# Vindoline

> Mediated Wiki article. Canonical URL: https://mediated.wiki/source/Vindoline
> Markdown URL: https://mediated.wiki/source/Vindoline.md
> Source: https://en.wikipedia.org/wiki/Vindoline
> Source revision: 1282583237
> License: Creative Commons Attribution-ShareAlike 4.0 International (https://creativecommons.org/licenses/by-sa/4.0/)

{{Chembox
| ImageFile = Vindoline.svg
| ImageSize = 200px
| ImageAlt = 
| IUPACName = Methyl 3β,4β-dihydroxy-16-methoxy-1-methyl-6,7-didehydro-2β,5α,12β,19α-aspidospermidine-3α-carboxylate
| SystematicName = Methyl (3a''R'',3a<sup>1</sup>''R'',4''R'',5''S'',5a''R'',10b''R'')-4-(acetyloxy)-3a-ethyl-5-hydroxy-8-methoxy-6-methyl-3a,3a<sup>1</sup>,4,5,5a,6,11,12-octahydro-1''H''-indolizino[8,1-''cd'']carbazole-5-carboxylate
| OtherNames = 
|Section1={{Chembox Identifiers
| CASNo = 2182-14-1
| CASNo_Ref = {{cascite|correct|CAS}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 571PJ1LW03
| EINECS = 218-558-0
| PubChem = 260535
| ChemSpiderID = 228680
| SMILES = CC[C@@]12C=CCN3[C@@H]1[C@@]4(CC3)c5ccc(cc5N([C@H]4C([C@@H]2OC(=O)C)(C(=O)OC)O)C)OC
| InChI = 1/C25H32N2O6/c1-6-23-10-7-12-27-13-11-24(19(23)27)17-9-8-16(31-4)14-18(17)26(3)20(24)25(30,22(29)32-5)21(23)33-15(2)28/h7-10,14,19-21,30H,6,11-13H2,1-5H3/t19-,20+,21+,23+,24+,25-/m0/s1
| InChIKey = CXBGOBGJHGGWIE-ACSXSLCXBW
| StdInChI = 1S/C25H32N2O6/c1-6-23-10-7-12-27-13-11-24(19(23)27)17-9-8-16(31-4)14-18(17)26(3)20(24)25(30,22(29)32-5)21(23)33-15(2)28/h7-10,14,19-21,30H,6,11-13H2,1-5H3/t19-,20+,21+,23+,24+,25-/m0/s1
| StdInChIKey = CXBGOBGJHGGWIE-ACSXSLCXSA-N}}
|Section2={{Chembox Properties
| C=25 | H=32 | N=2 | O=6
| Appearance = 
| Density = 
| MeltingPt = 
| BoilingPt = 
| Solubility = }}
|Section3={{Chembox Hazards
| MainHazards = 
| FlashPt = 
| AutoignitionPt = }}
}}

'''Vindoline''' is a chemical precursor to [vinblastine](/source/vinblastine).<ref>{{cite journal |pmid= 23864440 |year= 2014 |last1= Liu |first1= J |title= Enhancement of vindoline and vinblastine production in suspension-cultured cells of Catharanthus roseus by artemisinic acid elicitation |journal= World Journal of Microbiology and Biotechnology |volume= 30 |issue= 1 |pages= 175–80 |last2= Zhu |first2= J |last3= Tang |first3= L |last4= Wen |first4= W |last5= Lv |first5= S |last6= Yu |first6= R |doi= 10.1007/s11274-013-1432-z |s2cid= 7350499 }}</ref>
Vindoline is formed through biosynthesis from [Tabersonine](/source/Tabersonine).

==See also==
* [Lochnericine](/source/Lochnericine)
* [Dimerization of catharanthine and vindoline](/source/Dimerization_of_catharanthine_and_vindoline)

==References==
{{reflist}}

{{Tryptamines}}

Category:Tryptamine alkaloids
Category:Indolizidines

{{alkaloid-stub}}

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Adapted from the Wikipedia article [Vindoline](https://en.wikipedia.org/wiki/Vindoline) by Wikipedia contributors ([contributor history](https://en.wikipedia.org/wiki/Vindoline?action=history)). Available under [Creative Commons Attribution-ShareAlike 4.0 International](https://creativecommons.org/licenses/by-sa/4.0/). Changes may have been made.