Homoisocitric acid

{{Chembox

| ImageFile = Homoisocitric acid.svg

| ImageSize = 200px

| PIN = 1-Hydroxybutane-1,2,4-tricarboxylic acid

| OtherNames = 3-Carboxy-2-hydroxyadipic acid

|Section1={{Chembox Identifiers

| CASNo = 3562-75-2

| PubChem = 5119182

| ChemSpiderID = 4293958

| ChEBI=29094

| KEGG=C05662

| SMILES = O=C(O)CCC(C(=O)O)C(O)C(=O)O

| InChI = 1/C7H10O7/c8-4(9)2-1-3(6(11)12)5(10)7(13)14/h3,5,10H,1-2H2,(H,8,9)(H,11,12)(H,13,14)

| InChIKey = OEJZZCGRGVFWHK-UHFFFAOYAM

| StdInChI = 1S/C7H10O7/c8-4(9)2-1-3(6(11)12)5(10)7(13)14/h3,5,10H,1-2H2,(H,8,9)(H,11,12)(H,13,14)

| StdInChIKey = OEJZZCGRGVFWHK-UHFFFAOYSA-N

}}

|Section2={{Chembox Properties

| C=7 | H=10 | O=7

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|Section3={{Chembox Hazards

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Homoisocitric acid is an isomer of homocitric acid in which the hydroxyl is on the 2 position. {{Cite web | title=Homoisocitric Acid| url=https://pubchem.ncbi.nlm.nih.gov/compound/5119182|publisher=U.S. National Library of Medicine; National Center for Biotechnology Information}} 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