Homoisocitric acid
Names | |
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IUPAC name
1-Hydroxy-1,2,4-butanetricarboxylic acid | |
Other names
3-Carboxy-2-hydroxyadipic acid | |
Identifiers | |
3562-75-2 | |
ChEBI | CHEBI:29094 |
ChemSpider | 4293958 |
Jmol 3D model | Interactive image |
KEGG | C05662 |
PubChem | 5119182 |
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Properties | |
C7H10O7 | |
Molar mass | 206.15 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 | |
Homoisocitric acid is an isomer of homocitric acid in which the hydroxyl is on the 2 position.[1] It is an intermediate in the α-aminoadipate pathway of lysine biosynthesis where it is produced by homocitrate synthase and is a substrate for homoaconitase.
Homoisocitrate is an anion, salt, or ester of homoisocitric acid.
See also
References
- ↑ "Homoisocitric Acid". U.S. National Library of Medicine; National Center for Biotechnology Information.
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