Identification | Back Directory | [Name]
Hederagenin | [CAS]
465-99-6 | [Synonyms]
Hederidin NSC 24954 Rangefinder Hederogenin HEDERAGENIN hederagenol Hederagenine Kalosapogenin Vaccaric acid MELANTHIGENIN CAULOSAPOGENIN HEDERAGENIN(RG) astrantiagenine hederagenicacid Hederagenin, >=98% CAULOSAPOGENIN hplc Hederagenin 465-99-6 HEDERAGENIN WITH HPLC 3,23-Dihydroxyolean-12-en-28-acid 3,23-DIHYDROXYOLEAN-12-EN-28 OIC ACID 3-beta,23-dihydroxy-olean-12-en-28-oicaci (4R)-3β,23-Dihydroxyolean-12-en-28-oic acid (3b,4a)-3,23-Dihydroxyolean-12-en-28-oic acid (3β,4α) -3,23-Dihydroxy-olean-12-en- 28-oic acid Olean-12-en-28-oicacid, 3,23-dihydroxy-, (3b,4a)- Hederagenin, 98%, from Hedera nepalensisvar.sinensis (3-beta,4-alpha)-3,23-dihydroxyolean-12-en-28-oicacid 3,23-dihydroxy-,(3-beta,4-alpha)-olean-12-en-28-oicaci (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,12a-hexamethyl-9-methylol-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylicaci (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid | [EINECS(EC#)]
207-369-9 | [Molecular Formula]
C30H48O4 | [MDL Number]
MFCD00017385 | [MOL File]
465-99-6.mol | [Molecular Weight]
472.7 |
Chemical Properties | Back Directory | [Melting point ]
332-334° | [alpha ]
D20 +81° (c = 0.7 in pyridine) | [Boiling point ]
493.44°C (rough estimate) | [density ]
0.9871 (rough estimate) | [refractive index ]
1.4800 (estimate) | [storage temp. ]
2-8°C | [solubility ]
methanol: soluble1mg/mL | [form ]
Solid | [pka]
4.63±0.70(Predicted) | [color ]
White to Off-White | [λmax]
405nm(H2SO4)(lit.) | [Merck ]
14,4624 | [InChIKey]
PGOYMURMZNDHNS-MYPRUECHSA-N | [LogP]
7.410 (est) |
Hazard Information | Back Directory | [Description]
Hederagenin is a triterpene saponin that has been found in P. eximia with diverse biological activities.1,2,3,4,5 It increases production of reactive oxygen species (ROS), reduces colony formation, and induces apoptosis in cisplatin-resistant head and neck carcinoma (HNC) cells.2 In vivo, hederagenin (50, 100, and 200 mg/kg) suppresses tumor growth in a cisplatin-resistant HNC mouse xenograft model. It reduces aortic atherosclerotic lesion area, serum cholesterol and LDL levels, and inducible nitric oxide synthase (iNOS) protein levels in a rat model of atherosclerosis.3 Hederagenin (50 mg/kg) reduces ethanol-induced production of TNF-α, IL-6, and COX-2, alcohol dehydrogenase 2 (ALDH2) mRNA expression, and liver damage in a rat model of alcohol-induced hepatotoxicity.4 It also induces autophagy and inhibits oligomerization of α-synuclein in a mouse model of Parkinson''s disease induced by MPTP.5 | [Chemical Properties]
White Solid | [Uses]
Triterpenoid which can inhibit the proliferation of leukemia HL-60 cells. | [Definition]
ChEBI: A sapogenin that is olean-12-en-28-oic acid substituted by hydroxy groups at positions 3 and 23 (the 3beta stereoisomer). |
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