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Hederagenin

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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
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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
pka
4.63±0.70(Predicted)
form 
Solid
color 
White to Off-White
λmax
405nm(H2SO4)(lit.)
Merck 
14,4624
InChIKey
PGOYMURMZNDHNS-MYPRUECHSA-N
LogP
7.410 (est)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
22
Safety Statements 
22-45-24/25
WGK Germany 
3
HS Code 
29181990

MSDS

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Hederagenin Usage And Synthesis

Description

Hederagenin 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 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).

HederageninSupplier

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