Leukotriene A4
![]() | |
Names | |
---|---|
IUPAC name
4-{(2S,3S)-3-[(1E,3E,5Z,8Z)-1,3,5,8-Tetradecatetraen-1-yl]-2-oxiranyl}butanoic acid | |
Systematic IUPAC name
4-{(2S,3S)-3-[(1E,3E,5Z,8Z)-1,3,5,8-Tetradecatetraen-1-yl]-2-oxiranyl}butanoic acid | |
Identifiers | |
72059-45-1 ![]() | |
3D model (Jmol) | Interactive image |
ChEBI | CHEBI:15651 ![]() |
ChemSpider | 4444074 ![]() |
5214 | |
KEGG | C00909 ![]() |
MeSH | D017572 |
PubChem | 5280383 |
| |
| |
Properties | |
C20H30O3 | |
Molar mass | 318.450 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
![]() ![]() ![]() | |
Infobox references | |
Leukotriene A4 is a leukotriene. Leukotriene A4 hydrolase converts it to leukotriene B4. Leukotriene C4 synthase converts it to leukotriene C4.

Eicosanoid synthesis. (Leukotrienes at right.)
References
This article is issued from Wikipedia - version of the 11/30/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.