Vincaminol

Names
IUPAC name (3α,14β,16α)-14-(Hydroxymethyl)-14,15-dihydroeburnamenin-14-ol
Preferred IUPAC name (41S,12S,13aS)-13a-Ethyl-12-(hydroxymethyl)-2,3,41,5,6,12,13,13a-octahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridin-12-ol
Identifiers
CAS Number	3382-95-4 Y
3D model (JSmol)	Interactive image
ChemSpider	174193
PubChem CID	201188
CompTox Dashboard (EPA)	DTXSID80955408
show 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
show 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[]

This article does not cite any sources. Please help by adding citations to reliable sources. Unsourced material may be challenged and removed. Find sources:  –  ·  ·  · scholar · JSTOR (December 2014) (Learn how and when to remove this template message)

This article about an alkaloid is a stub. You can help Wikipedia by .

• v
• t