For research use only. Not for therapeutic Use.
16-Epivoacarpine(Cat No.:M134642)is an indole alkaloid belonging to the monoterpenoid indole alkaloid family, primarily isolated from plants of the Tabernaemontana genus. Structurally, it is a stereoisomer of voacarpine, differing at the C-16 position, which influences its biological activity. 16-Epivoacarpine has been studied for its antimalarial, anticancer, and antimicrobial properties, as well as potential neuroactive effects. Like related alkaloids, it interacts with key cellular pathways involved in apoptosis and pathogen defense. This rare natural product is significant in phytochemistry, pharmacology, and drug discovery exploring indole alkaloid–based therapeutics.
CAS Number | 114027-38-2 |
Synonyms | methyl (1R,12S,13R,14S,15E)-15-ethylidene-1-hydroxy-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate |
Molecular Formula | C21H24N2O4 |
Purity | ≥95% |
IUPAC Name | methyl (1R,12S,13R,14S,15E)-15-ethylidene-1-hydroxy-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraene-13-carboxylate |
InChI | InChI=1S/C21H24N2O4/c1-3-12-10-23-17-8-14-13-6-4-5-7-16(13)22-18(14)21(23,26)9-15(12)20(17,11-24)19(25)27-2/h3-7,15,17,22,24,26H,8-11H2,1-2H3/b12-3-/t15-,17-,20+,21+/m0/s1 |
InChIKey | ZROBSNVANUBAJZ-LWKNIGJSSA-N |
SMILES | C/C=C\1/CN2[C@H]3CC4=C([C@@]2(C[C@@H]1[C@@]3(CO)C(=O)OC)O)NC5=CC=CC=C45 |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |