Vincoline

Vincoline
Names
	IUPAC name Methyl (2β,3β,5α,12β,19α,20S)-2-hydroxy-6,7-didehydro-3,20-epoxyaspidospermidine-3-carboxylate
Identifiers
CAS Number	11034-66-5;
3D model (JSmol)	Interactive image;
ChemSpider	2297507;
PubChem CID	3032566;
CompTox Dashboard (EPA)	DTXSID60911603 ;
	InChI InChI=1S/C21H24N2O4/c1-13-18-8-5-10-23-11-9-19(16(18)23)14-6-3-4-7-15(14)22-21(19,25)20(12-18,27-13)17(24)26-2/h3-8,13,16,22,25H,9-12H2,1-2H3/t13-,16-,18-,19+,20-,21-/m0/s1 Key: YOQNZWXFGROKGY-KVKBDHCBSA-N; InChI=1/C21H24N2O4/c1-13-18-8-5-10-23-11-9-19(16(18)23)14-6-3-4-7-15(14)22-21(19,25)20(12-18,27-13)17(24)26-2/h3-8,13,16,22,25H,9-12H2,1-2H3/t13-,16-,18-,19+,20-,21-/m0/s1 Key: YOQNZWXFGROKGY-KVKBDHCBBE;
	SMILES C[C@H]1[C@]23C[C@@](O1)([C@]4([C@@]5([C@H]2N(CC5)CC=C3)c6ccccc6N4)O)C(=O)OC;
Properties
Chemical formula	C21H24N2O4
Molar mass	368.426
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Vincoline is an alkaloid isolated from Catharanthus roseus.[1] In a mouse model, it has been found to stimulate insulin secretion.[2]

References

Aynilian, GH; Weiss, SG; Cordell, GA; Abraham, DJ; Crane, FA; Farnsworth, NR (1974). "Catharanthus alkaloids. XXIX. Isolation and structure elucidation of vincoline". Journal of Pharmaceutical Sciences. 63 (4): 536–8. doi:10.1002/jps.2600630409. PMID 4828700.
Yao, XG; Chen, F; Li, P; Quan, L; Chen, J; Yu, L; Ding, H; Li, C; Chen, L; Gao, Z; Wan, P; Hu, L; Jiang, H; Shen, X (2013). "Natural product vindoline stimulates insulin secretion and efficiently ameliorates glucose homeostasis in diabetic murine models". Journal of Ethnopharmacology. 150 (1): 285–97. doi:10.1016/j.jep.2013.08.043. PMID 24012527.

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