From Wikipedia, the free encyclopedia
Vinorine
|
Names
|
Other names
22-Norajmala-1,19-dien-17α-yl acetate
|
Identifiers
|
|
|
|
|
ChEBI
|
|
KEGG
|
|
|
|
InChI=1S/C21H22N2O2/c1-3-12-10-23-16-8-13(12)18-17(23)9-21(20(18)25-11(2)24)14-6-4-5-7-15(14)22-19(16)21/h3-7,13,16-18,20H,8-10H2,1-2H3/b12-3-/t13-,16-,17-,18?,20+,21+/m0/s1 Key: CLDVMRAEPFQOSD-WEOXKLFPSA-N
|
C/C=C\1/CN2[C@H]3C[C@@H]1C4[C@@H]2C[C@]5([C@@H]4OC(=O)C)C3=NC6=CC=CC=C56
|
Properties
|
|
C21H22N2O2
|
Molar mass
|
334.419 g·mol−1
|
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Chemical compound
Vinorine is an
indole alkaloid isolated from
Alstonia.
[2]
References
-
^ Chambers, Michael.
"ChemIDplus - 0034020070 - CLDVMRAEPFQOSD-SZBATKQJSA-N - Vinorine - Similar structures search, synonyms, formulas, resource links, and other chemical information". chem.nlm.nih.gov.
-
^ Cao, P.; Liang, Y.; Gao, X.; Li, X. M.; Song, Z. Q.; Liang, G. (2012).
"Monoterpenoid indole alkaloids from Alstonia yunnanensis and their cytotoxic and anti-inflammatory activities". Molecules (Basel, Switzerland). 17 (11): 13631–41.
doi:
10.3390/molecules171113631.
PMC
6268798.
PMID
23159924.