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H3916

Sigma-Aldrich

Hederagenin

≥97% (HPLC)

Synonyme(s) :

3,23-Dihydroxyolean-12-en-28-acid, Astrantiagenin E, Caulosapogenin, Hederagenic acid, Hederagenol

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About This Item

Formule empirique (notation de Hill):
C30H48O4
Numéro CAS:
465-99-6
Poids moléculaire :
472.70
Numéro MDL:
MFCD00017385
Code UNSPSC :
41116107
Nomenclature NACRES :
NA.25

Pureté

≥97% (HPLC)

Solubilité

methanol: 1 mg/mL

Température de stockage

2-8°C

Chaîne SMILES 

O[C@H]1CC[C@@]2(C)[C@](CC[C@]3(C)[C@]2([H])CC=C4[C@@]3(C)CC[C@]5(C(O)=O)[C@@]4([H])CC(C)(C)CC5)([H])[C@]1(C)CO

InChI

1S/C30H48O4/c1-25(2)13-15-30(24(33)34)16-14-28(5)19(20(30)17-25)7-8-22-26(3)11-10-23(32)27(4,18-31)21(26)9-12-29(22,28)6/h7,20-23,31-32H,8-18H2,1-6H3,(H,33,34)/t20-,21+,22+,23-,26-,27-,28+,29+,30-/m0/s1

Clé InChI

PGOYMURMZNDHNS-MYPRUECHSA-N

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Application

Hederagenin (3,23-Dihydroxyolean-12-en-28-acid), a triterpenoid saponin, is used to study the properties of triterpenoid saponins as biopesticides that prevent fungal growth, bacterial growth, and viral plant diseases. Hederagenin may be used as a reference in assays to detect it in biological fluids.

Actions biochimiques/physiologiques

Saponin. Anti-inflammatory.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Oleanolic acid United States Pharmacopeia (USP) Reference Standard

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00930585

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β-Amyrin analytical standard

Supelco

09236

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He Zhu et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(30), 3407-3414 (2011-10-04)
A new liquid chromatography-tandem mass spectrometry (LC-MS/MS) method operated in the positive/negative electrospray ionization (ESI) switching mode has been developed and validated for the simultaneous determination of asperosaponin VI and its active metabolite hederagenin in rat plasma. After addition of
Xuemei Yang et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 879(21), 1973-1979 (2011-06-18)
A rapid, sensitive and selective method was developed for the quantitative determination of hederagenin in rat plasma and cerebrospinal fluid (CSF) by ultra fast liquid chromatography-tandem mass spectrometry (UFLC-MS/MS). It has been successfully applied in a pharmacokinetic study of hederagenin
Qiongming Xu et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 34(20), 2610-2612 (2010-01-15)
To investigate the chemical constituents from roots of Boehmeria nivea. The constituents were isolated by repeated column chromatography and preparative liquid chromatography; and their structures were elucidated by chemical properties and spectroscopic analyses. Seven compounds were isolated and their structures
Zeng-Liang Jin et al.
Pharmacology, biochemistry, and behavior, 100(3), 431-439 (2011-10-19)
Fructus Akebiae is a traditional Chinese herbal extract that has been used for the treatment of depressive disorders in China. Previous studies demonstrated that Fructus Akebiae extracts (FAE) displayed a potent antidepressant-like activity in animal behavior tests and found that
Massimo Confalonieri et al.
Plant biotechnology journal, 7(2), 172-182 (2008-12-06)
Triterpene saponins are a group of bioactive compounds abundant in the genus Medicago, and have been studied extensively for their biological and pharmacological properties. In this article, we evaluated the effects of the ectopic expression of AsOXA1 cDNA from Aster
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