Terpene

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2-Oxoadipic acid[1]
Skeletal formula of α-ketoadipic acid
Skeletal formula of α-ketoadipic acid
Ball and stick model of α-ketoadipic acid
Ball and stick model of α-ketoadipic acid
Names
Preferred IUPAC name
2-Oxohexanedioic acid[2]
Other names
α-Ketoadipic acid
2-Ketoadipic acid
α-Oxoadipic acid
Identifiers
3D model (JSmol)
3DMet
ChEBI
ChemSpider
ECHA InfoCard 100.164.320 Edit this at Wikidata
KEGG
MeSH Alpha-ketoadipic+acid
UNII
  • InChI=1S/C6H8O5/c7-4(6(10)11)2-1-3-5(8)9/h1-3H2,(H,8,9)(H,10,11) checkY
    Key: FGSBNBBHOZHUBO-UHFFFAOYSA-N checkY
  • InChI=1/C6H8O5/c7-4(6(10)11)2-1-3-5(8)9/h1-3H2,(H,8,9)(H,10,11)
    Key: FGSBNBBHOZHUBO-UHFFFAOYAU
  • C(CC(=O)C(=O)O)CC(=O)O
  • O=C(C(=O)O)CCCC(=O)O
Properties
C6H8O5
Molar mass 160.125 g·mol−1
Density 1.4 g cm−3
Melting point 125 °C (257 °F; 398 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

2-Oxoadipic acid, also known as α-ketoadipic acid, is an intermediate in the metabolism of lysine and tryptophan.[3][4] The conjugate base and carboxylate is 2-oxoadipate or α-ketoadipate, which is the biochemically relevant form.

See also[edit]

References[edit]

  1. ^ 2-oxoadipate - Compound Summary, PubChem.
  2. ^ "Alpha-ketoadipic acid". The PubChem Project. National Center for Biotechnology Information.
  3. ^ Voet, Donald; Voet, Judith G. (2011). Biochemistry (4th ed.). Hoboken, NJ: Wiley. pp. 1040–1043. ISBN 978-0-470-57095-1.
  4. ^ Dobrota, Dušan (2016). Lekárska biochémia [Medical biochemistry] (in Slovak) (2nd ed.). Martin: Osveta. pp. 329–330, 335–337. ISBN 978-80-8063-444-5.


source: https://en.wikipedia.org/wiki/Alpha-Ketoadipic_acid

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