CAS 201534-09-0
:(3α,20α,22α)-3,22-Dihydroxyolean-12-en-29-oic acid
Description:
(3α,20α,22α)-3,22-Dihydroxyolean-12-en-29-oic acid, commonly known as oleanolic acid, is a pentacyclic triterpenoid compound that exhibits a variety of biological activities. It is characterized by its oleanane skeleton, which consists of five interconnected rings. The presence of hydroxyl groups at the 3α and 22α positions contributes to its solubility and reactivity, while the carboxylic acid group at the 29 position enhances its potential for biological interactions. Oleanolic acid is known for its anti-inflammatory, antioxidant, and hepatoprotective properties, making it of interest in pharmacological research. It is found in various plants, particularly in the leaves and fruits of olive trees and other medicinal herbs. The compound has been studied for its potential therapeutic effects, including its role in metabolic regulation and its ability to modulate cellular signaling pathways. Its safety profile and low toxicity further support its potential use in dietary supplements and natural health products.
Formula:C30H48O4
InChI:InChI=1S/C30H48O4/c1-25(2)20-10-13-30(7)21(28(20,5)12-11-22(25)31)9-8-18-19-16-26(3,24(33)34)17-23(32)27(19,4)14-15-29(18,30)6/h8,19-23,31-32H,9-17H2,1-7H3,(H,33,34)/t19-,20-,21+,22+,23-,26-,27+,28-,29+,30+/m0/s1
InChI key:InChIKey=JTBGJQZJEYVBJZ-SXKKXCELSA-N
SMILES:C[C@]12[C@@]([C@]3(C)[C@@](CC1)(C(C)(C)[C@H](O)CC3)[H])(CC=C4[C@@]2(C)CC[C@]5(C)[C@]4(C[C@@](C(O)=O)(C)C[C@@H]5O)[H])[H]
Synonyms:- Triptocallic acid D
- (3α,20α,22α)-3,22-Dihydroxyolean-12-en-29-oic acid
- Olean-12-en-29-oic acid, 3,22-dihydroxy-, (3α,20α,22α)-
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Found 3 products.
Triptocallic acid D
CAS:<p>Triptocallic acid D is a natural product for research related to life sciences. The catalog number is TN5182 and the CAS number is 201534-09-0.</p>Formula:C30H48O4Purity:98%Color and Shape:SolidMolecular weight:472.7Triptocallic acid D
CAS:Controlled Product<p>Triptocallic acid D is a naturally occurring fungal metabolite, which is derived from specific fungal species. It exhibits its mode of action through the inhibition of key biological pathways, potentially disrupting cellular processes associated with pathogenic organisms. This compound has garnered interest in scientific research due to its bioactive properties.</p>Formula:C30H48O4Purity:Min. 95%Molecular weight:472.7 g/mol


