Gentianine
From Wikipedia, the free encyclopedia
| Names | |
|---|---|
| IUPAC name
5-Ethenyl-3,4-dihydropyrano[3,4-c]pyridin-1-one | |
| Other names
Erythricine | |
| Identifiers | |
3D model (JSmol) |
|
| 137011 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| KEGG | |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C10H9NO2 | |
| Molar mass | 175.187 g·mol−1 |
| Melting point | 82–83 °C (180–181 °F; 355–356 K)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Gentianine is a pyridine-derived alkaloid. Originally isolated in 1944 from Gentiana kirilowi,[2] it has also been found in Gentiana macrophylla,[3] fenugreek,[4] Strychnos angolensis,[5] Strychnos xantha,[5] and other plants.[1]
Gentianine is a crystalline solid with a melting point of 82-83 °C.[1] It is a base that forms salts, such as the hydrochloride salt, upon treatment with acids.[1]
Gentianine has been studied for its potential anti-inflammatory properties.[3][6][7][8]
