol BCat. No.: HY-N0805A
Alisol B is a potentially novel therapeuticcompound for bone disorders by targeting thedifferentiation of osteoclasts as well as theirfunctions.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Alisol B 23-acetate (23-Acetylalismol B; 23-O-Acetylalisol B;
Alisol B monoacetate) Cat. No.: HY-N0805
Alisol B 23-acetate (23-Acetylalismol B), anatural triterpenoid, produces protective effectsagainst EE-induced cholestasis, due toFXR-mediated gene regulation. IC50 Value: Target:Anti-hepatotoxic natural product.
Purity: 99.84%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Alisol C 23-acetate (23-O-Acetylalisol C; Alisol C monoacetate) Cat. No.: HY-N0856
Alisol C 23-acetate, a natural product extractedfrom Alisma orientale, can significantly andstrongly inhibit DTH response after oraladministration.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Alisol FCat. No.: HY-N0854
Alisol F is a triterpene isolated from Alisma, has immunosuppressive and anti-virusorientalis
functions. Alisol F exhibits inhibitory activityin vitro on hepatitis B virus (HBV) surfaceantigen (HBsAg) secretion of the HepG2.2.15 cellline with an IC of 0.6 μM.50
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Alisol G (Alisol-G; 25-Anhydroalisol A) Cat. No.: HY-N0855
Alisol G is a natural product extracted fromRhizoma Alismatis.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg
alpha-BisabololCat. No.: HY-121222
alpha-Bisabolol is a nontoxic sesquiterpenealcohol present in natural essential oil, withanticancer activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
10 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
alpha-Boswellic acid (α-Boswellic acid) Cat. No.: HY-N0611
alpha-Boswellic acid (α-Boswellic acid) is apentacyclic triterpene compound from extracts of
, has anticonvulsant and anti-cancerFrankincenseproperties.
Purity: 98.40%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
alpha-Cyperone (α-Cyperone; (+)-α-Cyperone) Cat. No.: HY-N0710
alpha-Cyperone (α-Cyperone) is associated with thedown-regulation of COX-2, IL-6, Nck-2, Cdc42 andRac1, resulting in reduction of inflammation,which would be highly beneficial for treatment ofinflammatory diseases such as AD.
Purity: 99.12%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 25 mg, 50 mg
alpha-Hederin (α-Hederin) Cat. No.: HY-N0255
alpha-Hederin (α-Hederin) is a water-solublepentacyclic triterpenoid saponin, possessingseveral biological properties such asantispasmodic, moliscicidic, anthelmithic andinhibiting cell proliferation.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
AmarogentinCat. No.: HY-N2447
Amarogentin is a secoiridoid glycoside that ismainly extracted from and Swertia Gentianaroots. Amarogentin exhibits many biologicaleffects, including anti-oxidative, anti-tumour,and anti-diabetic activities.
Purity: 98.96%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
AmbroxideCat. No.: HY-N1384
Ambroxide is a naturally occurring terpenoid.Ambroxide is one of the key constituents ofambergris.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ammonium glycyrrhizinate (Monoammonium glycyrrhizinate) Cat. No.: HY-N0184B
Ammonium glycyrrhizinate is a triterpenoidsaponin, acting as a direct antagonist,HMGB1with anti-inflammatory anti-tumor, anti-diabeticactivities.
Purity: >98%Clinical Data: LaunchedSize: 1 mg, 5 mg
Andrographolide (Andrographis) Cat. No.: HY-N0191
Andrographolide is a inhibitor, whichNF-κBinhibits NF-κB activation through covalentmodification of a cysteine residue on inp50endothelial cells without affecting IκBαdegradation or p50/p65 nuclear translocation.Andrographolide has antiviral effects.
Purity: 98.57%Clinical Data: LaunchedSize: 100 mg, 500 mg
AndropanosideCat. No.: HY-N2868
Andropanoside is a natural product isolated andpurified from the herbs of .Andrographis paniculata
possesses a protectiveAndrographis paniculataactivity against various liver disorders.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Araloside A (Chikusetsusaponin IV) Cat. No.: HY-N2115
Araloside A (Chikusetsusaponin IV) is a componentof , with low- -inhibitoryPanax japonicus reninactivity, with an of 77.4 μM.IC50
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Araloside V (Congmunoside V) Cat. No.: HY-N6970
Araloside V (Congmunoside V) is a triterpenoidsaponin isolated from .Aralia elata
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
www.MedChemExpress.com 11
Araloside VII (Congmunoside VII) Cat. No.: HY-N2002
Araloside VII (Congmunoside VII) is a saponinisolated from leaves of .Aralias elate
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Araloside XCat. No.: HY-N2001
Araloside X (Congmunoside X) is a triterpenoidsaponin isolated from .Aralia elata
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Ardisiacrispin A (Deglucocyclamin; LTS-4; Saxifragifolin B) Cat. No.: HY-N0206
Ardisiacrispin A (Deglucocyclamin) is a commontriterpenoid saponin from Ardisia species.Ardisiacrispin A has similar biological propertieswith some triterpenoid saponins in A.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Arglabin ((+)-Arglabin) Cat. No.: HY-16059
Arglabin ((+)-Arglabin), a natural productisolated from , is a Artemisia glabella NLRP3
inhibitor. Arglabin showsinflammasomeanti-inflammatory and antitumor activities.
Purity: 99.17%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
ArjunetinCat. No.: HY-N7592
Arjunetin, isolated from , isTerminalia arjunaan insect feeding-deterrent and growth inhibitor.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg
ArjungeninCat. No.: HY-N4294
Arjungenin, a triterpene isolated from, is an insectTerminalia arjuna
feeding-deterrent and growth inhibitor.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Arnicolide DCat. No.: HY-N6843
Arnicolide D is a sesquiterpene lactone isolatedfrom . Arnicolide D modulatesCentipeda minimathe cell cycle, activates the signalingcaspasepathway and inhibits the andPI3K/AKT/mTOR
signaling pathways.STAT3
Purity: >99.0%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
ArnicolideCCat. No.: HY-N6842
ArnicolideC is a sesquiterpene lactone isolated. ArnicolideC exertes aCentipeda minima
cytotoxic effect on the panel of Nasopharyngealcarcinoma (NPC) cells, significantly inhibitingcell growth in a dose- and time- dependent manner.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
ArnidiolCat. No.: HY-N4165
Arnidiol is a pentacyclic triterpene isolated from F.Barleria Longiflora Linn
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Artemether (Dihydroqinghaosu methyl ether; Dihydroartemisinin
methyl ether; SM224) Cat. No.: HY-N0402
Artemether is an antimalarial for the treatment ofresistant strains of falciparum malaria. Target:Antiparasitic Artemether is an antimalarial agentused to treat acute uncomplicated malaria. It isadministered in combination with lumefantrine forimproved efficacy.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg
12 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Artemisic acid (Qing Hao acid; Artemisinic acid; Arteannuic acid) Cat. No.: HY-N1984
Artemisinic acid (Qing Hao acid), an amorphanesesquiterpene isolated from L.Artemisia annua
Purity: 99.88%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
Artemisinin (Qinghaosu; NSC 369397) Cat. No.: HY-B0094
Artemisinin (Qinghaosu), a sesquiterpene lactone,is an drug isolated from theanti-malarialaerial parts of L. plants.Artemisia annuaArtemisinin inhibits AKT signaling pathway bydecreasing in a dose-dependent manner.pAKT
Purity: 99.03%Clinical Data: LaunchedSize: 10 mM × 1 mL, 200 mg, 500 mg
Asiatic acidCat. No.: HY-N0194
Asiatic acid, a pentacyclic triterpene found in, induces apoptosis in melanomaCentella asiatica
cells. Asiatic acid has the potential for skincancer treatment. Asiatic acid also hasanti-inflammatory activities.
Purity: 99.47%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
AsiaticosideCat. No.: HY-N0439
Asiaticoside, a trisaccaride triterpene from, suppresses Centella asiatica TGF-β/Smad
signaling through inducing Smad7 and inhibitingTGF-βRI and TGF-βRII in keloid fibroblasts;Asiaticoside shows antioxidant, anti-inflammatory,and anti-ulcer properties.
Purity: 99.84%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
Asiaticoside BCat. No.: HY-N5052
Asiaticoside B is a triterpene glycoside isolatedfrom , with anti-cancer activity.Actaea asiatica
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Asperosaponin VICat. No.: HY-N0265
Asperosaponin VI, A saponin component from Dipsacus wall, induces osteoblast differentiationasper
through BMP2/p38 and ERK1/2 pathway.
Purity: 98.73%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
AsperulosideCat. No.: HY-N1382
Asperuloside is an iridoid isolated from Hedyotis, with anti-inflammatory activity.diffusa
Asperuloside inhibits inducible nitric oxidesynthase ( ), suppresses NF-κB and MAPKiNOSsignaling pathways.
Purity: 99.69%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
AstaxanthinCat. No.: HY-B2163
Astaxanthin, a red dietary carotenoid isolatedfrom , is a modulator ofHaematococcus pluvialis
and a potent antioxidant withPPARγantiproliferative, neuroprotective andanti-inflammatory activity.
Purity: >98.0%Clinical Data: LaunchedSize: 5 mg, 10 mg
Astragaloside I (Astrasieversianin IV; Cyclosieversioside B) Cat. No.: HY-N0432
Astragaloside I is a natural product isolated fromAstragalus.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Astragaloside II (Astrasieversianin VIII) Cat. No.: HY-N0433
Astragaloside II is a natural isolated fromAstragalus. IC50 value: Target: In vitro: In vivo:The developed and validated method has beensuccessfully applied to the quantification andpharmacokinetic study of AST II in rats afterintravenous and oral administration of AST II.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
www.MedChemExpress.com 13
Astragaloside IIICat. No.: HY-N0434
Astragaloside III is a natural product isolatedfrom Astragalus.
Purity: 98.89%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Astragaloside IVCat. No.: HY-N0431
Astragaloside IV, an active component isolatedfrom , suppresses theAstragalus membranaceusactivation of and , and downregulatesERK1/2 JNKmatrix metalloproteases in(MMP)-2, (MMP)-9MDA-MB-231 breast cancer cells.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
Atractylenolide ICat. No.: HY-N0201
Atractylenolide I is a sesquiterpene derived fromthe rhizome of Atractylodes macrocephala,possesses diverse bioactivities, such asneuroprotective, anti-allergic, anti-inflammatoryand anticancer properties.
Purity: 99.08%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
Atractylenolide II (Asterolide) Cat. No.: HY-N0202
Atractylenolide II is a sesquiterpene compoundisolated from the dried rhizome of Atractylodesmacrocephala (Baizhu in Chinese);anti-proliferative activity.
Purity: 99.91%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Atractylenolide III (ICodonolactone; 8β-Hydroxyasterolide) Cat. No.: HY-N0203
Atractylenolide III is a major component ofAtractylodes rhizome can induce apoptosis of thelung carcinoma cells.
Purity: 99.91%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Atractylone (Atractylon) Cat. No.: HY-N2095
Atractylone (Atractylon) is a sesquiterpenoidextracted from . AtractyloneAtractylodis Rhizoma(Atractylon) alleviates influenza A virus(IAV)-induced lung injury via regulating the TLR7signaling pathway, and acts as a promising agentfor IAV treatment.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Atractyloside ACat. No.: HY-N0237
Atractyloside A is a natural TCM referencecompound.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
Atractyloside potassium saltCat. No.: HY-N1462
Atractyloside potassium salt is a toxicditerpenoid glycoside isolated from the fruits of
. Atractyloside potassiumXanthium sibiricumsalt is a powerful and specific inhibitor ofmitochondrial .ADP/ATP transport
Purity: 99.93%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 500 μg, 1 mg, 5 mg, 10 mg
AucubinCat. No.: HY-N0664
Aucubin is an iridoid glycoside with a wide rangeof biological activities, includinganti-inflammatory, anti-microbial, anti-algesic aswell as anti-tumor activities.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Bacopaside IICat. No.: HY-N6016
Bacopaside II, an extract from the medicinal herb, blocks the Bacopa monnieri Aquaporin-1 (AQP1)
water channel and impairs migration of cells thatexpress AQP1. Bacopaside II induces cell cyclearrest and apoptosis.
Purity: 98.69%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
14 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Bacopaside VCat. No.: HY-N4295
Bacopaside V is a bioactive triterpenoid glycosideof , a herb having confirmedBacopa monnieranervine tonic activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Bacoside A3Cat. No.: HY-N5064
Bacoside A3, a triterpenoid saponin, is one of themajor active constituents in .Bacopa monnieriBacoside A3 has neuroprotective activity.
Purity: 98.47%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Bakkenolide BCat. No.: HY-N7292
Bakkenolide B is isolated from petasites japonicasleaves and has anti-allergic andanti-inflammatory effects. Bakkenolide B can beused for the study of asthma.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Bakuchiol ((S)-(+)-Bakuchiol) Cat. No.: HY-N0235
Bakuchiol is a phytoestrogen isolated from theseeds of Psoralea corylifolia L; has anti-tumoreffects.
Purity: 99.25%Clinical Data: Phase 2Size: 10 mM × 1 mL, 5 mg, 10 mg
Barlerin (8-O-Acetyl shanzhiside methyl ester) Cat. No.: HY-N0758
Barlerin (8-O-Acetyl shanzhiside methyl ester) isan iridoid glucoside isolated from the leaves of
, a Chinese folkLamiophlomis rotata Kudomedicinal plant in Xi-zang. Barlerin (8-O-Acetylshanzhiside methyl ester) could inhibt .NF-κB
Purity: 99.82%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 25 mg
BayogeninCat. No.: HY-N1932
Bayogenin is an alfalfa saponin, shows moderatepotency of glycogen phosphorylase inhibition.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Bayogenin 3-O-β-D-glucopyranosideCat. No.: HY-N2601
Bayogenin 3-O-β-D-glucopyranoside, a triterpenoidsaponin isolated from , possessesPolygala japonicaanti-inflammatory activities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Beesioside QCat. No.: HY-125686
Beesioside Q is a oleanolic acid triterpenesaponin isolated from the rhizome of Beesia
(Maxim.) Ulbr.calthaefolia
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
BenzoyloxypaeoniflorinCat. No.: HY-N2101
Benzoyloxypaeoniflorin, isolated from the root of, is a inhibitorPaeonia suffruticosa tyrosinase
against mushroom tyrosinase with of 0.453 mM.IC50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
BenzoylpaeoniflorinCat. No.: HY-N0852
Benzoylpaeoniflorin is a natural product; maytreat coronary heart disease by decreasingapoptosis.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
www.MedChemExpress.com 15
Bernardioside ACat. No.: HY-N2606
Bernardioside A is a triterpenoid saponin isolatedfrom .Bellis bernardii
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Beta-EudesmolCat. No.: HY-N6018
Beta-Eudesmol is a natural oxygenatedsesquiterpene, activates , with an hTRPA1 EC50
of 32.5 μM. Beta-Eudesmol increases appetitethrough TRPA1.
Purity: 96.54%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
Betulin (Trochol) Cat. No.: HY-N0083
Betulin (Trochol), is a sterol regulatoryelement-binding protein ( ) inhibitor with anSREBP
of 14.5 μM in K562 cell line.IC50
Purity: >98.0%Clinical Data: No Development ReportedSize: 50 mg, 100 mg, 200 mg
Betulinaldehyde (Betulinic aldehyde; Betunal) Cat. No.: HY-N0084
Betulinaldehyde(Betunal) belongs to pentacyclictriterpenoids and was reported to exhibitantimicrobial activities against bacteria andfungi, including S. aureus.
Purity: 98.56%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
Betulinic acid (Lupatic acid; Betulic acid) Cat. No.: HY-10529
Betulinic acid is a natural pentacyclictriterpenoid, acts as a eukaryotic
inhibitor, with an of 5 μM,topoisomerase I IC50
and possesses anti-HIV, anti-malarial,anti-inflammatory and anti-tumor properties.Betulinic acid acts as a new activator of .NF-kB
Purity: >98.0%Clinical Data: Phase 2Size: 10 mM × 1 mL, 100 mg, 200 mg, 500 mg
Betulinic acid methyl ester (Methyl betulinate) Cat. No.: HY-N6587
Betulinic acid methyl ester, a betulinic acidderivative, possesses antiprotozoal activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Betulonic acid (Betunolic acid; Liquidambaric acid; (+)-Betulonic acid) Cat. No.: HY-N1451
Betulonic acid belongs to the pentacyclictriterpenic derivative class, has antitumoractivities. In vitro: BEA-NP is found overthree-times more permeable than that solubilizedby DMSO in Caco-2 cell monocultures.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Bevirimat (PA-457; MPC-4326; YK FH312) Cat. No.: HY-N0842
Bevirimat (PA-457; MPC-4326; YK FH312) is ananti-HIV drug derived from a betulinic acid-likecompound; is believed to inhibit HIV by a novelmechanism, so-called maturation inhibition.
Purity: >98.0%Clinical Data: Phase 2Size: 10 mM × 1 mL, 5 mg, 10 mg
Bilobalide ((-)-Bilobalide) Cat. No.: HY-N0076
Bilobalide is a biologically active terpenictrilactone present in Ginkgo biloba. An increasingnumber of studies have demonstrated itsneuroprotective effects.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
BisabolangeloneCat. No.: HY-N4233
Bisabolangelone, a sesquiterpene derivative, isisolated from the roots of Osterici Radix.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
16 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
BlininCat. No.: HY-N0463
Blinin is a neoclerodane diterpene, isolated fromthe whole plant of .Conyza blinii
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Bonducellpin DCat. No.: HY-N2949
Bonducellpin D is a furanoditerpenoid lactoneisolated from . Bonducellpin DCaesalpinia minaxexhibits broad-spectrum inhibition potentialagainst and SARS-CoV Mpro MERS-CoV
, with an of 467.11 and 284.86 nM,Mpro Ki
respectively.
Purity: >98.0%Clinical Data: No Development ReportedSize: 1 mg
Brevilin ACat. No.: HY-N2959
Brevilin A is a sesquiterpene lactone isolatedfrom with anti-tumor activity.Centipeda minimaBrevilin A is a selective inhibitor of JAK-STATsignal pathway by attenuating the JAKs activityand blocking STAT3 signaling ( = 10.6 µM) inIC50
Cancer Cells.
Purity: 99.77%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Britannilactone (Desacetylinulicin) Cat. No.: HY-N0895
Britannilactone(Desacetylinulicin) is a methanolextract of the dried flower of Inula britannica L.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
BritanninCat. No.: HY-N3005
Britannin, isolated from , is aInula aucherianasesquiterpene lactone. Britannin induces apoptosisand by activating AMPK regulated by ROSautophagyin liver cancer cells. Britannin hasanti-proliferative and anti-inflammatoryactivities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Brusatol (NSC 172924) Cat. No.: HY-19543
Brusatol (NSC 172924), isolated from the Brucea plant, inhibits .javanica Nrf2
Purity: 99.89%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Buddlejasaponin IVbCat. No.: HY-N2138
Buddlejasaponin IVb (Compound 2), a triterpenesaponin isolated from Clinopodium chinense
, Compound 2 has hemostasis(Benth.) O. Kuntzeefficacy, shortens thrombin time (TT) by 20.6 %.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Caesalmin BCat. No.: HY-N2981
Caesalmin B is a furanoditerpenoid lactoneisolated from . Caesalmin BCaesalpinia minaxexhibits antiviral activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
CafestolCat. No.: HY-N6257
Cafestol, one of the major components of coffee,is a coffee-specific diterpene from. Cafestol is a
inhibitor for AP-1-targeted activity againstERK production and the mRNA expression ofPGE2
in LPS-activated RAW264.7cyclooxygenase (COX)-2cells.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Calenduloside ECat. No.: HY-N6850
Calenduloside E (CE) is a natural pentacyclictriterpenoid saponin extracted from .Aralia elataCalenduloside E (CE) has potent byanti-apoptotictargeting heat shock protein 90 ( ).Hsp90
Purity: 98.47%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
www.MedChemExpress.com 17
Camphor ((±)-Camphor) Cat. No.: HY-N0808
Camphor ((±)-Camphor) is a topical anti-infectiveand anti-pruritic and internally as a stimulantand carminative. However, Camphor is poisonouswhen ingested. Antiviral, antitussive, andanticancer activities. Camphor is a TRPV3agonist.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Canthaxanthin (E 161g; all-trans-Canthaxanthin) Cat. No.: HY-B1960
Canthaxanthin is a red-orange carotenoid withvarious biological activities, such asantioxidant, antitumor properties.
Purity: >95.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 50 mg, 100 mg
CarabroneCat. No.: HY-N5020
Carabrone is isolated from the fruits of , is a well-knownCarpesium abrotanoides
sesquiterpene and exhibits significantanti-bacterial and anti-tumor activities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Carboxyatractyloside (Gummiferin) Cat. No.: HY-N1502
Carboxyatractyloside is a toxic natural product,acts as an inhibitor of , inhibitsADP/ATP carriermitochondrial ADP/ATP transport.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Carboxyatractyloside dipotassium (Gummiferin dipotassium) Cat. No.: HY-N2522
Carboxyatractyloside dipotassium is a toxicnatural product, acts as an inhibitor of ADP/ATP
, inhibits mitochondrial ADP/ATP transport.carrier
Purity: 98.69%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Carnosic acidCat. No.: HY-N0644
Carnosic acid has demonstrated inhibition ofoxidative stress and inflammation, suppression ofcell proliferation, and antibacterial activity.
Purity: 99.53%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
CarvacrolCat. No.: HY-N0711
Carvacrol is a monoterpenoid phenol isolated fromLamiaceae family plants, with antioxidant,anti-inflammatory and anticancer properties.Carvacrol causes cell cycle arrest in G0/G1,downregulates , and Jagged-1, and inducesNotch-1
.apoptosis
Purity: 99.99%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
CarveolCat. No.: HY-W017370
Carveol is an endogenous metabolite.
Purity: >98%Clinical Data: No Development ReportedSize: 500 mg
Catalpol (Catalpinoside) Cat. No.: HY-N0820
Catalpol, an iridoid glycoside, hasneuroprotective, anti-inflammatory, andanti-hepatitis virus effects. IC50 Value: Target:neuroprotective, anti-inflammatory, andanti-hepatitis virus natural product.
Purity: 98.04%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
CaulophyllogeninCat. No.: HY-N7687
Caulophyllogenin is a triterpene saponin extractedfrom . Caulophyllogenin is aM. polimorphapartial agonist, with anPPARγ
of12.6μM. Caulophyllogenin can be usedEC50
for the research of type-2 diabetes, obesity,metabolic syndrome and inflammation.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg
18 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Cauloside CCat. No.: HY-N6919
Cauloside C is a triterpene glycoside isolatedfrom Max. Cauloside CCaulophyllum robustumexerts anti-inflammatory effects through theinhibition of expression of iNOS andproinflammatory cytokines.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Cauloside DCat. No.: HY-N6878
Cauloside D is a triterpene glycoside isolatedfrom Max. Cauloside DCaulophyllum robustumexerts anti-inflammatory effects through theinhibition of expression of iNOS andproinflammatory cytokines.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Cauloside FCat. No.: HY-N6265
Cauloside F is a triterpenoid saponin isolatedfrom .Clematis akebioides
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Ceanothic acid (Emmolic acid) Cat. No.: HY-N3558
Ceanothic acid (Emmolic acid) is a ring-Ahomologue of betulinic acid. Ceanothic acidinhibits OVCAR-3, HeLa, and FS-5 cells with thecell survival of 68%, 65%, and 81%, respectively.
Purity: >98.0%Clinical Data: No Development ReportedSize: 1 mg
Cedrol ((+)-Cedrol; α-Cedrol) Cat. No.: HY-N2071
Cedrol is a bioactive sesquiterpene, a potentcompetitive inhibitor of cytochrome P-450(CYP) enzymes. Cedrol inhibits CYP2B6-mediatedbupropion hydroxylase and CYP3A4-mediatedmidazolam hydroxylation with of 0.9 μM and 3.4Ki
μM, respectively.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Celosin ICat. No.: HY-N7026
Celosin I, an oleanane-type triterpenoid saponinisolated from the seeds of L, couldCelosia argenteabe used as chemical markers for the qualitycontrol of seeds.C. argentea
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
CephalomannineCat. No.: HY-77554
Cephalomannine is a Paclitaxel (HY-B0015)alkaloidal analog and isolated from most
species. Cephalomannine is an orallyCephalotaxusactive and can be used as aanti-tumor agentchemotherapy agent for cancer research.
Purity: 98.38%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Chikusetsusaponin Iva (Calenduloside F) Cat. No.: HY-N0818
Chikusetsusaponin IVa a major active ingredient oftriterpenoid saponins, exerts antithromboticeffects, including minor hemorrhagic events. Thisappears to be important for the development of newtherapeutic agents.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Chlorahololide CCat. No.: HY-N8404
Chlorahololide C, a lindenane sesquiterpenoiddimer, is isolated from .Chloranthus holostegiusChlorahololide C is a potent and selectivepotassium channel blocker, with an of 3.6 μM.IC50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
CimicifugosideCat. No.: HY-N7119
Cimicifugoside, a triterpenoid isolated from, is a novel specificCimicifuga simplex
inhibitor that displaysnucleoside transportsynergistic potentiation of methotrexatecytotoxicity.
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
www.MedChemExpress.com 19
CimigenolCat. No.: HY-N6988
Cimigenol is an active compound isolated from, with potent anti-tumor activity.Cimicifuga
Purity: 99.79%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Cimigenol-3-O-α-L-arabinosideCat. No.: HY-N2042
Cimigenol-3-O-α-L-arabinoside is a triterpenoidisolated from L.Cimicifuga foetida
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
CimigenosideCat. No.: HY-N2097
Cimigenoside is an active compound from genus.Cimicifuga
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Cimiracemoside C (Cimicifugoside M) Cat. No.: HY-N6971
Cimiracemoside C is an active component of, activates , hasCimicifuga racemosa AMPK
the potential activity against diabetes.
Purity: 99.55%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Cimiracemoside DCat. No.: HY-N0900
Cimiracemoside D is a natural product found inActaea racemosa with unknown details.
Purity: >99.0%Clinical Data: No Development ReportedSize: 5 mg
cis-Isolimonenol ((1S,4R)-p-Mentha-2,8-dien-1-ol) Cat. No.: HY-41094
cis-Isolimonenol ((1S,4R)-p-Mentha-2,8-dien-1-ol)is a chemical composition of essential oil.
Purity: >98%Clinical Data: No Development ReportedSize: 500 mg
cis-p-Menthan-1,8-diol (4-p-Menthan-1,8-diol) Cat. No.: HY-N4324
cis-p-Menthan-1,8-diol is a natural menthanemonoterpenoid.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
CitralCat. No.: HY-N7083
Citral is a monoterpene found in Cymbopogon essential oil, with antihyperalgesic,citratus
anti-nociceptive and anti-inflammatory effects.
Purity: >95.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Citronellol ((±)-Citronellol; (±)-β-Citronellol) Cat. No.: HY-W010201
Citronellol ((±)-Citronellol) is a monoterpene.Pelargonium capitatum
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Ciwujianoside BCat. No.: HY-N0307
Ciwujianoside B is isolated from Eleutherococcus leaf, is able to penetrate and work insenticosus
the brain after the oral administration.Ciwujianoside B significantly enhances objectrecognition memory.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
20 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Clinodiside ACat. No.: HY-N1371
Clinodiside A is isolated from the Chinesemedicinal herb .Clinopodium chinensis
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
ColumbinCat. No.: HY-N0389
Columbin is an orally active diterpenoidfuranolactone from , hasCalumbae radixanti-inflammatory and anti-trypanosomal effects.Columbin selectively inhibits ( =53.1COX-2 EC50
μM) over COX-1 (EC =327 μM).50
Purity: 98.86%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg
Continentalic acidCat. No.: HY-N6908
Continentalic acid from hasAralia continentalisminimum inhibitory concentrations (MICs) ofapproximately 8-16 µg/mL against ,S. aureusincluding the Methicillin susceptible
(MSSA) andStaphylococcus aureusMethicillin-resistant …Staphylococcus aureus
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Coronalolic acid (Coronalonic acid) Cat. No.: HY-N3625
Coronalolic acid, extract from the apical bud of Hutch, inhibits TNF-α-inducedGardenia sootepenesis
activity and production.NF-κB NO
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Corosolic acid (Colosolic acid) Cat. No.: HY-N0280
Corosolic acid (Colosolic acid) isolated from thefruit of Cratoegus pinnatifida var. psilosa, wasreported to have anticancer activity.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Costunolide ((+)-Costunolide; Costus lactone) Cat. No.: HY-N0036
Costunolide ((+)-Costunolide; Costus lactone) is abioactive sesquiterpene lactone, withantioxidative, anti-inflammatory, antiallergic,bone remodeling, neuroprotective, hair growthpromoting, anticancer, and antidiabeticproperties.
Purity: 99.84%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Crocin IICat. No.: HY-N0698
Crocin II is isolated from the fruit of Gardenia with antioxidant, anticancer, andjasminoides
antidepressant activity. Crocin II inhibits NOproduction with an value of 31.1 μM. CrocinIC50
II suppresses the expressions of protein and m-RNAof and .iNOS COX-2
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Cucurbitacin BCat. No.: HY-N0416
Cucurbitacin B belongs to a class of highlyoxidized tetracyclic triterpenoids; could represscancer cell progression.
Purity: 99.92%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg
Cucurbitacin DCat. No.: HY-N1986
Cucurbitacin D is an active component in Cucurbita, disrupts interactions between andtexana Hsp90
two co-chaperones, Cdc37 and p23. Cucurbitacin Dprevents Hsp90 client (Her2, Raf, Cdk6, pAkt)maturation without induction of the heat shockresponse. Anti-cancer activity.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
Cucurbitacin E (α-Elaterin; α-Elaterine) Cat. No.: HY-N0417
Cucurbitacin E is a natural compound which fromthe climbing stem of .Cucumic melo LCucurbitacin E significantly suppresses theactivity of the / complex.cyclin B1 CDC2
Purity: 99.92%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
www.MedChemExpress.com 21
Cucurbitacin I (Elatericin B; JSI-124; NSC-521777) Cat. No.: HY-N1405
Cucurbitacin I is a natural selective inhibitor of, with potent anti-cancer activity.JAK2/STAT3
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
Cucurbitacin IIa (Hemslecin A) Cat. No.: HY-N1988
Cucurbitacin IIa is a triterpene isolated from Diels, induces apoptosis ofHemsleya amalils
cancer cells, reduces expression of ,survivinreduces phospho-Histone H3 and increases cleavedPARP in cancer cells.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Cucurbitacin IIbCat. No.: HY-N1987
Cucurbitacin IIb is an active component isolatedfrom , induces Hemsleya amabilis apoptosiswith anti-inflammatory activity.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Cucurbitacin SCat. No.: HY-N0725
Cucurbitacin S is isolated from withcucurbitaceaeanticancer and anti-inflammatory activities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Curcumol ((-)-Curcumol) Cat. No.: HY-N0104
Curcumol ((-)-Curcumol), a bioactivesesquiterpenoid, possesses numerouspharmacological activities like anticancer,antimicrobial, antifungal, antiviral, andantiinflammatory.
Purity: 99.58%Clinical Data: Phase 3Size: 10 mM × 1 mL, 5 mg, 10 mg
Curdione ((+)-Curdione) Cat. No.: HY-N0353
Curdione, one of the major sesquiterpene compoundsfrom Rhizoma Curcumae, has been shown to exhibitmultiple bioactive properties.
Purity: 99.44%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
CurzereneCat. No.: HY-N1963
Curzerene is a sesquiterpene is isolated from therhizome of withCurculigo orchioides Gaertnanti-cancer activity. Curzerene inhibitsglutathione S-transferase A1 ( ) mRNA andGSTA1protein expression. Curzerene induces cell
.apoptosis
Purity: >97.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Cycloastragenol (Cyclogalagenin; Cyclogalegenin; Cyclogalegigenin) Cat. No.: HY-N0424
Cycloastragenol, a natural tetracyclictriterpenoid, was first identified when screeningAstragalus membranaceus extracts for activeingredients with antiaging properties.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
CynaropicrinCat. No.: HY-N2350
Cynaropicrin is a sesquiterpene lactone which caninhibit ( ) releasetumor necrosis factor TNF-αwith s of 8.24 and 3.18 μM for murine andIC50
human macrophage cells, respectively.
Purity: 97.40%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
CyperotundoneCat. No.: HY-N3004
Cyperotundone is a sesquiterpene isolated fromNagarmotha ( ).Cyperus rotundus
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
22 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
DaphyllosideCat. No.: HY-N6245
Daphylloside is an iridoid isolated from theaerial parts of .Galium verum
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DarutigenolCat. No.: HY-N3003
Darutigenol is an ent-pimarane-type diterpenoidisolated from .Siegesbecikia orientalis L.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DarutosideCat. No.: HY-N6028
Darutoside is a diterpenoid isolated fromSiegesbeckia.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Deapi-platycodin D3Cat. No.: HY-N3520
Deapi-platycodin D3 is a triterpenoid saponin fromthe roots of .Platycodon grandiflorum
Purity: 98.17%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Deapioplatycodin DCat. No.: HY-N0588
Deapioplatycodin D is a triterpenoid saponinisolated from , withPlatycodon grandiflorumanti-HCV activity.
Purity: 95.44%Clinical Data: No Development ReportedSize: 1 mg, 5 mg, 10 mg
Dehydroabietic acidCat. No.: HY-N6869
Dehydroabietic acid possesses antiviral activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
DehydroandrographolideCat. No.: HY-N0676
Dehydroandrographolide is extracted from herbalmedicine .Andrographis paniculata NeesDehydroandrographolide reduces oxidative stress inLPS-induced acute lung injury by inactivatingiNOS. Dehydroandrographolide has anti-infectiveactivity.
Purity: 99.93%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
Dehydroandrographolide succinateCat. No.: HY-N0677
Dehydroandrographolide succinate, extracted fromherbal medicine (Burm f)Andrographis paniculataNees, is widely used for the treatment of viralpneumonia and viral upper respiratory tractinfections because of its immunostimulatory,anti-infective and anti-inflammatory effect.
Purity: 99.88%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
Dehydroandrographolide succinate potassium sodium saltCat. No.: HY-N0677B
Dehydroandrographolide succinate (potassium sodiumsalt), extracted from herbal medicine Andrographis
(Burm f) Nees, is widely used for thepaniculatatreatment of viral pneumonia and viral upperrespiratory tract infections because of itsimmunostimulatory, anti-infective…
Purity: >98%Clinical Data: LaunchedSize: 5 mg, 10 mg, 20 mg
Dehydrocostus Lactone ((-)-Dehydrocostus lactone; Epiligulyl oxide) Cat. No.: HY-N0591
Dehydrocostus Lactone is a major sesquiterpenelactone isolated from the roots of Saussurealappa.
Purity: 99.97%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
www.MedChemExpress.com 23
Dehydroeburicoic acid monoacetate (3-O-Acetyldehydroeburicoic acid) Cat. No.: HY-N4125
Dehydroeburicoic acid monoacetate (Compound 18) isa lanostane triterpenoid isolated from
.Wolfiporia cocos
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg
DehydroleucodineCat. No.: HY-122295
Dehydroleucodine is a sesquiterpene lactoneisolated from . Dehydroleucodine isGynoxys verrucosaa mast cell stabilizer that inhibits tmast celldegranulation induced by compound 48/80.Dehydroleucodine inudces cells , and hasapoptosisgastric ulcer inhibition and antileukemic effects.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DemethylzeylasteralCat. No.: HY-N0587
Demethylzeylasteral is a triterpene compoundisolated from Hook F,Tripterygium wilfordiiwith anti-inflammatory, immunosuppressive andanti-tumor activities. Demethylzeylasteral cansignificantly alleviates atherosclerosis (AS).
Purity: 99.90%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
DeoxyandrographolideCat. No.: HY-N0857
Deoxyandrographolide, isolated from the, suppresses LPS inducedAndrographis paniculata
increase in mRNA levels of iNOS as well asproduction of proinflammatory mediators TNF-α andIL-6. Deoxyandrographolide potentiates NGF-inducedneurite outgrowth.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
DeoxyelephantopinCat. No.: HY-N2491
Deoxyelephantopin, a natural bioactivesesquiterpene lactone from , hasElephantopus scabershown promising anticancer effects against a broadspectrum of cancers. Deoxyelephantopin inhibits
, , , and signaling.NF-κB MAPK PI3K/Akt β-catenin
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Dihydroartemisinin (Dihydroqinghaosu; β-Dihydroartemisinin; Artenimol) Cat. No.: HY-N0176
Dihydroartemisinin is a potent anti-malariaagent.
Purity: 99.03%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg, 200 mg, 500 mg
DihydrocephalomannineCat. No.: HY-N7256
Dihydrocephalomannine (compound 1b), an analogueof Paclitaxel, shows reduced cytotoxicity andtubulin binding compared to Paclitaxel.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Dihydrocucurbitacin BCat. No.: HY-N4171
Dihydrocucurbitacin B, a triterpene isolated from roots, inhibits nuclear factor ofCayaponia tayuya
activated T cells ( ), induces cell cycleNFATarrested in the G0 phase, and inhibits delayedtype hypersensitivity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Diosbulbin BCat. No.: HY-N0429
Diosbulbin B is a diterpene lactone isolated from, with anti-tumor activity.D. bulbifera L.
Diosbulbin B can induce liver injury.
Purity: 99.90%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg
Dipotassium glycyrrhizinateCat. No.: HY-N0184A
Dipotassium glycyrrhizinate is a natural compound,inhibits atopic dermatitis-related gene expressionwith anti-anti-inflammatory activity.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
24 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Dipsacoside BCat. No.: HY-N0266
Dipsacoside B is a major bioactive saponin, whichcan be used as a marker.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 50 mg
Docetaxel (RP-56976) Cat. No.: HY-B0011
Docetaxel (RP-56976) is a inhibitor,microtubule depolymerization
with an of 0.2 μM. Docetaxel attenuates theIC50
effects of and gene expression.bcl-2 bcl-xLDocetaxel arrests the cell cycle at G2/M and leadsto cell .apoptosis
Purity: 99.96%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 200 mg
Docetaxel Trihydrate (RP-56976 Trihydrate) Cat. No.: HY-B0011A
Docetaxel Trihydrate (RP-56976 Trihydrate) is anantineoplastic agent and inhibits
with an microtubule depolymerization IC50
value of 0.2 μM. Docetaxel Trihydrate is asemisynthetic analog of taxol and attenuates the.
Purity: 99.86%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg
Dodecanoic acid ingenol esterCat. No.: HY-N0867
Dodecanoic acid ingenol ester is a naturalcompound.
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg
Dulcoside ACat. No.: HY-N6992
Dulcoside A is isolated from , itStevia rebaudianaoften advertised as a sweetener.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Echinocystic acidCat. No.: HY-N0271
Echinocystic acid a pentacyclic triterpeneisolated from the fruits of Gleditsia sinensisLam, has potent antioxidant, anti-inflammatory andanti-tumor properties. In vitro: Echinocystic acid(EA) inhibit the formation of osteoclast.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Eclalbasaponin ICat. No.: HY-N7022
Eclalbasaponin I is isolated from Eclipta prostrata with antitumor activity. Eclalbasaponin IL
inhibits the proliferation of hepatoma cellsmmc-7721 with an IC value of 111.1703 μg/ml.50
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
Ecliptasaponin ACat. No.: HY-N1508
Ecliptasaponin A , a pentacyclic triterpenoidsaponin, is one of major compounds separated from
.Eclipta prostrate
Purity: 99.05%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Ecliptasaponin DCat. No.: HY-N2191
Ecliptasaponin D is a triterpenoid glucosideisolated from (L.) Hassk which is theEclipta albaaerial part of .Eclipta prostrate
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Eleutheroside ECat. No.: HY-N0272
Eleutheroside E, a principal component ofEleutherococcus enticosus, has anti-inflammatoryand protective effects in ischemia heart.
Purity: 99.65%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
www.MedChemExpress.com 25
Emodin-8-glucosideCat. No.: HY-N0311
Emodin-8-glucoside is an anthraquinone derivativeisolated from Aloe vera, binds to minor groove ofDNA.
Purity: 98.32%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Englerin ACat. No.: HY-133168
Englerin A is a potent and selective activator of and channels, with s of 11.2TRPC4 TRPC5 EC50
and 7.6 nM, respectively. Englerin A can inducerenal carcinoma cells death by elevated Ca2+
influx and Ca cell overload.2+
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Epibetulinic acidCat. No.: HY-N0223
Epibetulinic acid, isolated from the root bark of and the leaves of Maytenus cuzcoina Maytenus
, exhibits potent inhibitory effects onchiapensis and prostaglandin E2 ( ) production inNO PGE2
mouse macrophages (RAW 264.7) stimulated withbacterial endotoxin with s of 0.7 and 0.6…IC50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
EpifriedelanolCat. No.: HY-N1931
Epifriedelanol is a triterpenoid isolated from theroot bark of , with antitumorUlmus davidianaactivity. Epifriedelanol inhibits cellularsenescence in human primary cells.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
ErgolideCat. No.: HY-N6893
Ergolide is a sesquiterpene lactone isolated fromthe dried flowers of . ErgolideInula Britannicainhibits inducible nitric oxide synthase andcyclo-oxygenase-2 expression in RAW 264.7macrophages through the inactivation of .NF-κB
Purity: 99.13%Clinical Data:Size: 5 mg, 10 mg
ErythrodiolCat. No.: HY-N2419
Erythrodiol is an olive oil component. Erythrodiolpromotes Cholesterol efflux (ChE) by selectivelyinhibiting the degradation of protein.ABCA1Erythrodiol is a good candidate to be furtherexplored for therapeutic or preventive applicationin the context of atherosclerosis.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
EscinCat. No.: HY-B2114
Escin, a natural mixture of triterpenoid saponinsisolated from horse chestnut (Aesculushippocastanum) seeds, can be used as avasoprotective anti-inflammatory, anti-edematousand anti-nociceptive agent.
Purity: >95.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg
Escin IBCat. No.: HY-N0555
Escin IB is a saponin isolated from skin and theendosperm of seeds of horse chestnut (Aesculus
). Escin IB shows inhibitoryhippocastanumeffect on activity.pancreatic lipase
Purity: 98.60%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg
Esculentoside ACat. No.: HY-N0632
Esculentoside A (EsA), a kind of triterpenesaponin isolated from roots of .Phytolacca esculentaEsculentoside A (EsA) possesses anti-inflammatoryactivity in acute and chronic experimental models,has selective inhibitory activity towardscyclooxygenase-2 ( ).COX-2
Purity: 98.27%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Esculentoside HCat. No.: HY-N2205
Esculentoside H (EsH) is a water-soluble saponinisolated and purified from the root extract ofperennial plant Phytolacca esculenta.Esculentoside H (EH) has anti-tumor activity, themechanism is related to the capacity for
release.TNF
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
26 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
EsculinCat. No.: HY-N0188
Esculin, a fluorescent coumarin glucoside, is anactive ingredient of ash bark. Esculin amelioratescognitive impairment in experimental diabeticnephropathy (DN), and exerts antioxidative stressand antiinflammatory effects, via the MAPKsignaling pathway.
Purity: 99.97%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 500 mg
Eupalinilide BCat. No.: HY-N6955
Eupalinilide B is a sesquiterpenoid isolated fromGenus .Eupatorium
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Eupalinolide BCat. No.: HY-N0753
Eupalinolide B is a germacrane sesquiterpeneisolated from .Eupatorium lindleyanumEupalinolide B demonstrates potent cytotoxicityagainst A-549, BGC-823 and HL-60 tumour celllines.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Eupalinolide KCat. No.: HY-N2240
Eupalinolide K, a sesquiterpene lactones compoundfrom , is a Eupatorium lindleyanum STAT3inhibitor. Eupalinolide K is a Michael reactionacceptor (MRA) .
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
EupholCat. No.: HY-N0313
Euphol is a tetracyclic triterpene alcoholisolated from the sap of withEuphorbia tirucallianti-mutagenic, anti-inflammatory andimmunomodulatory effects, orally active.
Purity: 98.82%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Euphorbadienol (alpha-Euphorbol) Cat. No.: HY-125648
Euphorbadienol (alpha-Euphorbol), a triterpeniccompound, isolated from the latex of Euphorbia
. The derivatives of Euphorbadienol canresiniferabe used as elicitors of disease resistance, andhas antileishmanial and antitrypanosomal activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Euphorbia Factor L1Cat. No.: HY-N2557
Euphorbia Factor L1 is a diterpenoid from Euphorbia L., reduces the expression of Bcl-2, PI3K,lathyris
AKT and mTOR protein and mRNA, upregulates cleavedcaspase-9 and caspase-3 levels, buts shows noeffect on pro-caspase-9 and pro-caspase-3.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Euphorbia Factor L2Cat. No.: HY-N5001
Euphorbia factor L2, a lathyrane diterpenoidisolated from caper euphorbia seed (the seeds of
L.), has been traditionallyEuphorbia lathyrisapplied to treat cancer. Euphorbia factor L2 showspotent cytotoxicity and induces via aapoptosismitochondrial pathway.
Purity: 99.65%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
EuphorbiasteroidCat. No.: HY-N2032
Euphorbiasteroid is a tricyclic diperpene of L., inhibits tyrosinase, andEuphorbia lathyris
increases the phosphorylation of , withAMPKanti-cancer, anti-virus, anti-obesity andmultidrug resistance-modulating effect.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Eupteleasaponin ICat. No.: HY-N5095
Eupteleasaponin I is a component of Euptelea, may has gastroprotective activity.polyandra
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
www.MedChemExpress.com 27
Euscaphic acidCat. No.: HY-N2566
Euscaphic acid, a inhibitor, isDNA polymerasea triterpene from the root of the R. alceaefolius
. Euscaphic inhibits calf DNA polymerase α (polPoirα) and rat DNA polymerase β (pol β) with IC50
values of 61 and 108 μM. Euscaphic acid induces.apoptosis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
FarnesolCat. No.: HY-Y0248A
Farnesol is a sesquiterpene alcohol that modulatescell-to-cell communication in , andCandida albicanshas the activity in inhibiting bacteria.
Purity: 99.41%Clinical Data: No Development ReportedSize: 500 mg
Farnesyl acetateCat. No.: HY-128430
Farnesyl acetate is a sesquiterpene isolated fromthe leaves of . FarnesylAmomum gagnepainiiacetate has significant toxicity against red palmweevil larvae with a LD of 7867 ppm.50
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
Fenchyl alcoholCat. No.: HY-N7107
Fenchyl alcohol is a monoterpene alcohol in theessential oils isolated from Douglas fir needles,acts as a fragrance. Fenchyl alcohol stronglyinhibits the rumen microbial activity of bothsheep and deer.
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
FeretosideCat. No.: HY-N6249
Feretoside, a phenolic compound extracted from thebarks of , is a which actE. ulmoides HSP induceras cytoprotective agent.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
FerulenolCat. No.: HY-129605
Ferulenol, a sesquiterpene prenylated coumarinderivative, specifically inhibits succinateubiquinone reductase at the level of theubiquinonecycle. Ferulenol shows goodantimycobacterial activity and haemorrhagicaction.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Formosanin CCat. No.: HY-N2389
Formosanin C is a diosgenin saponin isolated from and an immunomodulator withParis formosana Hayata
antitumor activity. Formosanin C inducesapoptosis.
Purity: 99.28%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
Forskolin (Coleonol; Colforsin) Cat. No.: HY-15371
Forskolin (Coleonol) is a potent adenylate cyclaseactivator with an of 41 nM and an ofIC50 EC50
0.5 μM for . Forskolin istype I adenylyl cyclasealso an inducer of intracellular cAMPformation.
Purity: 99.82%Clinical Data: No Development ReportedSize: 10 mg, 50 mg, 100 mg, 200 mg
FuranodienoneCat. No.: HY-N2184
Furanodienone is one of the major bioactiveconstituents derived from .Rhizoma CurcumaeFuranodienone induced .apoptosis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ganoderenic acid ACat. No.: HY-N2998
Ganoderenic acid A is a lanostane-type triterpeneisolated from . GanoderenicGanoderma lucidumacid A is a potent inhibitor of .β-glucuronidaseGanoderenic acid A has a potent hepatoprotectiveeffect against CCl4-induced liver injury.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
28 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Ganoderenic acid CCat. No.: HY-N1515
Ganoderenic acid C is a triterpenoid isolated from. Ganoderenic acid C isGanoderma lingzhi
abundant in fruit bodies at an early growth stage.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ganoderenic acid ECat. No.: HY-N6867
Ganoderenic acid E is a lanostane-type triterpeneisolated from .Ganoderma lucidum
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ganoderic acid ACat. No.: HY-N1447
Ganoderic acid A can inhibit of the JAK-STAT3signaling pathway, also inhibit proliferation,viability, ROS.
Purity: 99.84%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg, 25 mg
Ganoderic acid BCat. No.: HY-N2006
Ganoderic acid B is a triterpene isolated from amushroom . Ganoderic acid BGanoderma luciduminhibits the activation of Epstein-Barr virus(EBV) antigens as telomerase inhibitor. Ganodericacid B is a moderately active inhibitor against
.HIV-1 protease
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ganoderic acid C2Cat. No.: HY-N1517
Ganoderic acid C2 is a bioactive triterpenoid in. Ganoderic acid C2Ganoderma lucidum
possesses the potential anti-tumor bioactivity,antihistamine, anti-aging and cytotoxic effects.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ganoderic acid DCat. No.: HY-N1511
Ganoderic acid D, a highly oxygenated tetracyclictriterpenoid, is the major active component of
. Ganoderic acid DGanoderma lucidumupregulates the protein expression of andSIRT3induces the deacetylated cyclophilin D (CypD) bySIRT3.
Purity: 99.40%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ganoderic acid GCat. No.: HY-N2458
Ganoderic acid G is a triterpene isolated from thesurface part of gills of .Ganoderma lucidum
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Ganoderic acid HCat. No.: HY-N1513
Ganoderic acid H is a lanostane-type triterpeneisolated from . GanodericGanoderma lucidumacid H suppresses growth and invasive behavior ofbreast cancer cells through the inhibition oftranscription factors AP-1 and NF-kappaBsignaling.
Purity: 97.14%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ganoderic acid TRCat. No.: HY-129150
Ganoderic acid TR is a broad-spectrum inhibitoragainst ,influenza neuraminidases (NAs)particularly H5N1 and H1N1 neuraminidases. The
values of 10.9 and 4.6 μM, respectively.IC50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ganoderic acid YCat. No.: HY-125713
Ganoderic acid Y is a inhibitor withα-glucosidasean of 170 μM for yeast α-glucosidase.IC50
Ganoderic acid Y inhibits enterovirus 71 (EV71) through blocking EV71 uncoating.replication
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
www.MedChemExpress.com 29
GanodermanondiolCat. No.: HY-N2996
Ganodermanondiol is a melanogenesis inhibitorisolated from the Ganoderma
.Ganodermanondiol exhibits potentlucidumcytoprotective effects on tert-butylhydroperoxide-induced hepatotoxicity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
GanodermanontriolCat. No.: HY-N1506
Ganodermanontriol, a sterol isolated from, induces anti-inflammatoryGanoderma lucidum
activity in tert-butyl hydroperoxide(t-BHP)-damaged hepatic cells through theexpression of HO-1. Ganodermanontriol exhibitshepatoprotective activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ganolactone BCat. No.: HY-N2234
Ganolactone B is a lanostane-type triterpeneisolated from the fruiting bodies of .G. sinense
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Gardenoin JCat. No.: HY-N3930
Gardenoin J, a cycloartane triterpene, is isolatedfrom the exudate of .Gardenia thailandica
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
GardenosideCat. No.: HY-N1478
Gardenoside is a natural compound found in Gardeniafruits, with hepatoprotective properties.Gardenoside suppresses the pain of chronicconstriction injury by regulating the P2X3 andP2X7 receptors.
Purity: 99.37%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Genipin ((+)-Genipin) Cat. No.: HY-17389
Genipin ((+)-Genipin) is a natural crosslinkingreagent derived from Gardenia jasminoides Ellisfruits. Genipin inhibits UCP2 (uncoupling protein2) in cells.
Purity: 99.40%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg, 100 mg
Genipin 1-β-D-gentiobioside (Genipin 1-gentiobioside; Genipin
1-β-gentiobioside; Genipin gentiobioside) Cat. No.: HY-N2094
Genipin 1-β-D-gentiobioside (Genipin1-gentiobioside) is one of the most abundant andbioactive iridoid glycosides in Gardenia
Ellis, which possessesjasminoideshepatoprotective, anti-inflammatory, antioxidant,and antithrombotic activities.
Purity: 99.56%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg
GeniposideCat. No.: HY-N0009
Geniposide is an iridoid glucoside extracted from fruits; exhibits a varityGardenia jasminoides Ellis
of biological activities such as anti-diabetic,antioxidative, antiproliferative andneuroprotective activities.
Purity: 99.52%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg, 100 mg, 500 mg
Geniposidic acidCat. No.: HY-N0010
Geniposidic acid is an effective anticancer andradioprotection agent. Target: Others Mice weregiven an intraperitoneal injection of Geniposidicacid (GA) (12.5, 25, 50 mg/kg) 1 h beforereceiving GA against d-galactosamine (GalN) (800mg/kg)/LPS (40 μg/kg).
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Gentiopicroside (Gentiopicrin) Cat. No.: HY-N0494
Gentiopicroside, a naturally occurring iridoidglycoside, inhibits activity, with an ICP450 50
and a K of 61 µM and 22.8 µM for CYP2A6;i
Gentiopicroside has antianti-inflammatoryandantioxidative effects.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 25 mg, 50 mg, 100 mg
30 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Geoside (Gein; Eugenyl vicianoside) Cat. No.: HY-N6903
Geoside (Gein) is a natural compound isolated fromstevia rebaudiana.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
GeraniolCat. No.: HY-N6952
Geraniol, an olefinic terpene, was found toinhibit growth of andCandida albicans
strains.Saccharomyces cerevisiae
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Gibberellic acid (Gibberellin A3) Cat. No.: HY-N1964
Gibberellic Acid is named after a fungus Gibberella. Gibberellic Acid regulates processes offujikuroi
plant development and growth, including seeddevelopment and germination, stem and root growth,cell division, and flowering time.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Ginkgolide A (BN-52020) Cat. No.: HY-B0355
Ginkgolide A (BN-52020) is an extract from inGinkgo biloba and a g-aminobutyric acid (GABA)antagonist.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Ginkgolide B (BN-52021) Cat. No.: HY-N0784
Ginkgolide B (BN-52021), an important activeterpenoid from Ginkgo biloba leaves, is reportedto increase cell viability and decrease cellapoptosis.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Ginkgolide C (BN-52022; Ginkgolide-C) Cat. No.: HY-N0785
Ginkgolide C is a flavone isolated from Ginkgo leaves, possessing multiple biologicalbiloba
functions, such as decreasing platelet aggregationand ameliorating Alzheimer disease.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Ginkgolide JCat. No.: HY-N0786
Ginkgolide J is a main constituent of thenon-flavone fraction of with an Ginkgo biloba IC50
range of 12-54 µM, has neuroprotective and antineuronal apoptotic ability.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Ginkgolide KCat. No.: HY-N4176
Ginkgolide K, isolated from , inducesGinkgo bilobaprotective autophagy through the AMPK/mTOR/ULK1signaling pathway. Ginkgolide K possessesneuroprotective activity.
Purity: 99.83%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg, 25 mg
Ginsenoside C-K (Ginsenoside compound K; Ginsenoside K) Cat. No.: HY-N0904
Ginsenoside C-K, a bacterial metabolite of G-Rb1,exhibits anti-inflammatory effects by reducing iNOSand . Ginsenoside C-K exhibits an inhibitionCOX-2against the activity of and inCYP2C9 CYP2A6human liver microsomes with s of 32.0±3.6 μMIC50
and 63.6±4.2 μM, respectively.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside F1 (20(S)-Ginsenoside F1) Cat. No.: HY-N0598
Ginsenoside F1, an enzymatically modifiedderivative of Ginsenoside Rg1, demonstratescompetitive inhibition of activity andCYP3A4weaker inhibition of CYP2D6 activity.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
www.MedChemExpress.com 31
Ginsenoside F2Cat. No.: HY-125848
Ginsenoside F2, a metabolite from Ginsenoside Rb1,induces apoptosis accompanied by protectiveautophagy in breast cancer stem cells.
Purity: 99.95%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
Ginsenoside F3Cat. No.: HY-N0600
Ginsenoside F3, a component of PPTGs (an minorsaponin in the leaves of ), hasPanax ginsengimmunoenhancing activity by regulating productionand gene expression of type 1 cytokines (IL-2,IFN-gamma) and type 2 cytokines (IL-4 and IL-10).
Purity: 99.84%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg
Ginsenoside F4Cat. No.: HY-N2503
Ginsenoside F4 (GF4), ginseng saponinis, isolatedfrom notoginseng or red ginseng. Ginsenoside F4(GF4) has inhibitory effect on human lymphocytomaJK cell by inducing its .apoptosis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ginsenoside Ra1Cat. No.: HY-N2506
Ginsenoside Ra1 is a component from ginseng,inhibits protein tyrosine kinase ( ) activationPTKinduced by hypoxia/reoxygenation.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ginsenoside Ra2Cat. No.: HY-N4260
Ginsenoside Ra2 is a component from .Panax ginseng
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ginsenoside Ra3Cat. No.: HY-N4259
Ginsenoside Ra3, isolated from ,Panax ginsengpossesses anti-cancer activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ginsenoside Rb1 (Gypenoside III) Cat. No.: HY-N0039
Ginsenoside Rb1, a main constituent of the root ofPanax ginseng, inhibits Na , K -ATPase+ +
activity with an of 6.3±1.0 μM. GinsenosideIC50
also inhibits activation and phosphorylationIRAK-1of .NF-κB p65
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
Ginsenoside Rb2 (Ginsenoside C) Cat. No.: HY-N0040
Ginsenoside Rb2 is one of the main bioactivecomponents of ginseng extracts. Rb2 can upregulate
gene expression. Ginsenoside Rb2 hasGPR120antiviral effects.
Purity: 98.26%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside Rb3 (Gypenoside IV) Cat. No.: HY-N0041
Ginsenoside Rb3 is extracted from steamed Panax. Ginsenoside Rb3 exhibits inhibitorynotoginseng
effect on TNFα-induced transcriptionalNF-κBactivity with an of 8.2 μM in 293T cellIC50
lines. Ginsenoside Rb3 also inhibits the inductionof and mRNA.COX-2 iNOS
Purity: 99.12%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside Rc (Panaxoside Rc) Cat. No.: HY-N0042
Ginsenoside Rc, one of major Ginsenosides from, enhances GABA receptorPanax ginseng A
( )-mediated ion channel currents (I ).GABAA GABA
Ginsenoside Rc inhibits the expression of TNF-αand .IL-1β
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
32 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Ginsenoside Rd (Gypenoside VIII) Cat. No.: HY-N0043
Ginsenoside Rd inhibits TNFα-induced NF-κBtranscriptional activity with an ofIC50
12.05±0.82 μM in HepG2 cells. Ginsenoside Rdinhibits expression of and mRNA.COX-2 iNOSGinsenoside Rd also inhibits influx.Ca2+
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside Rf (Panaxoside Rf) Cat. No.: HY-N0601
Ginsenoside Rf is a trace component of ginsengroot. Ginsenoside Rf inhibits N-type Ca2+
.channel
Purity: >95.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside Rg1 (Panaxoside A; Panaxoside Rg1) Cat. No.: HY-N0045
Ginsenoside Rg1 is one of the major activecomponents of ginseng. Ginsenoside Rg1 displayspromising effects by reducing cerebral levels.AβGinsenoside Rg1 also reduces nuclearNF-κBtranslocation.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside Rg2 (Chikusetsusaponin I; Panaxoside Rg2; Prosapogenin C2) Cat. No.: HY-N0602
Ginsenoside Rg2 is one of the major activecomponents of ginseng. Ginsenoside Rg2 acts as a
inhibitor. Ginsenoside Rg2 also reducesNF-κB accumulation.Aβ1-42
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside Rg5Cat. No.: HY-N0908
Ginsenoside Rg5 is the main component of Redginseng. Ginsenoside blocks binding of to itsIGF-1receptor with an of ~90 nM. Ginsenoside Rg5IC50
also inhibits the mRNA expression of viaCOX-2suppression of the DNA binding activities of
.NF-κB p65
Purity: 99.86%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside Rg6Cat. No.: HY-N0907
Ginsenoside Rg6 is the component isolated fromnotoginseng. Ginsenoside Rg6 inhibitsTNF-α-induced transcriptional activity withNF-κBan of 29.34±2.22 μM in HepG2 cells.IC50
Ginsenoside Rg6 also exhibits -inducingapoptosiseffect.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ginsenoside Rh1 (Prosapogenin A2; Sanchinoside B2; Sanchinoside Rh1) Cat. No.: HY-N0604
Ginsenoside Rh1 (Prosapogenin A2; Sanchinoside B2;Sanchinoside Rh1) is isolated from the root of
. Ginsenoside Rh1 inhibits thePanax Ginsengexpression of , , , and .PPAR-γ TNF-α IL-6 IL-1β
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside Rh2 (20(S)-Ginsenoside Rh2; 20(S)-Rh2; Ginsenoside-Rh2) Cat. No.: HY-N0605
Ginsenoside Rh2 is isolated from the root of. Ginsenoside Rh2 induces the activation ofGinseng
and . Ginsenoside Rh2 inducescaspase-8 caspase-9cancer cell in a multi-path manner.apoptosis
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Ginsenoside Rh3Cat. No.: HY-N0606
Ginsenoside Rh3 is a bacterial metabolite ofGinsenoside Rg5. Ginsenoside Rh3 treatment inhuman retinal cells induces activation.Nrf2
Purity: 99.95%Clinical Data: No Development ReportedSize: 5 mg
Ginsenoside Rh7Cat. No.: HY-N4262
Ginsenoside Rh7 is a minor saponin isolated fromthe leaves of .Panax ginseng
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
www.MedChemExpress.com 33
Ginsenoside Rk1Cat. No.: HY-N2515
Ginsenoside Rk1 is a unique component created byprocessing the ginseng plant (mainly Sung Ginseng,SG) at high temperatures. Ginsenoside Rk1 hasanti-inflammatory effect, suppresses theactivation of signaling pathway andJak2/Stat3
.NF-κB
Purity: 98.53%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Ginsenoside Rk2Cat. No.: HY-N2504
Ginsenoside Rk2 is a dammarane glycoside isolatedfrom the processed ginseng (SG; Sun Ginseng).
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ginsenoside Rk3Cat. No.: HY-N0906
Ginsenoside Rk3 is present in the roots Panax herbs. Ginsenoside Rk3 significantlynotoginseng
inhibits TNF-α-induced transcriptionalNF-κBactivity, with an of 14.24±1.30 μM in HepG2IC50
cells.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 25 mg
Ginsenoside Ro (Polysciasaponin P3; Chikusetsusaponin 5;
Chikusetsusaponin V) Cat. No.: HY-N0607
Ginsenoside Ro (Polysciasaponin P3;Chikusetsusaponin 5; Chikusetsusaponin V) exhibitsa -antagonistic antiplatelet effect with anCa2+
IC of 155 μM. Ginsenoside Ro reduces the50
production of more than it reduces theTXA2
activities of COX-1 and TXAS.
Purity: 99.21%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Glaucocalyxin ACat. No.: HY-N2112
Glaucocalyxin A, an ent-kauranoid diterpene from var., induces apoptosis inRabdosia japonica
osteosarcoma by inhibiting nuclear translocationof Five-zinc finger Glis 1 (GLI1) via regulating
signaling pathway. Glaucocalyxin A hasPI3K/Aktantitumor effect.
Purity: 99.38%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Glycochenodeoxycholic acid sodium salt(Chenodeoxycholylglycine sodium salt; …) Cat. No.: HY-N2334A
Glycochenodeoxycholic acid sodium salt(Chenodeoxycholylglycine sodium salt) is a bileacid formed in the liver from chenodeoxycholateand glycine. It acts as a detergent to solubilizefats for absorption and is itself absorbed.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Glycyrrhizic acid (Glycyrrhizin) Cat. No.: HY-N0184
Glycyrrhizic acid is a triterpenoid saponinl,acting as a direct antagonist, withHMGB1anti-tumor, anti-diabetic activities.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg, 200 mg
GracillinCat. No.: HY-N0706
Gracillin is a kind of steroidal saponin isolatedfrom the root bark of wild yam Dioscorea nipponicawith antitumor agent. Gracillin could induce cellcycle arrest, oxidative stress, and apoptosis inHL60 cells.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg
GuaiazuleneCat. No.: HY-N6951
Guaiazulene is present in several essential oilsof medicinal and aromatic plants, with antioxidantactivity. Guaiazulene has in vitro cytotoxicactivity against neuron and N2a neuroblastom(N2a-NB) cells.
Purity: >98.0%Clinical Data: LaunchedSize: 5 mg
Guggulsterone (Z/E-Guggulsterone) Cat. No.: HY-107738
Guggulsterone is a plant sterol derived from thegum resin of the tree .Commiphora wightii
Purity: 99.50%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
34 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
GymnemageninCat. No.: HY-N2268
Gymnemagenin is a triterpenoid isolated from G.. Gymnemagenin is an agent for diabetessylvestre
and obesity and also possesses antiviralproperties.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Gymnemic acid ICat. No.: HY-N2541
Gymnemic acid I is a bioactive triterpene saponinfound in . Gymnemic acid IGymnema sylvestredecreases the apoptosis under the high glucosestress.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
GymnestrogeninCat. No.: HY-N2273
Gymnestrogenin is a pentahydroxytriterpene fromthe leaves of R.Br.Gymnema sylvestreGymnestrogenin is a antagonist with s ofLXR IC50
2.5 and 1.4 μM for LXRα and LXRβ transactivation,respectively.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Gynostemma Extract (Ginsenoside C-Mx1; Gynosaponin I; Gypenoside IX) Cat. No.: HY-N0167
Gynostemma Extract (Ginsenoside C-Mx1) is anatural product.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Gypenoside ACat. No.: HY-N2440
Gypenoside A is a natural compound isolaated from.Gynostemma pentaphyllum Makino
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Gypenoside XLVICat. No.: HY-N6252
Gypenoside XLVI is one of the major dammarane-typetriterpenoid saponins from Gynostamma
. Gypenoside XLVI has a tetracyclicpentaphallumtriterpene structure and possess potent non-smallcell lung carcinoma A549 cell inhibitory activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Gypsogenin-3-O-glucuronideCat. No.: HY-N1439
Gypsogenin-3-O-glucuronide is a ubiquitous saponinprecursor in plants of the genus Gypsophila.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
HandelinCat. No.: HY-N2083
Handelin is a guaianolide dimer from that has potentChrysanthemum boreale
anti-inflammatory activity by down-regulating signaling and pro-inflammatory cytokineNF-κB
production.
Purity: 99.44%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
HarpagideCat. No.: HY-N0397
Harpagide is a class of iridoid glycoside isolatedfrom and has antiparasiticScrophularia cryptophilaactivity, which exhibits good in vitrotrypanocidal activities against African
( ) with an oftrypanosomes T.b. rhodesiense IC50
21 μg/mL.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
HarpagosideCat. No.: HY-N0396
Harpagoside is isolated from Harpagophytum. Harpagoside has inhibitory effectsprocumbens (Hp)
on and activity and inhibits NOCOX-1 COX-2production.
Purity: 98.35%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
www.MedChemExpress.com 35
HastatosideCat. No.: HY-N2015
Hastatoside is an iridoid glycoside that isisolated from and has a role inVerbena officinalispromoting sleep.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Hederacolchiside A1Cat. No.: HY-N6950
Hederacolchiside A1, isolated from Pulsatilla, suppresses proliferation of tumor cellschinensis
by inducing apoptosis through modulating signaling pathway.PI3K/Akt/mTOR
Purity: >99.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Hederacoside C (Kalopanaxsaponin B) Cat. No.: HY-N0253
Hederacoside C is a principal active ingredient ofHedera helix leaf that can treat respiratorydisorders, because of its expectorant,bronchodilator, antibacterial, andbronchospasmolytic effects.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 25 mg, 50 mg
Hederacoside DCat. No.: HY-N0254
Hederacoside D is one of the bioactive saponinsfrom , and plays pivotal roles in theHedera helixoverall biological activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
HederageninCat. No.: HY-N0256
Hederagenin is a triterpenoid saponin. It caninhibit LPS-stimulated expression of iNOS, COX-2,and NF-κB.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Hederagenin 28-O-beta-D-glucopyranosyl esterCat. No.: HY-N2190
Hederagenin 28-O-beta-D-glucopyranosyl ester, atriterpenoid saponin isolated from ,Ilex cornutaexhibits protective effects against H O -induced2 2
myocardial cell injury.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Hederasaponin BCat. No.: HY-N0306
Hederasaponin B, isolated from , hasHedera helixbroad-spectrum activity against variousantiviralsubgenotypes of Enterovirus 71 (EV71).
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Hinokitiol (β-Thujaplicin) Cat. No.: HY-B2230
Hinokitiol is a component of essential oilsisolated from , reduces Chymacyparis obtusa Nrf2expression, and decreases and UHRF1 mRNADNMT1and protein expression, with anti-infective,anti-oxidative, and anti-tumor activities.
Purity: 99.28%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg, 100 mg
Hopane-3β,22-diolCat. No.: HY-N4034
Hopane-3β,22-diol (compound 74) is a hopaneisolated from .A. mariesii
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Hosenkoside CCat. No.: HY-N2251
Hosenkoside C is a baccharane glycoside isolatedfrom the seeds of .Impatiens balsamina
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
36 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Hosenkoside GCat. No.: HY-N2242
Hosenkoside G, a baccharane glycoside isolatedfrom the seeds of L.,Impatiens Balsaminapossesses anti-tumor activity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Icariside B1Cat. No.: HY-N8083
Icariside B1 is a megastigmane glycoside compoundisolated from Franch, with anPetasites tricholobusanticancer effect.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ilexhainanoside DCat. No.: HY-N5040
Ilexhainanoside D is the main triterpenoid saponinextracted from Merr., and theIlex hainanensiscombination of Ilexhainanoside D and ilexsaponinA1 has anti-inflammation effect.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ilexsaponin ACat. No.: HY-N2638
Ilexsaponin A, isolated from the root of Ilexpubescens, attenuates ischemia-reperfusion-inducedmyocardial injury through pathway.anti-apoptotic
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Ilexsaponin B2Cat. No.: HY-N6256
Ilexsaponin B2 is a saponin isolated from the rootof Hook. et Arn. Ilexsaponin B2 is aIlex pubescenspotent and phosphodiesterase 5 (PDE5) PDEIinhibitor with values of 48.8 μM and 477.5IC50
μM, respectively.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
IncensoleCat. No.: HY-N4097
Incensole, a 14-membered diterpenoid, is isolatedfrom both essential oils and resins offrankincense. Incensole has shownanti-inflammatory and anti-depression activitiesdue to their ability to activate ion channels inthe brain to alleviate anxiety or depression.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 25 mg, 50 mg
Ingenol ((-)-Ingenol) Cat. No.: HY-N0865
Ingenol is a activator, with a of 30 μM,PKC Ki
with antitumor activity.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
Ingenol Mebutate (Ingenol 3-angelate; PEP005) Cat. No.: HY-B0719
Ingenol Mebutate is an active ingredient in, acts as a potent modulator,Euphorbia peplus PKC
with s of 0.3, 0.105, 0.162, 0.376, and 0.171 nMKi
for PKC-α, PKC-β, PKC-γ, PKC-δ, and PKC-ε,respectively, and has antiinflammatory andantitumor activity.
Purity: 99.07%Clinical Data: LaunchedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
Ingenol-3,4,5,20-diacetonide (Ingenol 3,4:5,20-bisacetonide) Cat. No.: HY-N0871
Ingenol-3,4,5,20-diacetonide is a naturalcompound.
Purity: 98.60%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg
Ingenol-5,20-acetonideCat. No.: HY-N0869
Ingenol-5,20-acetonide is an intermediate fromingenol for synthesis of ingenoids; improvedstability compared to ingenol.
Purity: 99.73%Clinical Data: No Development ReportedSize: 1 mg
www.MedChemExpress.com 37
Ingenol-5,20-acetonide-3-O-angelate (Ingenol 5,20-acetonide
3-angelate; Ingenol 3-angelate 5,20-acetonide) Cat. No.: HY-N0870
Ingenol-5,20-acetonide-3-O-angelate is a naturalcompound.
Purity: 98.18%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg
Inulicin (1-O-Acetylbritannilactone) Cat. No.: HY-N0896
Inulicin (1-O-Acetylbritannilactone) is an activecompound isolated from . InulicinInula Britannica L(1-O-Acetylbritannilactone) inhibits VEGF-mediatedactivation of and .Src FAK
Purity: 99.42%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
IpecosideCat. No.: HY-N2261
Ipecoside is an alkaloid isolated from .Psychotria
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Isoalantolactone ((+)-Isoalantolactone; Isohelenin) Cat. No.: HY-N0780
Isoalantolactone is an inducer, whichapoptosisalso acts as an alkylating agent.
Purity: 99.99%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Isoastragaloside I (Isoastragaloside-I) Cat. No.: HY-N0887
Isoastragaloside I is a natural compound from themedicinal herb Radix Astragali; possesses theactivity of elevating adiponectin production.
Purity: 99.43%Clinical Data: No Development ReportedSize: 1 mg
Isoastragaloside II (Astrasieversianin-VII) Cat. No.: HY-N0888
Isoastragaloside II is an astragaloside, which isisolated from the hairy root culture of Astragalusmembranaceus.
Purity: 99.38%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
Isoastragaloside IVCat. No.: HY-N4214
Isoastragaloside IV is a triterpene oligoglycosideisolated from .Astragali Radix
Purity: >99.0%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
IsocolumbinCat. No.: HY-N3050
Isocolumbin is a diterpenoid isolated from Miers (Colombo root).Jateorhiza palmate
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
IsodeoxyelephantopinCat. No.: HY-N2585
Isodeoxyelephantopin is a sesquiterpene lactoneisolated from Elephantopus scaber.Isodeoxyelephantopin induces ROS generation,suppresses NF-κB activation. Isodeoxyelephantopinalso modulates LncRNA expression and exhibitactivities against breast cancer.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Isoescin IACat. No.: HY-N0556
Isoescin IA is a triterpenoid saponin isolatedfrom the seeds of . Isoescin IAAesculus chinensishas activity.anti-HIV-1 protease
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg
38 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Isoescin IBCat. No.: HY-N0557
Isoescin IB, isolated from horse chestnut treeseeds, is an isomer of Escin IB. Isoescin IB andEscin IB are the chief active ingredients inescin.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg
Isoforskolin (Coleonol B) Cat. No.: HY-N6927
Isoforskolin is the principle active component of native to China. Isoforskolin reducesC. forskohlii
the secretion of lipopolysaccharide (LPS)-inducedcytokines, namely , , and , inTNF-α IL-1β IL-6 IL-8human mononuclear leukocytes.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Isolimonexic acidCat. No.: HY-N8405
Isolimonexic acid is a limonoid isolated fromlemon ( ) seed, hasCitrus lemon L. Burmanti-cancer and (anti-aromatase IC =25.6050
) properties.μM
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
IsorosmanolCat. No.: HY-N4191
Isorosmanol is an abietane-type diterpene isolatedfrom the leaves of sage, with antioxidant,neuroprotective and neurotrophic effects.Isorosmanol inhibits activity and melaninAChEsynthesis.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
IsoscabertopinCat. No.: HY-N2596
Isoscabertopin is a sesquiterpene lactone isolatedfrom and shows Elephantopus scaber L anti-tumoractivities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Isosteviol ((-)-Isosteviol; iso-Steviol) Cat. No.: HY-N0872
Isosteviol ((-)-Isosteviol) is a derivative ofStevioside through acid catalyzed hydrolysis ofStevioside. Isosteviol inhibits DNA polymerase andDNA topoisomerase and has antibacterial,anticancer and anti-tuberculosis effects.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Jolkinolide BCat. No.: HY-N0732
Jolkinolide B, a bioactive diterpene isolated fromthe roots of , is knownEuphorbia fischeriana Steudto induce in cancer cells.apoptosis
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Jujuboside BCat. No.: HY-N0660
Jujuboside B is one of the major bioactiveconstituents isolated from .Zizyphus jujubaJujuboside B can inhibit platelet aggregation.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Kaji-ichigoside F1Cat. No.: HY-N2297
Kaji-ichigoside F1 is isolated from withS. cuneatahemolytic and in vitro antiviral activity.
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg
Kalii Dehydrographolidi Succinas (Potassium dehydroandrographolide succinate) Cat. No.: HY-N0677A
Kalii Dehydrographolidi Succinas (Potassiumdehydroandrographolide succinate), extracted fromherbal medicine (Burm f)Andrographis paniculataNees, is widely used for the treatment of viralpneumonia and viral upper respiratory tractinfections because of its…
Purity: 98.70%Clinical Data: LaunchedSize: 5 mg, 10 mg, 20 mg
www.MedChemExpress.com 39
KauniolideCat. No.: HY-N0843
Kauniolide(81066-45-7) is a natural compound.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Kauran-16,17-diol (ent-Kauran-16β,17-diol) Cat. No.: HY-N7422
Kauran-16,17-diol (ent-Kauran-16β,17-diol), anatural diterpene, posseses anti-tumor andinducing-apoptosis activity, with a of 17 μMIC50
on inhibiting NO production in LPS-stimulated RAW264.7 macrophages.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg
Kaurenoic acidCat. No.: HY-N1469
Kaurenoic acid is a diterpene from Sphagneticola, inhibits Inflammatory Pain by thetrilobata
inhibition of cytokine production and activationof the NO–cyclic GMP–PKG–ATP-sensitive potassiumchannel signaling pathway.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
KinsenosideCat. No.: HY-N2292
Kinsenoside is a main active component isolatedfrom plants of the genus , andAnoectochilusexhibits many biological activities andpharmacological effects.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Kongensin ACat. No.: HY-N3417
Kongensin A is a natural product isolated from. Kongensin A is an effective,Croton kongensis
covalent inhibitor that blocksHSP90-dependent necroptosishas. Kongensin A is aRIP3
potent inhibitor and an necroptosis apoptosisinducer.
Purity: >98.0%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Lasalocid (Lasalocid-A; Ionophore X-537A; Antibiotic X-537A) Cat. No.: HY-B1071
Lasalocid (Lasalocid-A; Ionophore X-537A;Antibiotic X-537A) is an antibacterial agent and acoccidiostat, used in the feed additives.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
Lasalocid sodium (Lasalocid-A sodium; Ionophore X-537A
sodium; Antibiotic X-537A sodium) Cat. No.: HY-B1071A
Lasalocid sodium (Lasalocid-A sodium) treatmentled to an increase in cell wall thickness, whilstthe quantity and sugar composition of the cellwall remained unchanged in BY-2 cells.
Purity: 97.17%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
LathyrolCat. No.: HY-N0561
Lathyrol is a natural product, and is used forcancer treatment.
Purity: 98.19%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
Leelamine hydrochlorideCat. No.: HY-110028
Leelamine hydrochloride is a tricyclic diterpenemolecule that is extracted from the bark of pinetrees.
Purity: >98%Clinical Data:Size: 1 mg, 5 mg
Levomenol ((-)-α-Bisabolol) Cat. No.: HY-N6967
Levomenol is a monocyclic sesquiterpene alcoholfound in various plants and mainly in
, which exertsMatricaria chamomillaantioxidant, anti-inflammatory, and anti-apoptoticactivities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
40 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Levopimaric acidCat. No.: HY-N7431
Levopimaric acid is a type of diterpene resin acidproduced by plants. Levopimaric acid inducescancer cell and has anticancer,apoptosisantioxidant, antibacterial and cardiovascularactivities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Licoricesaponin G2Cat. No.: HY-N6983
Licoricesaponin G2 is a pentacyclic triterpenoidisolated from .Glycyrrhiza aspera
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Limonin (Limonoic acid 3,19:16,17 dilactone) Cat. No.: HY-17411
Limonin is a triterpenoid enriched in citrusfruits, which has antivirus and antitumor ability.IC50 Value: Target: HIV; anticancer Limonin is atriterpenoid aglycone that is a bitter principleof citrus fruits.
Purity: 99.78%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg, 100 mg
LinaloolCat. No.: HY-N0368
Linalool is natural monoterpene in essential olisof coriander, acts as a competitive antagonist of
, withNmethyl d-aspartate (NMDA) receptoranti-tumor, anti-cardiotoxicity activity.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
LindenenolCat. No.: HY-N2061
Lindenenol is isolated from , withRadix linderaeantioxidant and antibacterial activities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
LinderalactoneCat. No.: HY-N0781
Linderalactone is an important sesquiterpenelactone isolated from . LinderalactoneRadix linderaeinhibits cancer growth by modulating theexpression of -related proteins andapoptosisinhibition of JAK/STAT signalling pathway.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
LinderaneCat. No.: HY-N0688
Linderane, isolated from the root of Lindera, is an irreversible inhibitorstrychnifolia
. Linderane hascytochrome P450 2C9 (CYP2C9)the potential to relieve pain and cramp.
Purity: >95.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Liquidambaric lactoneCat. No.: HY-N0497
Liquidambaric lactone is a compound isolated from Wall.Euonymus grandiflorus
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Liriope muscari baily saponins CCat. No.: HY-N0345
Liriope muscari baily saponins C is one of majoractive compounds of .L. muscari (Decne.) BailyLiriope muscari baily saponins C possesses stronganti-inflammatory, immunopharmacological andcardioprotective activities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Loganic acidCat. No.: HY-N0513
Loganic acid is an iridoid isolated from corneliancherry fruits. Loganic acid can modulatediet-induced atherosclerosis and redox status.Loganic acid has strong free radical scavengingactivity and remarkable cyto-protective effectagainst heavy metal mediated toxicity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 25 mg
www.MedChemExpress.com 41
Loganin (Loganoside) Cat. No.: HY-N0512
Loganin, a major iridoid glycoside obtained fromCorni fructus, has been shown to haveanti-inflammatory and anti-shock effects. Loganinexhibits an anti-inflammatory effect in cases ofAP and its pulmonary complications throughinhibition of NF-κB activation.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
Lucidenic acid BCat. No.: HY-N6861
Lucidenic acid B is a natural compound isolatedfrom , induces ofGanoderma lucidum apoptosiscancer cells, and causes the activation ofcaspase-9 and caspase-3, and cleavage of PARP.Lucidenic acid B does not affect the cell cycleprofile, or the number of necrotic cells.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Lucidenic acid CCat. No.: HY-N6860
Lucidenic acid C is a natural compound isolatedfrom , inhibits PMA-inducedGanoderma lucidum
activity, with anti-invasive effect onMMP-9hepatoma cells.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Lucidenic acid ECat. No.: HY-107265
Lucidenic acid E is a terpenoid from Ganoderma.lucidum
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Lucidenic acid LM1Cat. No.: HY-N6859
Lucidenic acid LM1 is a natural triterpenoidisolated from .Ganoderma lucidum
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Lucideric acid ACat. No.: HY-N6862
Lucideric acid A is a natural compound isolatedfrom , inhibits PMA-inducedGanoderma lucidum
activity, with anti-invasive effect onMMP-9hepatoma cells.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Lup-20(29)-en-28-oic acidCat. No.: HY-N6049
Lup-20(29)-en-28-oic acid, a triterpenoid saponinsof Root, possessesPulsatilla koreanaanti-inflammatory and anti-tumor effect.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
LupenoneCat. No.: HY-N2590
Lupenone, isolated from ,Rhizoma Musaebelongs to lupane type triterpenoids. Lupenoneshows various pharmacological activities includinganti-inflammatory, anti-virus, anti-diabetes,anti-cancer, improving Chagas disease withoutmajor toxicity.
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg
Lupeol (Clerodol; Monogynol B; Fagarasterol) Cat. No.: HY-N0790
Lupeol (Clerodol; Monogynol B; Fagarasterol) is anactive pentacyclic triterpenoid, hasanti-oxidant, anti-mutagenic, anti-tumor andanti-inflammatory activity.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mg, 25 mg, 50 mg, 100 mg
Macranthoidin ACat. No.: HY-N2109
Macranthoidin A is an orally active saponin from. Macranthoidin A possess protectionFlos Lonicerae
effects on hepatic injury caused by Acetaminophen,Cd, and CCl4, and conspicuous depressant effectson swelling of ear croton oil.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
42 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Macranthoidin B (Macranthoiside I) Cat. No.: HY-N0864
Macranthoidin B is a major bioactive saponin inrat plasma after oral administration of extractionof saponins from Flos Lonicerae.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Macranthoside BCat. No.: HY-N5008
Macranthoside B, isolated from Flos Lonicerae,possesses anti-bacterial activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Madecassic acidCat. No.: HY-N0569
Madecassic acid is isolated from Centella asiatica(Umbelliferae). Madecassic acid hasanti-inflammatory properties caused by ,iNOS
, , , and inhibition viaCOX-2 TNF-alpha IL-1beta IL-6the downregulation of activation in RAWNF-κB264.7 macrophage cells.
Purity: 98.34%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Madecassoside (Asiaticoside A) Cat. No.: HY-N0568
Madecassoside is a pentacyclic triterpene isolatedfrom Centella asitica (L.), as ananti-inflammatory, anti-oxidative activities andanti-aging agent.
Purity: 99.86%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg, 200 mg
Maoecrystal ACat. No.: HY-N2017
Maoecrystal A is a compound isolated from leavesof .Isodon eriocalyx
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Maslinic acid (Crategolic acid; 2α-Hydroxyoleanolic acid) Cat. No.: HY-N0629
Maslinic acid can inhibit the DNA-binding activityof and abolish the phosphorylation ofNF-κB p65
, which is required for p65 activation.IκB-α
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg
Medicagenic acid (Castanogenin) Cat. No.: HY-N2472
Medicagenic acid (Castanogenin) is isolated fromthe roots of , exhibits potentHerniaria glabra Lfungistatic effects against several plantpathogens and human dermatophytes.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
MelittosideCat. No.: HY-N0915
Melittoside is a natural compound.
Purity: 99.01%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg
MenisdaurinCat. No.: HY-N1927
Menisdaurin is a cyanogenetic glucoside isolatedfrom Flueggea virosa.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Methyl carnosateCat. No.: HY-136150
Methyl camosate is a diterpene isolated from Salvia or . Methylofficinalis Rosmarinus officinalis
camosate has potent antioxidant and anti-bacterialactivity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
www.MedChemExpress.com 43
Methyl deacetylasperulosidate (6α-Hydroxygeniposide;
Deacetylasperulosidic acid methyl ester) Cat. No.: HY-N1503
Methyl deacetylasperulosidate is an iridoidisolated from species.Borreria and Spermacoce
Purity: 99.26%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg
Methyl protogracillin (NSC-698793) Cat. No.: HY-N4277
Methyl protogracillin (NSC-698793), isolated fromthe roots of Thunb, exhibitsDioscorea oppositestrong anti-cancer activity.
Purity: >99.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
MicheliolideCat. No.: HY-N0847
Micheliolide could effectively attenuate the highglucose-stimulated activation of NF-κB, thedegradation of IκBα, and the expression of MCP-1,TGF-β1 and FN in rat mesangial cells (MCs).
Purity: 99.59%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Microhelenin CCat. No.: HY-N7595
Microhelenin C is a sesquiterpene lactone isolatedfrom , with antitumorHelenium microcephalumactivity.
Purity: >95.0%Clinical Data: No Development ReportedSize: 1 mg
MogrolCat. No.: HY-N2312
Mogrol is a biometabolite of mogrosides, and actsvia inhibition of the and pathways,ERK1/2 STAT3or reducing activation and activatingCREB
signaling.AMPK
Purity: 98.06%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg, 25 mg
Mogroside I A1Cat. No.: HY-N6854
Mogroside I A1, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: 99.77%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Mogroside I E1Cat. No.: HY-N6853
Mogroside I E1, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: 98.08%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Mogroside II-A2Cat. No.: HY-108272
Mogroside II-A2, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Mogroside II-ACat. No.: HY-N6915
Mogroside II-A is a natural product isolated from.Siraitia grosvenorii
Purity: 99.54%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Mogroside IIA1Cat. No.: HY-N6855
Mogroside IIA1, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: 99.83%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
44 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Mogroside IIeCat. No.: HY-N6814
Mogroside IIe, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Mogroside IIICat. No.: HY-N0500
Mogroside III, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Mogroside III-A1Cat. No.: HY-108271
Mogroside III-A1, a triterpenoid glycosideisolated from the extracts of Luo Han Guo, is anonsugar sweetener. Mogrosides are sweeter thansucrose. Mogrosides exhibit antioxidant,antidiabetic and anticancer activities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Mogroside III-ECat. No.: HY-N6928
Mogroside III-E is a cucurbitane-type compoundisolated from , inhibits NOSiraitia grosvenoriirelease, with anti-fibrotic activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Mogroside IVCat. No.: HY-N6945
Mogroside IV, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Mogroside IV-ACat. No.: HY-N6942
Mogroside IV-A, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Mogroside IV-ECat. No.: HY-N2456
Mogroside IV-E, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Mogroside VCat. No.: HY-N0502
Mogroside V, a triterpenoid glycoside isolatedfrom the extracts of Luo Han Guo, is a nonsugarsweetener. Mogroside V is nearly 300 times sweeterthan sucrose. Mogrosides exhibit antioxidant,antidiabetic and anticancer activities. Mogrosidesare sweeter than sucrose.
Purity: 98.10%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
Mogroside VICat. No.: HY-108275
Mogroside VI, a triterpenoid glycoside isolatedfrom the extracts of , is a nonsugarLuo Han Guosweetener. Mogrosides are sweeter than sucrose.Mogrosides exhibit antioxidant, antidiabetic andanticancer activities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Mogroside VI ACat. No.: HY-N7438
Mogroside VI A, an isomer of Mogroside VI isolatedfrom , exerts sweetness property.Luo Han GuoMogroside VI A can be used for sweetener and/ortaste modifier research.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
www.MedChemExpress.com 45
Mogroside VI BCat. No.: HY-N7439
Mogroside VI B, a cucurbitane glucoside, separatedfrom the crude extract of .Siraitia grosvenoriiMogroside VI B shows effect on activating PGC-1αtranscription.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Momordicoside ACat. No.: HY-N2111
Momordicoside A is isolated from Momordica. Momordicoside A has the inhibitorycharantia L
effect on .protein tyrosine phosphatase (PTP1B)
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Momordin IcCat. No.: HY-N0330
Momordin Ic is a principal saponin constituent of, with with anti-cancer bioactivity.Fructus Kochiae
Momordin Ic induces apoptosis through oxidativestress-regulated mitochondrial dysfunction.
Purity: 98.67%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Monoammonium glycyrrhizinate hydrateCat. No.: HY-76225
Monoammonium glycyrrhizinate hydrate has variouspharmacological actions such as anti-inflammatory,antiallergic, antigastriculcer, and antihepatitisactivities.
Purity: 97.05%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 500 mg, 1 g
Monomelittoside (Danmelittoside) Cat. No.: HY-N0916
Monomelittoside is a natural compound.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
MonotropeinCat. No.: HY-N0648
Monotropein is an iridoid glycoside isolated. Monotropein inhibits theMorinda officinalis
expression of inflammatory mediators in dextransulfate sodium (DSS)-induced colitis mouse model.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
MorronisideCat. No.: HY-N0532
Morroniside has neuroprotective effect byinhibiting neuron apoptosis and MMP2/9 expression.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg
Mudanpioside CCat. No.: HY-N2163
Mudanpioside C is a monoteepenoid isolated from.Paeonia lactiflora Pall
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
MyricitrinCat. No.: HY-N0152
Myricitrin, isolated from Daebong persimmon peel,is a major antioxidant flavonoid.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Nagilactone BCat. No.: HY-N3216
Nagilactone B, extracted from the root bark of, is a liver X receptor ( )Podocarpus nagi LXR
agonist.
Purity: >98.0%Clinical Data: No Development ReportedSize: 1 mg
46 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Neoandrographolide (Neoandrographiside) Cat. No.: HY-N0721
Neoandrographolide is a diterpenoid from theAndrographis paniculata (Acanthaceae).
Purity: 99.65%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
NeocurdioneCat. No.: HY-N4243
Neocurdione is a hepatoprotective sesquiterpeneisolated from rhizome.Curcuma zedoariaNeocurdione exerts potent effect onD-galactosamine- (D-Gain) and lipopolysaccharide-(LPS) induced acute liver injury in mice.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
NeoisoliquiritigeninCat. No.: HY-N2121
Neoisoliquiritigenin, isolated from Spatholobus, inhibits cell proliferation and inducessuberectus
cell apoptosis in breast cancer by directlybinding to GRP78 to regulate the β-cateninpathway.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
NeotriptophenolideCat. No.: HY-N4082
Neotriptophenolide is a sesquiterpene pyridinealkaloid isolated from the root barks of
.Tripterygium hypoglaucum
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
NerolidolCat. No.: HY-N1944
Nerolidol is a natural membrane-activesesquiterpene, with antitumor, antibacterial,antifungal and antiparasitic activity.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
Nigranoic acidCat. No.: HY-122935
Nigranoic acid is a triterpenoid separated from. Nigranoic acid inhibits Schisandra chinensis HIV-1. Nigranoic acid exhibitsreverse transcriptase
protective effects on brain through PARP/AIFsignaling pathway in cerebral ischemia-reperfusionanimal model.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg
NimbinCat. No.: HY-N3187
Nimbin is a intermediate limonoid isolated from. Nimbin prevents aggregation andAzadirachta tau
increases cell viability. Nimbin is effectiveinhibits the .envelope protein of dengue virus
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
NimbolideCat. No.: HY-116035
Nimbolide is a triterpene derived from the leavesand flowers of neem ( L).Azadirachta indicaNimbolide induces apoptosis through inactivationof . Nimbolide inhibits / kinaseNF-κB CDK4 CDK6activity. Nimbolide suppresses the NF-κB, Wnt,PI3K-Akt, MAPK and JAK-STAT signaling pathways.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
NomilinCat. No.: HY-N0547
Nomilin is a limonoid compound obtained from theextracts of citrus fruits. Nomilin is ananti-obesity and anti-hyperglycemic agent .
Purity: 99.35%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Nootkatone ((+)-Nootkatone) Cat. No.: HY-N2195
Nootkatone, a neuroprotective agent from Alpiniae Fructus, has antioxidant andOxyphyllae
anti-inflammatory effects. Nootkatone improvescognitive impairment in lipopolysaccharide-inducedmouse model of Alzheimer's disease.
Purity: 99.35%Clinical Data: No Development ReportedSize: 100 mg
www.MedChemExpress.com 47
Notoginsenoside FaCat. No.: HY-N2530
Notoginsenoside Fa, a protopanaxadiol (ppd)-typesaponin isolated from , could possiblyP. notoginsengactivate and recover the function of degeneratedbrain.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Notoginsenoside FcCat. No.: HY-N2531
Notoginsenoside Fc, a protopanaxadiol- (PPD-) typesaponin isolated from the leaves of Panax
, effectively counteracts plateletnotoginsengaggregation. Notoginsenoside Fc can acceleratereendothelialization following vascular injury indiabetic rats by promoting .autophagy
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Notoginsenoside Fe (Notoginseng triterpenes; Ginsenoside Mb) Cat. No.: HY-N0046
Notoginsenoside Fe is a natural compound isolatedfrom Panax japlcus var.
Purity: 99.94%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Notoginsenoside FP2Cat. No.: HY-N4305
Notoginsenoside FP2, a dammarane-Type Bisdesmosideisolated from the Fruit Pedicels of Panax
, has potential to treat cardiovascularnotoginsengdisease.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Notoginsenoside Ft1Cat. No.: HY-N0910
Notoginsenoside Ft1 is a saponin isolated fromPanax notoginseng; stimulator of angiogenesis.
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Notoginsenoside R1 (Sanchinoside R1; Sanqi glucoside R1) Cat. No.: HY-N0615
Notoginsenoside R1, the main bioactive componentin panaxnotoginseng, is reported to have someneuronal protective, antihypertensive effects.
Purity: >97.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Notoginsenoside R2 (20(S)-Notoginsenoside R2; Ginsenoside Ng-R2) Cat. No.: HY-N0909
Notoginsenoside R2 is a newly isolatednotoginsenoside from Panax notoginseng, showedneuroprotective effects against 6-OHDA-inducedoxidative stress and apoptosis.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Notoginsenoside SCat. No.: HY-N5019
Notoginsenoside S is a compound isolated from Panax.notoginseng
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Nudicaucin ACat. No.: HY-N5087
Nudicaucin A is a triterpenoid saponin isolatedfrom .Hedyotis nudicaulis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Oleanolic Acid (Oleanic acid; Caryophyllin) Cat. No.: HY-N0156
Oleanolic acid (Caryophyllin) is a naturalcompound from plants with anti-tumor activities.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 100 mg, 500 mg
48 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Oleanonic acid (3-Oxooleanolic acid) Cat. No.: HY-N1487
Oleanonic acid (3-Oxooleanolic acid) is atriterpenoid, inhibits infection by HIV-1 in invitro infected PBMC, naturally infected PBMC andmonocyte/macrophages with of 22.7 mM, 24.6EC50
mM and 57.4 mM, respectively.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 50 mg
OleonuezhenideCat. No.: HY-N3145
Oleonuezhenide, isolated from Fructus LigustriLucidi, exerts neuroprotective effects.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
OleuropeinCat. No.: HY-N0292
Oleuropein, found in olive leaves and oil, exertsantioxidant, anti-inflammatory andanti-atherogenic effects through direct inhibitionof transcriptional activity.PPARγ
Purity: 98.54%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Ophiopogonoside ACat. No.: HY-N4274
Ophiopogonoside A is an eudesmane sesquiterpeneglycoside isolated from Liriope
.<br/>.muscari
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Orcinol glucosideCat. No.: HY-N0008
Orcinol glucoside (OG) is an active constituentisolated from , withRhizoma Curculiginisantidepressant effects. Orcinol glucosidefacilitates the shift of MSC fate to osteoblastand prevents adipogenesis via Wnt/β-cateninsignaling pathway.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Oridonin (NSC-250682; Isodonol) Cat. No.: HY-N0004
Oridonin (NSC-250682), a diterpenoid isolated from, acts as an inhibitor of ,Rabdosia rubescens AKT
with s of 8.4 and 8.9 μM for AKT1 and AKT2;IC50
Oridonin possesses anti-tumor, anti-bacterial andanti-inflammatory effects.
Purity: 99.85%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg, 200 mg, 500 mg
OrientinCat. No.: HY-N0405
Orientin is a naturally occurring bioactiveflavonoid that possesses diverse biologicalproperties, including anti-inflammation,anti-oxidative, anti-tumor, and cardio protection.Orientin is a promising neuroprotective agentsuitable for therapy for neuropathic pain.
Purity: 98.04%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
OxypaeoniflorinCat. No.: HY-N0748
Oxypaeoniflorin is a natural product derived fromRadix Paeoniae Rubra and Radix Paeoniae Alba.
Purity: 98.06%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Pachymic acid (3-O-Acetyltumulosic acid) Cat. No.: HY-N0371
Pachymic acid is a lanostrane-type triterpenoidfrom P. cocos. Pachymic acid inhibits andAkt
signaling pathways.ERK
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
PaclitaxelCat. No.: HY-B0015
Paclitaxel is a naturally occurring antineoplasticagent and stabilizes polymerization.tubulinPaclitaxel can cause both mitotic arrest and
cell death. Paclitaxel also inducesapoptotic.autophagy
Purity: 99.97%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg, 500 mg
www.MedChemExpress.com 49
PaederosideCat. No.: HY-N2432
Paederoside is a monoterpene S-methylthiocarbonate isolated from Paederia
. Paederoside shows a highpertomentosaanti-tumor promoting activity against the
activation.Epstein-Barr virus
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Paederosidic acidCat. No.: HY-N6998
Paederosidic acid is isolated from P. scandenswith anticancer and antiinflammation activities.Paederosidic acid inhibits lung caner cells viainducing mitochondria-mediated .apoptosis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Paederosidic acid methyl esterCat. No.: HY-N2433
Paederosidic acid methyl ester is a ATPsensitive activator, isolated fromK channel+
.P. scandens
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Paeoniflorin (Peoniflorin) Cat. No.: HY-N0293
Paeoniflorin (Peoniflorin), a heat shock-inducing compound and a pinane monoterpeneprotein
glycoside with various bioactivities, such asanticancer effects, anti-oxidative stress,antiplatelet aggregation, expansion of bloodvessels, reducing blood viscosity…
Purity: >98.0%Clinical Data: Phase 3Size: 10 mM × 1 mL, 100 mg, 200 mg
PalbinoneCat. No.: HY-N3115
Palbinone is a terpenoid isolated from the rootsof Pallas, potently inhibitsPaeonia albiflora
, with an3α-hydroxysteroid dehydrogenase (3α-HSD) of 46 nM. Anti-inflammatory activity.IC50
Purity: >98.0%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Palustric acidCat. No.: HY-133593
Palustric acid is a diterpenic resin acid found in.Pinus nigra
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Panaxadiol (20(R)-Panaxadiol) Cat. No.: HY-N0596
Panaxadiol is a novel antitumor agent extractedfrom the Chinese medical herb Panax ginseng.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
PanaxatriolCat. No.: HY-N0597
Panaxatriol is a natural product that can relievemyelosuppression induced by radiation injury.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg
ParishinCat. No.: HY-N2031
Parishin is a phenolic glucoside isolated from. Parishin exhibits antiaging effectsGastrodia elata
and extends the lifespan of yeast via regulationof signaling pathway.Sir2/Uth1/TOR
Purity: 99.10%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Parthenolide ((-)-Parthenolide) Cat. No.: HY-N0141
Parthenolide is a sesquiterpene lactone found inthe medicinal herb Feverfew. Parthenolide exhibitsanti-inflammatory activity by inhibiting NF-κBactivation; also inhibits protein withoutHDAC1affecting other class I/II HDACs.
Purity: 99.88%Clinical Data: Phase 2Size: 10 mM × 1 mL, 50 mg, 100 mg, 200 mg
50 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Patchouli alcoholCat. No.: HY-N0207
Patchouli alcohol is a natural tricyclicsesquiterpene extracted from Pogostemon cablin(Blanco) Benth, and exhibits anti-Helicobacter
and anti-inflammatory properties.pylori
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
PectolinarinCat. No.: HY-N0314
Pectolinarin, isolated from Cirsium, possesses anti-inflammatorychanroenicum
activity. Pectolinarin inhibits secretion of IL-6and , as well as the production of andIL-8 PGE2
.NO
Purity: 99.89%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
PedunculosideCat. No.: HY-N0458
Pedunculoside is a main bioactive componentisolated from Jiubiying. Pedunculoside exertslipid-lowering effects partly through theregulation of lipogenesis and fattyacid β-oxidation.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Perillyl alcoholCat. No.: HY-N7000
Perillyl alcohol is a monoterpene isolatedfrom the essential oils of lavendin, peppermint,spearmint, cherries, celery seeds, and severalother plants. Perillyl alcohol is active ininducing in tumor cells without affectingapoptosisnormal cells.
Purity: >95.0%Clinical Data: Phase 2Size: 100 mg
PhillyrinCat. No.: HY-N0482
Phillyrin is isolated from Forsythia suspensa Vahl(Oleaceae), has antibacterial andanti-inflammatory activities. Phillyrin haspotential inductive effects on rat andCYP1A2
activities, without affecting CYP2C11 andCYP2D1CYP3A1/2 activities.
Purity: 98.99%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
Phorbol (4β-Phorbol) Cat. No.: HY-N2147
Phorbol is a highly toxic diterpene, whose estershave important biological properties.
Purity: 99.32%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 1 mg, 5 mg, 10 mg, 25 mg, 50 mg
Phytol ((E)-Phytol) Cat. No.: HY-N3075
Phytol ((E)-Phytol), a diterpene alcohol fromchlorophyll widely used as a food additive and inmedicinal fields, possesses promisingantischistosomal properties.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
PhytolaccageninCat. No.: HY-N1433
Phytolaccagenin, a triterpenoid saponin, is theactive component of Radix Phytolaccae.Phytolcaccagenin has antifungal activity,anti-inflammatory activity and lower toxicity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Picfeltarraenin IACat. No.: HY-N1474
Picfeltarraenin IA, a triterpenoid obtained from Lour ( ), is anPicriafel-terrae P.fel-terrae
acetylcholinesterase ( ) inhibitor.AChEPicfeltarraenin IA can be used for the treatmentof herpes infections, cancer and inflammation.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Picfeltarraenin IBCat. No.: HY-N2211
Picfeltarraenin IB, a triterpenoid obtained from Lour ( ), is anPicriafel-terrae P.fel-terrae
acetylcholinesterase ( ) inhibitor.AChEPicfeltarraenin IB can be used for the treatmentof herpes infections, cancer and inflammation.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
www.MedChemExpress.com 51
Picfeltarraenin IVCat. No.: HY-N5076
Picfeltarraenin IV, a triterpenoid obtained from Lour ( ), is anPicriafel-terrae P.fel-terrae
acetylcholinesterase ( ) inhibitor.AChEPicfeltarraenin IV can be used for the treatmentof herpes infections, cancer and inflammation.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Picroside I (6'-Cinnamoylcatalpol) Cat. No.: HY-N0407
Picroside I is the major ingredient of Picrorhiza. Picrorhiza kurroa is a high value medicinalkurroa
herb due to rich source of hepatoprotectivemetabolites, Picroside-I and Picroside-II.Picroside I is a promising agent for themanagement of asthma.
Purity: 96.14%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
Picroside IICat. No.: HY-N0408
Picroside II, an iridoid compound extracted from, exhibits anti-inflammatory andPicrorhiza
anti-apoptotic activities. picroside II alleviatesthe inflammatory response in sepsis and enhancesimmune function by inhibiting the activation of
inflammasome and pathways.NLRP3 NF-κB
Purity: 99.77%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Picroside IIICat. No.: HY-N0409
Picroside III is an iridoid glycoside isolatedfrom (PS), aPicrorhiza scrophulariifloratraditional Chinese medicine.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
PlantamajosideCat. No.: HY-N0031
Plantamajoside is a phenylpropanoid glycosideisolated from (Plantaginaceae).Plantago asiatica L.Plantamajoside has protective effects onLPS-induced acute lung injury (ALI) mice model.Plantamajoside has the potential for the treatmentof pulmonary inflammation.
Purity: 95.42%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
PlaticodigeninCat. No.: HY-N1991
Platicodigenin isolated from platycodon.grandiflorum
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Platycodin DCat. No.: HY-N1411
Platycodin D is a saponin isolated from Platycodi, acts as an activator of , withRadix AMPKα
anti-obesity property.
Purity: 98.03%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Platycodin D2Cat. No.: HY-N4087
Platycodin D2 is a saponin isolated from Platycodon, with anti-cancer activity.grandiflorum
Purity: 99.36%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Platycodin D3Cat. No.: HY-N3519
Platycodin D3 is a triterpenoid saponin isolatedfrom , with anti-Platycodon grandiflorum HCVactivity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Platycoside ECat. No.: HY-N3522
Platycoside E is a platycodigenin-typesaponin isolated from the root of Platycodon
with andgrandiflorum haemolytic activity. Platycoside E promotes theadjuvant potential
production of the sera OVA-specific and IgG2a IgG2bantibody in the ovalbumin (OVA)-immunized mice.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
52 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Platycoside G1 (Deapi-platycoside E) Cat. No.: HY-N3521
Platycoside G1, a natural product found in, is a triterpenoidPlatycodon grandiflorum
saponin. Platycoside G1 has potent antioxidantactivities.
Purity: >98.0%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Pleuromutilin (Drosophilin B; Mutilin 14-glycolate) Cat. No.: HY-N2301
Pleuromutilin (Drosophilin B) inhibits bacterialprotein synthesis by binding to the 50S ribosomalsubunit of bacteria.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg, 500 mg
Podocarpic acidCat. No.: HY-N2318
Podocarpic acid is a natural product, which hasthe best all-round positive effect and acts as anovel activator.TRPA1
Purity: 99.56%Clinical Data: No Development ReportedSize: 10 mg, 50 mg
Polygalacin DCat. No.: HY-N6064
Polygalacin D (PGD) is a bioactive compoundisolated from Platycodon grandiflorum (Jacq.)with anticancer and anti-proliferativeproperties.
Purity: 99.30%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Polygalasaponin VCat. No.: HY-N2169
Polygalasaponin V is a triterpenoid saponinisolated from the aerial parts of .Polygala japonica
has been a folk medicine herb usedPolygala japonicaas expectorant, anti-inflammatory, antibacterialand antidepressant agents in the south of China.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Polygalaxanthone IIICat. No.: HY-N1407
Polygalaxanthone III is extracted from polygala, has inhibitory effect towardstenuifolia wild
enzyme. Polygalaxanthone III inhibitsCYP450chlorzoxazone 6-hydroxylation catalyzed by CYP2E1with an of 50.56 μM.IC50
Purity: 99.76%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Polyphyllin IICat. No.: HY-N0048
Polyphyllin II is one of the most significantsaponins in Rhizoma Paridis and has toxic effectson kinds of cancer cells. Polyphyllin II induces
through caspases activation andapoptosiscell-cycle arrest.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Polyporenic acid CCat. No.: HY-N2993
Polyporenic acid C is a lanostane-typetriterpenoid isolated from . PolyporenicP. cocosacid C induces cell through the deathapoptosisreceptor-mediated apoptotic pathway without theinvolvement of the mitochondria. Polyporenic acidC is promising agent for lung cancer therapy.
Purity: >99.0%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Ponicidin (Rubescensine B) Cat. No.: HY-N1535
Ponicidin (Rubescensine B) is a diterpenoidderived from , and exhibitsRabdosia rubescensimmunoregulatory, anti-inflammatory, anti-viraland anti-cancer activity.
Purity: 99.79%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Pristimerin (Celastrol methyl ester) Cat. No.: HY-N1937
Pristimerin is a potent and reversiblemonoacylglycerol lipase ( ) inhibitor with anMGL
of 93 nM.IC50
Purity: 99.64%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg
www.MedChemExpress.com 53
Pseudoginsenoside F11 (Ginsenoside A1) Cat. No.: HY-N0541
Pseudoginsenoside F11 (Ginsenoside A1), acomponent of Panax quinquefolium (Americanginseng), has been demonstrated to antagonize thelearning and memory deficits induced byscopolamine, morphine and methamphetamine in mice.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Pseudoginsenoside RT1Cat. No.: HY-N2201
Pseudoginsenoside RT1, isolated from the fruit ofRandia siamensis, exhibits acute ichthyotoxicactivity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Pseudoginsenoside RT5Cat. No.: HY-N0542
Pseudoginsenoside RT5 is isolated from Panax.quinquefolium
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Pseudolaric Acid ACat. No.: HY-N0673
Pseudolaric Acid A is a diterpene acid isolatedfrom , has antifungal,Pseudolarix kaempfericytotoxic and antifertile activities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Pseudolaric Acid BCat. No.: HY-N6939
Pseudolaric Acid B is a diterpene isolated fromthe root of GordenPseudolarix kaempferi(pinaceae), has anti-cancer, antifungal, andantifertile activities, and showsimmunosuppressive activity on T lymphocytes.
Purity: 99.47%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Pseudolaric acid B β-D-glucosideCat. No.: HY-N6938
Pseudolaric acid B β-D-glucoside is a diterpenoidisolated from .Pseudolarix kaempferi
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Pseudolaric Acid CCat. No.: HY-N0672
Pseudolaric C is a diterpenoid isolated from theroot bark of Gorden, hasPseudolarix kaempferiantifungal activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Pseudolaric Acid C2Cat. No.: HY-N6910
Pseudolaric Acid C2, a diterpenoid isolated from, is identified as thePseudolarix kaempferi
specific metabolite of Pseudolaric acid B inplasma, urine, bile and feces after both oral andintravenous administration to rats.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Pulchinenoside A (Anemoside A3) Cat. No.: HY-N0204
Pulchinenoside A is a natural triterpenoid saponinthat enhances synaptic plasticity in the adultmouse hippocampus and facilitates spatial memoryin adult mice.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Pulchinenoside C (Anemoside B4) Cat. No.: HY-N0205
Pulchinenoside C (Anemoside B4) is Pulsatillakoreana Nakai that have many numerous biologicaleffects in vitro, including enhancinghypoglycemic, anti-tumor, neuroprotective andanti-angiogenic activity.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
54 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Pulsatilla saponin D (SB365; Hederacolchiside A) Cat. No.: HY-N0834
Pulsatilla saponin D (SB365), isolated from theroot of Nakai, is an anti-tumorPulsatilla koreanaagent.
Purity: 98.47%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg
PunicalaginCat. No.: HY-N0063
Punicalagin is a polyphenol ingredient isolatedfrom Pomegranate ( L.) or thePunica granatumleaves of L.. Punicalagin isTerminalia catappaa agent and hasanti-hepatitis B virus (HBV)antioxidant, anti-inflammatory, and anticancereffects.
Purity: 99.80%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Quassin (Nigakilactone D) Cat. No.: HY-N1581
Quassin (Nigakilactone D) is a bioactivetriterpenoid from stem bark extract of Quassia
. Quassin inhibits with anamara P. falciparum of 0.15 μM. Quassin possesses reversibleIC50
antifertility, anti-estrogenic and anti-plasmodialactivity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Quillaic acid (Quillaja sapogenin) Cat. No.: HY-N0839
Quillaic acid(Quillaja sapogenin) is the majoraglycone of the widely studied saponins of theChilean indigenous tree Quillaja saponaria Mol;can elicit dose-dependent antinociceptive effectsin two murine thermal models.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Raddeanin ACat. No.: HY-N0819
Raddeanin A is a natural triterpenoid saponincomponent of , with anti-cancerAnemone raddeanaactivities. Raddeanin A exerts anticancer effecton human osteosarcoma via the ROS/JNK and NF-κBsignal pathway.
Purity: 98.04%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Rebaudioside ACat. No.: HY-N0466
Rebaudioside A is a steviol glycoside,α-glucosidase inhibitor with IC50 of 35.01μg/ml.can inhibit ATP-sensitive K+-channels.
Purity: >98.0%Clinical Data: Phase 1Size: 10 mM × 1 mL, 100 mg, 500 mg
Rebaudioside C (Dulcoside B) Cat. No.: HY-N0467
Rebaudioside C(Dulcoside B) is used as naturalsweeteners to diabetics and others oncarbohydrate-controlled diets.
Purity: 96.39%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Rebaudioside DCat. No.: HY-N0468
Rebaudioside D is a glycoside found in the leavesof and acts as a sweetener.Stevia rebaudiana
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Rehmannioside CCat. No.: HY-N2400
Rehmannioside C is an iridoid glucoside isolatedfrom Radix .Rehmanniae Praeparata
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Rehmannioside DCat. No.: HY-N0912
Rehmannioside D is a carotenoid glycoside.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
www.MedChemExpress.com 55
RehmapicrosideCat. No.: HY-N2398
Rehmapicroside is an ionone glycoside isolatedfrom rhizomes of .Rehmannia glutinosa
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Retinyl acetate (Retinol acetate; Vitamin A acetate) Cat. No.: HY-N0679
Retinyl acetate is a synthetic acetate ester formderived from retinol and has potentialantineoplastic and chemo preventive activities.
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg, 500 mg
Rhodojaponin IICat. No.: HY-N2151
Rhodojaponin II is a diterpenoid from the leavesof with anti-inflammatoryRhododendron molleactivity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Rhodojaponin IIICat. No.: HY-N2152
Rhodojaponin III is a diterpenoid from the leavesof with anti-inflammatoryRhododendron molleactivity.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Rhodojaponin VCat. No.: HY-N2154
Rhodojaponin V is a diterpenoid from the leaves of with anti-inflammatoryRhododendron molle
activity.
Purity: >99.0%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Roburic acidCat. No.: HY-N0481
Roburic acid, a tetracyclic triterpenoid found in, acts as an inhibitor ofGentiana macrophylla
, with s of 5 and 9 μM for COX-1 andCOX IC50
COX-2, respectively.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
RosamultinCat. No.: HY-N2565
Rosamultin is a 19 α-hydroxyursane-typetriterpenoid isolated from Potentilla
. Rosamultin has inhibitory effectsanserina Lagainst .HIV-1 protease
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
RosarinCat. No.: HY-N0506
Rosarin is a cinnamyl alcohol glycosideisolated from . Rosarin hasRhodiola roseaanti-inflammatory and effects.neuroprotective
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
RosavinCat. No.: HY-N0507
Rosavin is isolated from , Rosavin showsR. roseaantidepressant-like, adaptogenic, anxiolytic-likeeffects in mice model.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
RosinCat. No.: HY-N0508
Rosin is isolated from pine wood or pine stumps,Rosin is a frequent contact which inducesallergenallergic contact dermatitis.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
56 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
RosiridinCat. No.: HY-N0505
Rosiridin, which is isolated from L.,Rhodiola roseainhibits and with potentialMAO A MAO Bbeneficial effect in depression and seniledementia. Rosiridin shows an inhibition of 83.8%against MAO B at 10 μM (pIC =5.38).50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg, 10 mg
Rosmarinic acid (Labiatenic acid) Cat. No.: HY-N0529
Rosmarinic acid is a widespread phenolic estercompound in the plants. Rosmarinic acid inhibits
, and enzymes with sMAO-A MAO-B COMT IC50
of 50.1, 184.6 and 26.7 μM, respectively.
Purity: 99.29%Clinical Data: Phase 4Size: 10 mM × 1 mL, 50 mg, 100 mg
Rotundic acidCat. No.: HY-N2217
Rotundic acid, a triterpenoid obtained from I., induces DNA damage and cell apoptosis inrotunda
hepatocellular carcinoma through andAKT/mTOR Pathways. Rotundic acid possessesMAPK
anti-inflammatory and cardio-protective abilities.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
RotundifuranCat. No.: HY-116894
Rotundifuran, a labdane type diterpene, isisolated from . Rotundifuran canVitex rotundifoliainhibit the cell cycle progression and induceapoptosis in human myeloid leukaemia cells.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg
RubusosideCat. No.: HY-N0668
Rubusoside is a natural sweetener and asolubilizing agent with antiangiogenic andantiallergic properties. Rubusoside is anexcellent solubilizing agent.
Purity: 98.58%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
Rupestonic acidCat. No.: HY-N3016
Rupestonic acid, a sesquiterpene from Artemisia L., can inhibit .rupestris influenza virus
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
RuscogeninCat. No.: HY-N0496
Ruscogenin, an important steroid sapogenin derivedfrom Ophiopogon japonicus, attenuates cerebralischemia-induced blood-brain barrier dysfunctionby suppressing TXNIP/NLRP3 inflammasome activationand the MAPK pathway and exerts significantanti-inflammatory and anti-thrombotic activities.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg
RutaevinCat. No.: HY-N2620
Rutaevin is isolated from the fruits of Euodia. Rutaevin inhibits inrutaecarpa NO production
LPS-induced RAW 264.7 macrophages.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
RyanodineCat. No.: HY-103306
Ryanodine is a cell permeant ryanodine receptormodulator. Ryanodine can either stimulate orinhibit Ryanodine-mediated Ca release depending2+
on its concentrations. Poisonous diterpenoid foundin .Ryania speciosa
Purity: >98.0%Clinical Data: No Development ReportedSize: 1 mg
Saikogenin ACat. No.: HY-N6584
Saikogenin A, extracted from a Chinese herbalplant called Tsai-Fu, is a dipeptidyl peptidase-IV( ) inhibitor.DPP-IV
Purity: 98.31%Clinical Data: No Development ReportedSize: 5 mg
www.MedChemExpress.com 57
Saikosaponin ACat. No.: HY-N0246
Saikosaponin A is an active component of, up-regulates Bupleurum falcatum LXRα
expression, with potent anti-inflammatoryactivity.
Purity: 99.43%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
Saikosaponin B1Cat. No.: HY-N0247
Saikosaponin B1 is a component of Saiko, enhancesthe effect of cancer chemotherapy.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Saikosaponin B2Cat. No.: HY-N0248
Saikosaponin B2 is an active component from root, acts as an entry inhibitorBupleurum kaoi
against HCV infection. Anti-cancer activity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Saikosaponin B3Cat. No.: HY-N4219
Saikosaponin B3 is a saikosaponin isolated fromthe roots of , withBupleurum falcatum L.analgesic effect. Saikosaponin B3 inhibitsACTH-induced lipolysis in the fat cells.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Saikosaponin B4Cat. No.: HY-N4218
Saikosaponin B4 is a member of saikosaponinsisolated from the roots of ,B. falcatumselectively inhibits ACTH-induced lipolysis.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Saikosaponin CCat. No.: HY-N0249
Saikosaponin C is a bioactive component found in, targets and inradix bupleuri amyloid beta tau
Alzheimer's disease. Saikosaponin C inhibits thesecretion of both Aβ1-40 and Aβ1-42, andsuppresses abnormal tau phosphorylation, but showsno effect on BACE1 activity and expression.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Saikosaponin DCat. No.: HY-N0250
Saikosaponin D is a triterpene saponin isolatedfrom Bupleurum, with anti-inflammatory,anti-bacterial, anti-tumor, and anti-allergicactivities; Saikosaponin D inhibits ,selectin
and and activates STAT3 NF-kB estrogen.receptor-β
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg
Saikosaponin ECat. No.: HY-N4211
Saikosaponin E is a saikosaponin isolated from.Bupleurum yinchowense
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Saikosaponin FCat. No.: HY-N2178
Saikosaponin F is a component found in.Bupleurum (B.) falcatum L
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Saikosaponin GCat. No.: HY-N4216
Saikosaponin G is a triterpene glycoside isolatedfrom .Bupleuri Radix
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
58 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Saikosaponin HCat. No.: HY-N2603
Saikosaponin H is a saikosaponin derived from theherb .Radix bupleuri
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
SalanninCat. No.: HY-123026
Salannin, a limonoid bitter principle of the seedoil of , shows antiulcer andAzadirachta indicaspermicidal activities. Salannin displaysantibacterial activity towards both Gram-positiveand Gram-negative bacteria.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Sandaracopimaric acidCat. No.: HY-133594
Sandaracopimaric acid is a diterpenoid withanti-inflammatory effect. Sandaracopimaric acidreduces the contraction of phenylephrine-inducedpulmonary arteries with an of 43.93 μM.EC50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Santonin (Alpha-Santonin) Cat. No.: HY-B1761
Santonin is an active principle of the plant, which is formely used to treatArtemisia cina
worms.
Purity: 99.80%Clinical Data: LaunchedSize: 10 mM × 1 mL, 500 mg
ScabertopinCat. No.: HY-N1247
Scabertopin, isolated from the whole plant of, is a sesquiterpene lactone.Elephantopus scaber
Scabertopin has been found to be prominentanticancer constituents.
Purity: >99.0%Clinical Data: No Development ReportedSize: 5 mg
Sclareol glycolCat. No.: HY-N7007
Sclareol glycol is the precursor of ambroxide. ATCC 20624 was the onlyHyphozyma roseonigra
reported strain capable of degrading sclareol tothe main product of sclareol glycol.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
ScopolinCat. No.: HY-N0341
Scopolin is a coumarin isolated from Arabidopsis (Arabidopsis) roots. Scopolin attenuatedthaliana
hepatic steatosis through activation of-mediated signaling cascades.SIRT1
Purity: >99.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg
SecaubryenolCat. No.: HY-N1272
Secaubryenol is a class of 3,4-secocycloartanetriterpenes isolated from Coussarea macrophylla.Secaubryenol does not display any cytotoxic effect
.at a dose of 10 µg/mL.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
SecologanosideCat. No.: HY-N6876
Secologanoside is a triterpenoid isolated from, weakly inhibits with anPoraqueiba sericea elastase
of 164 μg/mL. Secologanoside is moderateIC50
cytotoxic to fibroblasts.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
SesamosideCat. No.: HY-N0412
Sesamoside is a iridoid isolated from the aerialpart of . SesamosidePhlomis linearifoliahas antiodant and antiglycation activities.
Purity: 98.74%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
www.MedChemExpress.com 59
Shanzhiside methyl esterCat. No.: HY-N0630
Shanzhiside methy lester is isolated from .L. rotataShanzhiside methyl ester is a small molecule
agonistglucagon-like peptide-1 (GLP-1) receptorand has the ability to induce anti-allodynictolerance.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
ShiononeCat. No.: HY-N0829
Shionone is the major triterpenoid isolated from, has anti-tussive, anti-inflammatoryAster tataricus
activities. Shionone possesses a uniquesix-membered tetracyclic skeleton and3-oxo-4-monomethyl structure.
Purity: >98.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Siamenoside ICat. No.: HY-N0612
Siamenoside I is one of the mogrosides that hasseveral kinds of bioactivities.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Simvastatin (MK 733) Cat. No.: HY-17502
Simvastatin (MK 733) is a competitive inhibitor of with a of 0.2 nM.HMG-CoA reductase Ki
Purity: 99.81%Clinical Data: LaunchedSize: 50 mg, 100 mg, 200 mg, 500 mg
SinigrinCat. No.: HY-N0404
Sinigrin is a major glucosinolate present inplants of the family, withBrassicaceaeanti-adipogenic effects.
Purity: 99.74%Clinical Data: No Development ReportedSize: 10 mg, 25 mg, 50 mg, 100 mg
Siraitic Acid ACat. No.: HY-N6917
Siraitic Acid A is a cucurbitane triterpenoidisolated from the root of .S. grosvenori
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Siraitic Acid BCat. No.: HY-N6916
Siraitic Acid B is a cucurbitane triterpenoidisolated from the root of .S. grosvenori
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Sodium aescinateCat. No.: HY-N1404
Sodium aescinate is a triterpene saponin derivedfrom seeds, withAesculus hippocastanumanti-inflammatory and antioxidant activities.Sodium aescinate inhibits hepatocellular carcinomagrowth by targeting CARMA3/NF-κB pathway.
Purity: >98%Clinical Data: LaunchedSize: 1 mg, 5 mg
Soyasapogenol ACat. No.: HY-N6073
Soyasapogenol A, a triterpene compound, isolatedfrom the roots of .Abrus cantoniensis
Purity: 99.06%Clinical Data: No Development ReportedSize: 5 mg
Soyasapogenol BCat. No.: HY-N6074
Soyasapogenol B, an ingredient of soybean, exertsanti-proliferative, anti-metastatic activities.Soyasapogenol B triggers endoplasmic reticulumstress, which mediates and inapoptosis autophagycolorectal cancer.
Purity: 98.26%Clinical Data: No Development ReportedSize: 1 mg, 5 mg, 10 mg
60 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Soyasaponin AcCat. No.: HY-N6999
Soyasaponin Ac is a triterpenoid isolated from theseeds of Glycine max.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Soyasaponin IICat. No.: HY-122920
Soyasaponin II is a saponin with antiviralactivity. Soyasaponin II inhibits the replicationof HSV-1, HCMV, influenza virus, and HIV-1.Soyasaponin II shows potent inhibition on HSV-1replication.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg
Soyasaponin IIICat. No.: HY-N7273
Soyasaponin III, a monodesmodic oleananetriterpenoid, is one of the main potentiallybioactive saponins found in soy ( )Glycine maxand related products. Soyasaponin III can induce
in Hep-G2 cells.apoptosis
Purity: >95.0%Clinical Data: No Development ReportedSize: 1 mg
SpathulenolCat. No.: HY-N1205
Spathulenol is isolated from Psidium guineense, and has antioxidant, anti-inflammatory,Sw
antiproliferative and antimycobacterialactivities. Spathulenol shows a high antioxidantactivity with an of 85.60 μg/mL in the DPPHIC50
system ..
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Specnuezhenide ((8E)-Nuezhenide) Cat. No.: HY-N0665
Specnuezhenide ((8E)-Nuezhenide) is isolated fromthe fruits of .Ligustrum lucidumSpecnuezhenide ((8E)-Nuezhenide) can inhibitIL-1β-induced inflammation in chondrocytes viainhibition of and NF-κB wnt/β-cateninsignaling.
Purity: 98.55%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 25 mg
Squalene (Super Squalene; trans-Squalene; AddaVax) Cat. No.: HY-N1214
Squalene is an intermediate product in thesynthesis of cholesterol, and shows severalpharmacological properties such as hypolipidemic,hepatoprotective, cardioprotective, antioxidant,and antitoxicant activity.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 5 mg, 10 mg
Stearyl glycyrrhetinateCat. No.: HY-N2417
Stearyl glycyrrhetinate, a major component inlicorice extract, has a MIC against S. aureusstrains of more than 256 mg/L. Stearylglycyrrhetinate has effects.antibacterial
Purity: >98%Clinical Data: No Development ReportedSize: 500 mg
SteviolCat. No.: HY-N2057
Steviol is a major metabolite of the sweeteningcompound stevioside. Steviol slows renal cystgrowth by reducing AQP2 expression and promotingAQP2 degradation.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Steviol-19-O-glucosideCat. No.: HY-N6918
Steviol-19-O-glucoside is a metabolite ofsteviol in the steviol glycosides biosynthesispathway in .Stevia rebuadiana
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
SteviolbiosideCat. No.: HY-N2547
Steviolbioside is a rare sweetener that exists instevia rebaudiana leaves. Steviolbioside presentsinhibition on several human cancer cells and actsas potential remedy for human breast cancer.
Purity: 98.19%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
www.MedChemExpress.com 61
SteviosideCat. No.: HY-N0669
Stevioside is a natural sweetener extracted fromleaves of , with anticancerStevia rebaudianaactivity.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Suavissimoside R1Cat. No.: HY-N7025
Suavissimoside R1, isolated from the roots ofRubus parvifollus, possesses potentneuroprotective activity and has the potential totreat anti-Parkinson's disease drug.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
SwerosideCat. No.: HY-N0806
Sweroside, isolated from Lonicera japonica,exhibits cytoprotective, anti-osteoporotic, andhepatoprotective effect.
Purity: 99.84%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
SwertiamarinCat. No.: HY-N0807
Swertiamarin, a secoiridoid glycoside found ingenera of , confersEnicostemma Speciesanti-hyperglycemic and anti-hyperlipidemiceffects.
Purity: 98.43%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
TaraxasterolCat. No.: HY-N1178
Taraxasterol is a pentacyclic triterpenoidisolated from Taraxacum officinale. Taraxasterolhas a role as a metabolite and ananti-inflammatory agent.
Purity: 99.33%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Taraxasteryl acetateCat. No.: HY-N2478
Taraxasteryl acetate is isolated from P.,and has a broad spectrum ofsagittalis
activity. Taraxasterylanti-inflammatoryacetate relieves dextran, zymosan and arachidonicacid induced rat hind-paw edema.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
TaraxerolCat. No.: HY-N2477
Taraxerol is isolated from , andAbroma augusta Lhas anti-inflammtory and anti-cancer effects.Taraxerol attenuates acute inlammation throughinhibition of signaling pathway. TaraxerolNF-κBinduces cell .apoptosis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg, 10 mg
Taraxerol acetateCat. No.: HY-N2599
Taraxerol acetate is a and inhibitorCOX-1 COX-2with IC values of 116.3 μM and 94.7 μM,50
respectively. Taraxerol acetate the has theanticancer potential and induces cell
.</br>.apoptosis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
TaraxeroneCat. No.: HY-N1177
Taraxerone is isolated from Sedum. Taraxerone enhances effects onsarmentosum
alcohol dehydrogenase ( ) and acetaldehydeADHdehydrogenase ( ) activities with ALDH EC50
values of 512.42 and 500.16 μM, respectively.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
TenuifolinCat. No.: HY-N0702
Tenuifolin is a triterpene isolated from Polygala, has neuroprotectivetenuifolia Willd
effects. Tenuifolin reduces Aβ secretion byinhibiting .β-secretase
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
62 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
Tenuigenin (Senegenin) Cat. No.: HY-N0802
Tenuigenin is a major active component isolatedfrom the root of the Chinese herb Polygala
. Tenuigenin protects againsttenuifoliaS.aureus-induced pneumonia by inhibiting NF-κBactivation. Tenuigenin has anti-inflammatoryeffect.
Purity: 99.24%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Terpinen-4-ol (4-Carvomenthenol) Cat. No.: HY-W017316
Terpinen-4-ol (4-Carvomenthenol), a naturallyoccurring monoterpene, is the main bioactivecomponent of tea-tree oil. Terpinen-4-olsuppresses inflammatory mediator production byactivated human monocytes.
Purity: >96.0%Clinical Data: Phase 1Size: 10 mM × 1 mL, 100 mg
TeucvidinCat. No.: HY-N2525
Teucvidin is a diterpenoid from Teucriumspecies.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Tiamulin (Thiamutilin) Cat. No.: HY-B2060
Tiamulin (Thiamutilin) is a diterpenic compoundthat widely used in swine for the control ofinfectious diseases, including swine dysentery andenzootic pneumonia.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
ToosendaninCat. No.: HY-N0263
Toosendanin, a triterpenoid extracted from thebark of fruit of Melia toosendan Sieb et Zucc,possesses analgesic, insecticidal andanti-inflammatory activities.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 20 mg
TrachelosideCat. No.: HY-N1507
Tracheloside is an antiestrogenic lignin.Tracheloside promotes keratinocyte proliferationthrough ERK1/2 stimulation. Tracheloside is a goodcandidate to promote wound healing.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Transcrocetin (trans-Crocetin) Cat. No.: HY-N2072
Transcrocetin (trans-Crocetin), extracted fromsaffron ( ), acts as an Crocus sativus L. NMDA
antagonist with high affinity.receptorTranscrocetin (trans-Crocetin) is capable ofcrossing the blood-brain barrier and reach thecentral nervous system (CNS).
Purity: 98.60%Clinical Data: Phase 2Size: 5 mg, 10 mg
Transcrocetin meglumine salt (trans-Crocetin meglumine salt) Cat. No.: HY-42937
Transcrocetin meglumine salt, extracted fromsaffron ( ), acts as an Crocus sativus L. NMDA
antagonist with high affinity.receptor
Purity: 95.13%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg
Tripterin (Celastrol) Cat. No.: HY-13067
Tripterin (Celastrol) is a inhibitorproteasomewhich potently and preferentially inhibits thechymotrypsin-like activity of a purified 20S
with of 2.5 μM.proteasome IC50
Purity: 99.91%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg, 100 mg
Triptolide (PG490) Cat. No.: HY-32735
Triptolide is a diterpenoid triepoxide extractedfrom the root of withTripterygium wilfordiiimmunosuppressive, anti-inflammatory andantiproliferative effects. Triptolide is a NF-κBactivation inhibitor.
Purity: 99.79%Clinical Data: LaunchedSize: 10 mM × 1 mL, 2 mg, 5 mg, 10 mg, 25 mg, 100 mg
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Triptonide (NSC 165677; PG 492) Cat. No.: HY-32736
Triptonide(NSC 165677; PG 492), extracted fromTripterygium wilfordii Hook, inhibited theproliferation of mouse splenocytes induced bysuboptimal concentration of concanavalin A orlipopolysaccharide at concentrations of 0.02, 0.1,and 0.5 mg/ml.
Purity: 98.65%Clinical Data: LaunchedSize: 10 mM × 1 mL, 10 mg
Triptophenolide (Hypolide; (+)-Triptophenolide) Cat. No.: HY-N0475
Triptophenolide is a colorless crystalline plateisolated from ethyl acetate extracts ofTripterygium wilfordii.
Purity: 99.93%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Tubeimoside I (Tubeimoside-1; Lobatoside-H) Cat. No.: HY-N0890
Tubeimoside I(Lobatoside-H) is an extract fromChinese herbal medicine Bolbostemma paniculatum(MAXIM.) FRANQUET (Cucurbitaceae) has been shownas a potent anti-tumor agent for a variety ofhuman cancers.
Purity: 98.03%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 10 mg, 50 mg
Tubeimoside II (Tubeimoside-B) Cat. No.: HY-N0891
Tubeimoside II(Tubeimoside-B) is a naturalanalogue of oleanane type of triterpenoid saponin;show anti-inflammatory, antitumor, andantitumor-promoting effects.
Purity: 99.70%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
Tubeimoside IIICat. No.: HY-N2542
Tubeimoside III, a triterpenoid saponin isolatedfrom a Chinese folk medicine"Tubeimu", showsanti-inflammatory, anti-tumor, anti-tumorigenicactivities, and acute toxicity in vivo.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
TussilagoneCat. No.: HY-N1388
Tussilagone, a major active component in Tussilago, has anti-inflammatory effect. Tussilagonefarfara
ameliorates inflammatory responses in dextransulphate sodium-induced murine colitis.
Purity: 99.51%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Ursolic acid (Prunol; Urson; Malol) Cat. No.: HY-N0140
Ursolic acid (Prunol) is a natural pentacyclictriterpenoid carboxylic acid, exerts anti-tumoreffects and is an effective compound for cancerprevention and therapy.
Purity: 99.27%Clinical Data: Phase 2Size: 10 mM × 1 mL, 5 mg, 10 mg
Ursolic acid acetate (Acetylursolic acid; 3-Acetylursolic acid) Cat. No.: HY-N2815
Ursolic acid acetate (Acetylursolic acid),isolated from the aerial roots of Ficus
, exhibits cytotoxicity against KBmicrocarpacells with of 8.4 μM.IC50
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
Ursonic acid (3-Ketoursolic acid) Cat. No.: HY-N1486
Ursolic acid, a naturally occurring triterpenoid,induces the apoptosis of human cancer cellsthrough multiple signaling pathways.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg
UvaolCat. No.: HY-N1109
Uvaol, a triterpene present in olives and virginolive oil, possesses anti-inflammatory propertiesand antioxidant effects. Uvaol attenuatespleuritis and eosinophilic inflammation inovalbumin-induced allergy in mice.
Purity: >95.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
64 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
ValenceneCat. No.: HY-N6636
Valencene is a sesquiterpene isolated from Cyperus, possesses antiallergic,rotundus
antimelanogenesis, anti-infammatory, andantioxidant activitivies.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Valepotriate (Valtrate) Cat. No.: HY-N0718
Valepotriate, isolated from Valeriana Jones, has anti-epileptic andjatamansi
anti-cancer activities.
Purity: 97.24%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
VerbenalinCat. No.: HY-N2014
Verbenalin is Verbena glycoside, withanti-inflammatory, anti-fungal anti-virusactivities. Verbenalin can be used for theresearch of prostatitis. Verbenalin can reducecerebral ischemia-reperfusion injury.
Purity: 99.47%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 25 mg
Verbenone ((-)-Verbenone) Cat. No.: HY-N6661
Verbenone ((-)-Verbenone) is a natural terpene inleaves of the tree, Verdc.Suregada zanzibariensisVerbenone has anti-aggregation pheromone andinterrupts the attraction of bark beetles to theiraggregation pheromones.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
VerminosideCat. No.: HY-N1094
Verminoside is an iridoid isolated from Kigelia, exhibits anti-inflammatory and remarkableafricana
antioxidant activity with a radical-scavengingactivity of 2.5 μg/mL. The genotoxicity ofVerminoside on human lymphocytes is associatedwith elevated levels of and proteins.PARP-1 p53
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Vinaginsenoside R4Cat. No.: HY-N4265
Vinaginsenoside R4, isolated from the leaves ofhydroponic . It has an inhibitoryPanax ginsengeffect on melanin biosynthesis without anycytotoxic effects on the melan-a cells, andenhances the depigmentation on the zebrafish.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Vinaginsenoside R8Cat. No.: HY-N4266
Vinaginsenoside R8, a triterpenoid glycosideisolated from the rhizomes of .Panacis majorisVinaginsenoside R8 displays activities againstadenosine diphosphate (ADP)-induced plateletaggregation ( =25.18 μM).IC50
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
WaltonitoneCat. No.: HY-128366
Waltonitone is a ursane-type pentacyclictriterpene isolated from Gentian waltoniiBurkill. Waltonitone significantly inhibitshepatocellular carcinoma cells growth and induces
in vitro and in vivo.apoptosis
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
WilforgineCat. No.: HY-N1072
Wilforgine is a bioactive sesquiterpene alkaloidin Hook. F.Tripterygium wilfordii
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
Wilforlide A (Regelide; Abruslactone A) Cat. No.: HY-N0476
Wilforlide A is a natural product, separated fromthe ethanolic extract of tripterygium wilfordii.
Purity: >99.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
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XanthatinCat. No.: HY-N3032
Xanthatin is isolated from Xanthium leaves.strumarium
Purity: 99.79%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg, 100 mg
XanthorrhizolCat. No.: HY-112657
Xanthorrhizol, isolated from Curcuma Roxb, is a potential antibacterialxanthorrhiza
agent.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
Yamogenin (Neodiosgenin) Cat. No.: HY-N2078
Yamogenin (Neodiosgenin) is a diastereomer ofdiosgenin. Yamogenin (Neodiosgenin) antagonizesthe activation of the liver X receptor (LXR) inluciferase ligand assay.
Purity: 99.20%Clinical Data: No Development ReportedSize: 10 mg, 25 mg
Yuanhuacine (Gnidilatidin) Cat. No.: HY-N7225
Yuanhuacine (Gnidilatidin), a daphnane diterpenoidfrom the flowers of Daphne genkwa with extensiveanti-tumor activity. Yuanhuacine is a DNA-damagingagent with orally active.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg
Zingiberen NewsaponinCat. No.: HY-N2282
Zingiberen Newsaponin is extracted from isolatedfrom . Zingiberen NewsaponinDioscorea zingiberensisexhibits induction effect on platelet aggregation.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg, 10 mg
Zingiberene (α-Zingiberene; (-)-Zingiberene) Cat. No.: HY-14618
Zingiberene (α-Zingiberene) is a monocyclicsesquiterpene which is the predominant constituentof ginger with oil content ( ).Zingiber officinaleNeuroprotective potential. Zingiberene triggers
. Anticancer activity.autophagy
Purity: >97.0%Clinical Data: No Development ReportedSize: 5 mg
Zingibroside R1Cat. No.: HY-N6924
Zingibroside R1 is dammaranae-type triterpenoidsaponin, isolated from rhizomes, taproots, andlateral roots of C. A. Meyer, showsPanax japonicasexcellent anti-tumor effects as well asanti-angiogenic activity. Zingibroside R1possesses some anti- activity.HIV-1
Purity: >98%Clinical Data:Size: 5 mg, 10 mg
Ziyuglycoside ICat. No.: HY-N0331
Ziyuglycoside I isolated from root,S. officinalishas anti-wrinkle activity, and increases theexpression of type I collagen. Ziyuglycoside Icould be used as an active ingredient forcosmetics.
Purity: 98.51%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 5 mg, 10 mg, 25 mg, 50 mg
Ziyuglycoside IICat. No.: HY-N0332
Ziyuglycoside II is a triterpenoid saponincompound extracted from L..Sanguisorba officinalisZiyuglycoside II induces reactive oxygen species( ) production and . Anti-inflammationROS apoptosisand anti-cancer effect.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg, 10 mg
α-Amyrin acetateCat. No.: HY-N2842
α-Amyrin acetate, a natural triterpenoid, hasanti-inflammatory activity, antispasmodic profileand the relaxant effect.
Purity: >98%Clinical Data: No Development ReportedSize: 5 mg
66 Tel: 609-228-6898 Fax: 609-228-5909 Email: [email protected]
α-Humulene (Humulene; α-Caryophyllene) Cat. No.: HY-N6968
α-Humulene is a main constituent of Tanacetum L. (Asteraceae) essential oil withvulgare
anti-inflammation (IC =15±2 µg/mL). α-Humulene50
inhibits and expression.COX-2 iNOS
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
α-TerpineolCat. No.: HY-N5142
α-Terpineol is isolated from Eucalyptus globulus, exhibits strong antimicrobial activityLabill
against periodontopathic and cariogenic bacteria.α-Terpineol possesses antifungal activity against
, and the activity might leadT. mentagrophytesto irreversible cellular disruption.
Purity: >98.0%Clinical Data: No Development ReportedSize: 10 mM × 1 mL, 100 mg
α-ThujoneCat. No.: HY-121618
α-Thujone is a monoterpene isolated from Thuja essential oil with potent anti-tumoroccidentalis
activities. α-Thujone is a reversible modulator ofthe and the forGABA type A receptor IC50
α-Thujone is 21 μM in suppressing the -inducedGABAcurrents.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
β-Carotene (Provitamin A; beta-Carotene) Cat. No.: HY-N0411
β-Carotene (Provitamin A) is an organic compoundand classified as a terpenoid. It is a precursor(inactive form) of vitamin A.
Purity: >98.0%Clinical Data: LaunchedSize: 10 mM × 1 mL, 50 mg, 100 mg
β-Caryophyllene ((-)-(E)-Caryophyllene; (−)-β-caryophyllene;
(−)-trans-Caryophyllene) Cat. No.: HY-N1415
β-Caryophyllene is a agonist.CB2 receptor
Purity: >95.0%Clinical Data: No Development ReportedSize: 500 mg
β-Cryptoxanthin ((3R)-β-Cryptoxanthin) Cat. No.: HY-108059
β-Cryptoxanthin ((3R)-β-Cryptoxanthin), isolatedfrom Satsuma mandarin orange, is an oxygenatedcarotenoid and a potent antioxidant.β-Cryptoxanthin has an anti-stress effect.
Purity: >98%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
β-Elemene ((-)-β-Elemene; Levo-β-elemene) Cat. No.: HY-107324
β-Elemene ((-)-β-Elemene; Levo-β-elemene) isisolated from natural plant Curcuma wenyujinwith an antitumor activity. β-Elemene can inducecell .apoptosis
Purity: 96.35%Clinical Data: Phase 3Size: 10 mM × 1 mL, 5 mg, 10 mg, 50 mg
β-Elemonic acidCat. No.: HY-N2454
β-Elemonic acid is a triterpene isolated from. β-Elemonic acid inducesBoswellia papyrifera
cell , reactive oxygen species ( ) andapoptosis ROS expression and inhibits .COX-2 prolyl endopeptidase
β-Elemonic acid exhibits anticancer andanti-inflammatory effects.
Purity: >99.0%Clinical Data: No Development ReportedSize: 5 mg, 10 mg, 20 mg
β-HederinCat. No.: HY-N7489
β-Hederin, a saponin isolated from Hedera helixL.(Araliaceae), possesses antileishmanialactivity. β-Hederin exhibits values of 1.5IC50
μM, 68 nM and 4.57 μM in L. Mexicanapromastigotes, amastigotes and THP1L. mexicanacells, respectively.
Purity: >97.0%Clinical Data: No Development ReportedSize: 1 mg, 5 mg
www.MedChemExpress.com 67