CAS 5092-09-1
:(3beta,16beta)-oleana-11,13(18)-diene-3,16,23,28-tetrol
Description:
The chemical substance known as "(3beta,16beta)-oleana-11,13(18)-diene-3,16,23,28-tetrol," with the CAS number 5092-09-1, is a type of triterpenoid, which is a class of chemical compounds derived from terpenes. Triterpenoids are characterized by their complex structures, typically consisting of 30 carbon atoms arranged in a specific configuration. This particular compound features multiple hydroxyl (-OH) groups, indicating it is a polyol, which contributes to its solubility in water and potential biological activity. The presence of diene functional groups suggests it may participate in various chemical reactions, including oxidation and polymerization. Triterpenoids are known for their diverse biological activities, including anti-inflammatory, antioxidant, and anticancer properties, making them of interest in pharmacological research. The specific stereochemistry of this compound, indicated by the beta configurations, plays a crucial role in its interaction with biological systems. Overall, this substance exemplifies the complexity and potential utility of natural products in medicinal chemistry.
Formula:C30H48O4
InChI:InChI=1/C30H48O4/c1-25(2)13-14-30(18-32)20(15-25)19-7-8-22-26(3)11-10-23(33)27(4,17-31)21(26)9-12-28(22,5)29(19,6)16-24(30)34/h7-8,21-24,31-34H,9-18H2,1-6H3/t21-,22-,23+,24+,26+,27+,28-,29-,30-/m1/s1
Synonyms:- (3beta,4alpha,16beta)-Oleana-11,13(18)-diene-3,16,23,28-tetrol
- Oleana-11,13(18)-Diene-3,16,23,28-Tetrol, (3Beta,16Beta)-
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Found 5 products.
Saikogenin A
CAS:<p>Saikogenin A is a dipeptidyl peptidase-4 inhibitor.</p>Formula:C30H48O4Purity:99.47%Color and Shape:SolidMolecular weight:472.7Saikogenin A
CAS:Controlled Product<p>Saikogenin A is a natural compound found in the tuberous roots of Pueraria lobata that has been shown to have a variety of biological activities. Saikogenin A inhibits protein synthesis through a number of mechanisms, including interfering with the production of growth factors, blocking the conversion of epoxyeicosatrienoic acids to prostaglandins, and inhibiting the activity of human liver cancer cells. It also has anti-inflammatory properties and has been shown to inhibit UV absorption as well as erythromycin-induced uvB damage in human skin cells. The triple-quadrupole mass spectrometry analysis reveals that saikogenin A has absorptions at 336, 338, and 340 nm in urine samples. This suggests that saikogenin A may be metabolized by cytochrome P450 enzymes into metabolites with different absorption spectra.</p>Formula:C30H48O4Purity:Min. 95%Molecular weight:472.7 g/mol




