Vincaminol

Vincaminol
Names
	IUPAC name (3α,14β,16α)-14-(Hydroxymethyl)-14,15-dihydroeburnamenin-14-ol
	Systematic IUPAC name (3α,14β,16α)-14-(Hydroxymethyl)-14,15-dihydroeburnamenin-14-ol
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	174193;
PubChem CID	201188;
CompTox Dashboard (EPA)	DTXSID80955408 ;
	InChI InChI=1S/C20H26N2O2/c1-2-19-9-5-10-21-11-8-15-14-6-3-4-7-16(14)22(17(15)18(19)21)20(24,12-19)13-23/h3-4,6-7,18,23-24H,2,5,8-13H2,1H3/t18-,19+,20+/m1/s1 Key: YCXHPBHFOLIYEB-AABGKKOBSA-N; InChI=1/C20H26N2O2/c1-2-19-9-5-10-21-11-8-15-14-6-3-4-7-16(14)22(17(15)18(19)21)20(24,12-19)13-23/h3-4,6-7,18,23-24H,2,5,8-13H2,1H3/t18-,19+,20+/m1/s1 Key: YCXHPBHFOLIYEB-AABGKKOBBO;
	SMILES CC[C@@]12CCCN3[C@@H]1c4c(c5ccccc5n4[C@](C2)(CO)O)CC3;
Properties
Chemical formula	C20H26N2O2
Molar mass	326.440 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

Vincaminol (C₂₀H₂₆N₂O₂) is a chemical that is a part of the Vinca alkaloid group, which were discovered in the 1950s by a Canadian scientist and are derived from Vinca minor (periwinkle). Vincaminol is not as well known as some of the other Vinca alkaloids such as vinblastine, vinorelbine, vincristine, and vindesine, which are the four main, medically useful Vinca alkaloids.

Uses

Vincaminol is used in to synthesize vincamine.^{[citation needed]}

References

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