cis-Homoaconitic acid
|
|
trans-Homoaconitic acid
|
|
Names | |
---|---|
IUPAC names
(1Z)-1-Butene-1,2,4-tricarboxylic acid
(1E)-1-Butene-1,2,4-tricarboxylic acid |
|
Other names
Homo-cis-aconitate; Homo-trans-aconitate
|
|
Identifiers | |
|
|
3D model (JSmol)
|
|
ChemSpider |
|
PubChem CID
|
|
|
|
Properties | |
C7H8O6 | |
Molar mass | 188.14 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 | |
Homoaconitatic acid (homoaconitate) is related to aconitic acid but with one extra carbon. It is part of the α-aminoadipate pathway for lysine biosynthesis, where it is made from homocitrate by homoaconitase. It is converted to homoisocitrate by homoisocitrate dehydrogenase.