Carbamoyl aspartic acid

Carbamoyl aspartic acid
Skeletal formula of carbamoyl aspartic acid
Names
IUPAC name
2-(Carbamoylamino)butanedioic acid[1]
Identifiers
CAS Number
  • 923-37-5 checkY
  • 13184-27-5 S checkY
3D model (JSmol)
  • Interactive image
3DMet
  • B00115
Beilstein Reference
 1726861, 1726860 S
ChEBI
  • CHEBI:15859 checkY
ChEMBL
  • ChEMBL1161506 checkY
ChemSpider
  • 273 checkY
  • 1267120 R checkY
  • 84022 S checkY
DrugBank
  • DB04252 checkY
ECHA InfoCard 100.011.906 Edit this at Wikidata
EC Number
  • 213-096-6
KEGG
  • C00438 checkY
MeSH ureidosuccinic+acid
PubChem CID
  • 279
  • 1550569 R
  • 93072 S
UNII
  • O3Y2KY16L1 checkY
  • R2521024DK S checkY
CompTox Dashboard (EPA)
  • DTXSID701030182 Edit this at Wikidata
InChI
  • InChI=1S/C5H8N2O5/c6-5(12)7-2(4(10)11)1-3(8)9/h2H,1H2,(H,8,9)(H,10,11)(H3,6,7,12) checkY
    Key: HLKXYZVTANABHZ-UHFFFAOYSA-N checkY
  • NC(=O)NC(CC(=O)O)C(=O)O
Properties
Chemical formula
 C5H8N2O5
Molar mass 176.128 g·mol−1
log P −0.663
Acidity (pKa) 3.649
Basicity (pKb) 10.348
Related compounds
Related alkanoic acids
  • 3-Ureidopropionic acid
  • beta-Ureidoisobutyric acid
  • N-Acetylaspartic acid
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Carbamoyl aspartic acid (or ureidosuccinic acid) is a carbamate derivative, serving as an intermediate in pyrimidine biosynthesis.

References

  1. ^ "ureidosuccinic acid - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification. Retrieved 27 June 2012.
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purine
metabolism
anabolism
R5P→IMP:
IMP→AMP:
IMP→GMP:
catabolism
pyrimidine
metabolism
anabolism
catabolism
uracil:
thymine:
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