Chemistry:Vindoline
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(Redirected from Chemistry:C25H32N2O6)
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Names | |
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IUPAC name
Methyl 3β,4β-dihydroxy-16-methoxy-1-methyl-6,7-didehydro-2β,5α,12β,19α-aspidospermidine-3α-carboxylate
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Systematic IUPAC name
Methyl (3aR,3a1R,4R,5S,5aR,10bR)-4-(acetyloxy)-3a-ethyl-5-hydroxy-8-methoxy-6-methyl-3a,3a1,4,5,5a,6,11,12-octahydro-1H-indolizino[8,1-cd]carbazole-5-carboxylate | |
Identifiers | |
3D model (JSmol)
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EC Number |
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PubChem CID
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Properties | |
C25H32N2O6 | |
Molar mass | 456.539 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Tracking categories (test):
Vindoline is a chemical precursor to vinblastine.[1] Vindoline is formed through biosynthesis from Tabersonine.
See also
References
- ↑ Liu, J; Zhu, J; Tang, L; Wen, W; Lv, S; Yu, R (2014). "Enhancement of vindoline and vinblastine production in suspension-cultured cells of Catharanthus roseus by artemisinic acid elicitation". World Journal of Microbiology and Biotechnology 30 (1): 175–80. doi:10.1007/s11274-013-1432-z. PMID 23864440.
![]() | Original source: https://en.wikipedia.org/wiki/Vindoline.
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