Chemistry:N'-Formylkynurenine
From HandWiki
| |
| Names | |
|---|---|
| Systematic IUPAC name
(2S)-2-Amino-4-(2-formamidophenyl)-4-oxobutanoic acid | |
| Other names
N′-Formyl-L-kynurenine
| |
| Identifiers | |
3D model (JSmol)
|
|
| MeSH | N'-formylkynurenine |
PubChem CID
|
|
| UNII | |
| |
| Properties | |
| C11H12N2O4 | |
| Molar mass | 236.227 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
| |
| Infobox references | |
N′-Formylkynurenine is an intermediate in the catabolism of tryptophan. It is a formylated derivative of kynurenine. The formation of N′-formylkynurenine is catalyzed by heme dioxygenases.[1]
See also
References
- ↑ Basran, Jaswir; Efimov, Igor; Chauhan, Nishma; Thackray, Sarah J; Krupa, James L; Eaton, Graham; Griffith, Gerry A; Mowat, Christopher G et al. (2011). "The Mechanism of Formation of N-Formylkynurenine by Heme Dioxygenases". Journal of the American Chemical Society 133 (40): 16251–16257. doi:10.1021/ja207066z. PMID 21892828.
 |  |
