Echinocystic acid

• CAT Number: I003826
• CAS Number: 510-30-5
• Molecular Formula: C30H48O4
• Molecular Weight: 472.7
• Purity: ≥95%
• Storage: Store at -20°C
• IUPAC Name: (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
• InChI: InChI=1S/C30H48O4/c1-25(2)14-15-30(24(33)34)19(16-25)18-8-9-21-27(5)12-11-22(31)26(3,4)20(27)10-13-28(21,6)29(18,7)17-23(30)32/h8,19-23,31-32H,9-17H2,1-7H3,(H,33,34)/t19-,20-,21+,22-,23+,27-,28+,29+,30+/m0/s1
• InChIKey: YKOPWPOFWMYZJZ-PRIAQAIDSA-N
• SMILES: CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C(=O)O)C

Echinocystic acid (Cat.No:I003826) is a naturally occurring triterpenoid compound found in various medicinal plants. It possesses diverse pharmacological activities, including anti-inflammatory, antioxidant, and anticancer properties. Echinocystic acid shows potential in the treatment of conditions such as inflammation, cancer, diabetes, and cardiovascular diseases. Further research is ongoing to explore its therapeutic applications.

Reference

[1]. Yang JH et al. Echinocystic acid inhibits RANKL-induced osteoclastogenesis by regulating NF-κB and ERK signaling pathways. Biochem Biophys Res Commun. 2016 Sep 2;477(4):673-7.

[2]. Ma Z et al. Echinocystic Acid Inhibits IL-1β-Induced COX-2 and iNOS Expression in Human Osteoarthritis Chondrocytes. Inflammation. 2016 Apr;39(2):543-9.

[3]. Li S et al. Echinocystic acid reduces reserpine-induced pain/depression dyad in mice. Metab Brain Dis. 2016 Apr;31(2):455-63.