For research use only. Not for therapeutic Use.
Epifriedelanol（Cat No.:R014236）is a pentacyclic triterpenoid alcohol widely distributed in medicinal plants. It has attracted attention for its diverse biological activities, including antioxidant, anti-inflammatory, anticancer, and antimicrobial effects. Research suggests that Epifriedelanol can suppress tumor growth, promote apoptosis, and modulate immune responses. It also exhibits wound-healing potential by supporting tissue repair and reducing oxidative stress. Its natural origin and pharmacological versatility make it a promising candidate for drug discovery and biomedical research, particularly in cancer, infectious diseases, and inflammatory disorders, as well as in traditional medicine applications.
| CAS Number | 16844-71-6 |
| Synonyms | (3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol |
| Molecular Formula | C30H52O |
| Purity | ≥95% |
| IUPAC Name | (3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol |
| InChI | InChI=1S/C30H52O/c1-20-21(31)9-10-22-27(20,5)12-11-23-28(22,6)16-18-30(8)24-19-25(2,3)13-14-26(24,4)15-17-29(23,30)7/h20-24,31H,9-19H2,1-8H3/t20-,21-,22+,23-,24+,26+,27+,28-,29+,30-/m0/s1 |
| InChIKey | XCDQFROEGGNAER-PFOIMGGJSA-N |
| SMILES | C[C@H]1[C@H](CC[C@@H]2[C@@]1(CC[C@H]3[C@]2(CC[C@@]4([C@@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C)C)C)C)C)O |
| Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |
