4-Hydroxy-2-oxopentanoaic acid, also known as 4-hydroxy-2-oxovalerate, is formed by the decarboxylation of 4-oxalocrotonate by 4-oxalocrotonate decarboxylase, is degraded by 4-hydroxy-2-oxovalerate aldolase, forming acetaldehyde and pyruvate and is reversibly dehydrated by 2-oxopent-4-enoate hydratase to 2-oxopent-4-enoate.[1]
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Preferred IUPAC name
4-Hydroxy-2-oxopentanoic acid | |
Other names
4-Hydroxy-2-ketopentanoic acid; 4-Hydroxy-2-ketovaleric acid; 4-Hydroxy-2-oxovaleric acid; 4-Hydroxy-2-oxopentanoate; 4-Hydroxy-2-ketopentanoate; 4-Hydroxy-2-ketovalerate; 4-Hydroxy-2-oxovalerate; HKP
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3D model (JSmol)
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C5H8O4 | |
Molar mass | 132.115 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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References
edit- ^ Kunz DA, Ribbons DW, Chapman PJ (1981). "Metabolism of allylglycine and cis-crotylglycine by Pseudomonas putida (arvilla) mt-2 harboring a TOL plasmid". J. Bacteriol. 148 (1): 72–82. doi:10.1128/JB.148.1.72-82.1981. PMC 216168. PMID 7287632.
External links
edit- 4-Hydroxy-2-ketovalerate, biocyc.org