| Identification | Back Directory | [Name]
16-epi-isositsirikine | [CAS]
6519-27-3 | [Synonyms]
NSC 282700
NSC 338932
Rhazimanine
Isositsirikine
16-epi-isositsirikine
(16R)-E-Isositsirikine
(16R,19E)-19,20-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester
17,18-Secoyohimban-16-carboxylicacid,19,20-didehydro-17-hydroxy-,methylester
Indolo[2,3-a]quinolizine-2-acetic acid, 3-ethylidene-1,2,3,4,6,7,12,12b-octahydro-α-(hydroxymethyl)-, methyl ester, (αR,2R,3E,12bS)- | [Molecular Formula]
C21H26N2O3 | [MDL Number]
MFCD26406125 | [MOL File]
6519-27-3.mol | [Molecular Weight]
354.45 |
| Hazard Information | Back Directory | [Description]
An amorphous alkaloid found in Vinca rosea L., this laevorotatory base has
[α]25D - 20° (CHCI3). In EtOH, the ultraviolet spectrum has absorption maxima
at 224, 283 and 291 m/J.. The alkaloid forms a hemisulphate, m.p. 263.5°C and
an amorphous O-acetate. The picrate is obtained in the form of brilliant yellow
needles when crystallized from MeOH, m.p. 216°C. | [Uses]
(16R)-E-Isositsirikine is an indole alkaloid compound from Catharanthus roseus Tissue Cultures IV1[1]. | [Definition]
ChEBI: 16R,19E-isositsirikine is an alkaloid. It has a role as a metabolite. | [References]
Kutney, Brown., Tetrahedron, 22,321 (1966) |
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