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3-Hydroxyisobutyric acid

From Wikipedia, the free encyclopedia
3-Hydroxyisobutyric acid
Names
Preferred IUPAC name
3-Hydroxy-2-methylpropanoic acid
Other names
3-Hydroxyisobutyric acid
Identifiers
3D model (JSmol)
1745484
ChEBI
ChemSpider
ECHA InfoCard100.254.271Edit this at Wikidata
EC Number
  • 819-819-7
KEGG
UNII
  • InChI=1S/C4H8O3/c1-3(2-5)4(6)7/h3,5H,2H2,1H3,(H,6,7) checkY
    Key: DBXBTMSZEOQQDU-UHFFFAOYSA-N checkY
  • InChI=1/C4H8O3/c1-3(2-5)4(6)7/h3,5H,2H2,1H3,(H,6,7)
    Key: DBXBTMSZEOQQDU-UHFFFAOYAC
  • OC(C(C)CO)=O
  • O=C(O)C(C)CO
Properties
C4H8O3
Molar mass104.10 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

3-Hydroxyisobutyric acid (or3-hydroxy-2-methylpropanoic acid)[1] is an intermediate in the metabolism ofvaline.[2] It is achiral compound having twoenantiomers,D-3-hydroxyisobutyric acid andL-3-hydroxyisobutyric acid.

See also

[edit]

References

[edit]
  1. ^PubChem."3-Hydroxyisobutyric acid".pubchem.ncbi.nlm.nih.gov. Retrieved2022-11-24.
  2. ^"Human Metabolome Database: Showing metabocard for (S)-3-Hydroxyisobutyric acid (HMDB0000023)".hmdb.ca. Retrieved2022-11-24.
Kacetyl-CoA
lysine
leucine
tryptophanalanine
G
G→pyruvate
citrate
glycine
serine
G→glutamate
α-ketoglutarate
histidine
proline
arginine
other
G→propionyl-CoA
succinyl-CoA
valine
isoleucine
methionine
threonine
propionyl-CoA
G→fumarate
phenylalaninetyrosine
G→oxaloacetate
Other
Cysteine metabolism

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