For research use only. Not for therapeutic Use.
Alphitolic acid（Cat No.:M084576）is a naturally occurring pentacyclic triterpenoid derived from various plant sources. It belongs to the oleanane-type triterpenoids and exhibits potential pharmacological activities, including anti-inflammatory, anticancer, and antimicrobial effects. Its molecular structure features a hydroxyl and carboxyl functional group, contributing to its bioactivity and interactions with biological targets. Alphitolic acid is widely studied in natural product research, medicinal chemistry, and drug development, particularly for its role in modulating cellular pathways linked to oxidative stress, immune responses, and tumor suppression.
| CAS Number | 19533-92-7 |
| Synonyms | (1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aR,13bR)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid |
| Molecular Formula | C30H48O4 |
| Purity | ≥95% |
| IUPAC Name | (1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aR,13bR)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid |
| InChI | InChI=1S/C30H48O4/c1-17(2)18-10-13-30(25(33)34)15-14-28(6)19(23(18)30)8-9-22-27(5)16-20(31)24(32)26(3,4)21(27)11-12-29(22,28)7/h18-24,31-32H,1,8-16H2,2-7H3,(H,33,34)/t18-,19+,20+,21-,22+,23+,24-,27-,28+,29+,30-/m0/s1 |
| InChIKey | PFCVZKFJHRCLCC-PGOIBATFSA-N |
| SMILES | CC(=C)[C@@H]1CC[C@]2([C@H]1[C@H]3CC[C@H]4[C@]([C@@]3(CC2)C)(CC[C@@H]5[C@@]4(C[C@H]([C@@H](C5(C)C)O)O)C)C)C(=O)O |
| Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |
