Chemistry:Vindoline

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Vindoline
Vindoline.svg
Names
IUPAC name
Methyl 3β,4β-dihydroxy-16-methoxy-1-methyl-6,7-didehydro-2β,5α,12β,19α-aspidospermidine-3α-carboxylate
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)
ChemSpider
EC Number
  • 218-558-0
UNII
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).
Infobox references
Tracking categories (test):

Vindoline is a chemical precursor to vinblastine.[1] Vindoline is formed through biosynthesis from Tabersonine.

See also

References

  1. 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.