Vincaminol

Vincaminol
Names
	IUPAC name 14α-(Hydroxymethyl)-14,15-dihydro-3α,16α-eburnamenin-14β-ol
	Systematic 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 ;
3D model (JSmol)	Interactive image;
ChemSpider	174193;
PubChem CID	201188;
UNII	S4D53C4NN7 ;
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).^[1]^[2] 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

^ PubChem. "Vincaminol". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-11-15.
^ Smeyers, Yves G.; Smeyers, Nadine J.; Randez, Juan J.; Hernandez-Laguna, A.; Galvez-Ruano, E. (1991-06-01). "A structural and pharmacological study of alkaloids of Vinca Minor". Molecular Engineering. 1 (2): 153–160. doi:10.1007/BF00420051. ISSN 1572-8951. S2CID 93210480.

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

[1] PubChem. "Vincaminol". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-11-15.

[2] Smeyers, Yves G.; Smeyers, Nadine J.; Randez, Juan J.; Hernandez-Laguna, A.; Galvez-Ruano, E. (1991-06-01). "A structural and pharmacological study of alkaloids of Vinca Minor". Molecular Engineering. 1 (2): 153–160. doi:10.1007/BF00420051. ISSN 1572-8951. S2CID 93210480.

[1]

[2]

Names

IUPAC name 14α-(Hydroxymethyl)-14,15-dihydro-3α,16α-eburnamenin-14β-ol
Systematic 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
UNII	S4D53C4NN7^Y
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