4-Hydroxyphenylpyruvic acid

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4-Hydroxyphenylpyruvic acid
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Names
IUPAC name
3-(4-hydroxyphenyl)-2-oxo-propanoic acid
Other names
4-Hydroxyphenylpyruvate
p-Hydroxyphenylpyruvic acid
p-Hydroxyphenylpyruvate
Identifiers
156-39-8 N
ChEBI CHEBI:15999 YesY
ChEMBL ChEMBL607712 YesY
ChemSpider 954 YesY
DrugBank DB07718 YesY
6629
Jmol 3D model Interactive image
KEGG C01179 YesY
PubChem 979
  • InChI=1S/C9H8O4/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,10H,5H2,(H,12,13) YesY
    Key: KKADPXVIOXHVKN-UHFFFAOYSA-N YesY
  • InChI=1/C9H8O4/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,10H,5H2,(H,12,13)
    Key: KKADPXVIOXHVKN-UHFFFAOYAH
  • O=C(O)C(=O)Cc1ccc(O)cc1
Properties
C9H8O4
Molar mass 180.157 g/mol
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

4-Hydroxyphenylpyruvic acid (4-HPPA) is an intermediate in the metabolism of the amino acid phenylalanine. The aromatic side chain of phenylalanine is hydroxylated by the enzyme phenylalanine hydroxylase to form tyrosine. The conversion from tyrosine to 4-HPPA is in turn catalyzed by tyrosine aminotransferase.[1] Additionally, 4-HPPA can be converted to homogentisic acid which is one of the precursors to ochronotic pigment.[2]

It is an intermediary compound in the biosynthesis of scytonemin.

See also

References

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