Chemistry:Homoisocitric acid
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Revision as of 01:12, 28 November 2020 by imported>QCDvac (add)
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Names | |
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Preferred IUPAC name
1-Hydroxybutane-1,2,4-tricarboxylic acid | |
Other names
3-Carboxy-2-hydroxyadipic acid
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
KEGG | |
PubChem CID
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Properties | |
C7H10O7 | |
Molar mass | 206.150 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 | |
Tracking categories (test):
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. https://pubchem.ncbi.nlm.nih.gov/compound/5119182.
![]() | Original source: https://en.wikipedia.org/wiki/Homoisocitric acid.
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