Hederagenin

Hederagenin
  • CAS No.:465-99-6
Other grades of this product :
Hederagenin Basic information
Product Name:Hederagenin
Synonyms:HEDERAGENIN(RG);(3β,4α) -3,23-Dihydroxy-olean-12-en- 28-oic acid;CAULOSAPOGENIN;HEDERAGENIN;3,23-DIHYDROXYOLEAN-12-EN-28 OIC ACID;(3-beta,4-alpha)-3,23-dihydroxyolean-12-en-28-oicacid;3,23-dihydroxy-,(3-beta,4-alpha)-olean-12-en-28-oicaci;3-beta,23-dihydroxy-olean-12-en-28-oicaci
CAS:465-99-6
MF:C30H48O4
MW:472.71
EINECS:207-369-9
Product Categories:Saponins;Pentacyclic Triterpenes;chemical reagent;pharmaceutical intermediate;phytochemical;Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Detergent
Mol File:465-99-6.mol
Hederagenin Chemical Properties
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. Sealed in dry,2-8°C
solubility methanol: soluble1mg/mL
pka4.63±0.70(Predicted)
form Solid
color White to Off-White
λmax405nm(H2SO4)(lit.)
Merck 14,4624
InChIKeyPGOYMURMZNDHNS-MYPRUECHSA-N
Safety Information
Hazard Codes Xi
Risk Statements 22
Safety Statements 22-45-24/25
WGK Germany 3
HS Code 29181990
MSDS Information
ProviderLanguage
Hederagenin English
Hederagenin Usage And Synthesis
DescriptionHederagenin is a triterpene saponin that has been found in P. eximia with diverse biological activities. It increases production of reactive oxygen species (ROS), reduces colony formation, and induces apoptosis in cisplatin-resistant head and neck carcinoma (HNC) cells. 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. 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. It also induces autophagy and inhibits oligomerization of α-synuclein in a mouse model of Parkinson''s disease induced by MPTP.
Chemical PropertiesWhite Solid
UsesTriterpenoid which can inhibit the proliferation of leukemia HL-60 cells.
DefinitionChEBI: A sapogenin that is olean-12-en-28-oic acid substituted by hydroxy groups at positions 3 and 23 (the 3beta stereoisomer).
Hederagenin Preparation Products And Raw materials

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