For research use only. Not for therapeutic Use.
20(S),24(R)-Ocotillol（Cat No.:R072347）is a dammarane-type triterpenoid saponin derivative, structurally related to ginsenosides found in Panax species. It is recognized for its diverse pharmacological properties, including cardioprotective, neuroprotective, and anti-inflammatory effects. Research indicates that 20(S),24(R)-Ocotillol can modulate cellular stress responses, reduce oxidative damage, and improve mitochondrial function, making it valuable in studies on cardiovascular and neurological disorders. Additionally, it shows antitumor potential by regulating apoptosis and cell cycle pathways. With its unique stereochemistry and bioactivity, this compound remains a promising candidate in natural product and therapeutic research.
| CAS Number | 69926-31-4 |
| Synonyms | (3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6,12-triol |
| Molecular Formula | C30H52O5 |
| Purity | ≥95% |
| IUPAC Name | (3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6,12-triol |
| InChI | InChI=1S/C30H52O5/c1-25(2)21(33)10-12-27(5)20-15-18(31)23-17(30(8)14-11-22(35-30)26(3,4)34)9-13-28(23,6)29(20,7)16-19(32)24(25)27/h17-24,31-34H,9-16H2,1-8H3/t17-,18+,19-,20+,21-,22+,23-,24-,27+,28+,29+,30-/m0/s1 |
| InChIKey | XIGBHUXQOPWGDK-HTGHARJWSA-N |
| SMILES | C[C@]1(CC[C@@H](O1)C(C)(C)O)[C@H]2CC[C@@]3([C@@H]2[C@@H](C[C@H]4[C@]3(C[C@@H]([C@@H]5[C@@]4(CC[C@@H](C5(C)C)O)C)O)C)O)C |
| Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |
