| Identification | Back Directory | [Name]
Desacetyl Vindoline | [CAS]
3633-92-9 | [Synonyms]
NSC 91993
Deacetylvindoline
Desacetyl Vindoline
4-Desacetylvindoline
(2β,3β,4β,5α,12R,19α)-6,7-Didehydro-3,4-dihydroxy-16-Methoxy-1-Methyl-aspidosperMidine-3-carboxylic Acid Methyl Ester
Aspidospermidine-3-carboxylic acid, 6,7-didehydro-3,4-dihydroxy-16-methoxy-1-methyl-, methyl ester, (2β,3β,4β,5α,12R,19α)-
(3aR,3a1R,4R,5S,5aR,10bR)-methyl 3a-ethyl-4,5-dihydroxy-8-methoxy-6-methyl-3a,3a1,4,5,5a,6,11,12-octahydro-1H-indolizino-[8,1-cd]carbazole-5-carboxylate | [Molecular Formula]
C23H30N2O5 | [MOL File]
3633-92-9.mol | [Molecular Weight]
414.49 |
| Chemical Properties | Back Directory | [Melting point ]
160-162°C | [storage temp. ]
Refrigerator | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
White to Off-White |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
Precursor to Vindoline during Vincristine biosynthesis. | [Definition]
ChEBI: 17-O-deacetylvindoline is a vinca alkaloid that is vindoline in which the acetate ester group at position 17 has been hydrolysed to give the corresponding secondary alcohol. It is a vinca alkaloid, an organic heteropentacyclic compound, a methyl ester, a tertiary alcohol and a secondary alcohol. It is functionally related to a vindoline. It is a conjugate base of a 17-O-deacetylvindolinium. |
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Carbosynth
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