3-Ureidopropionic acid

From Wikipedia, the free encyclopedia
3-Ureidopropionic acid
Preferred IUPAC name

3-Ureidopropanoic acid[citation needed]

Systematic name

3-(Carbamoylamino)propanoic acid[1]

Identifiers
CAS number 462-88-4 YesY
PubChem 111
ChemSpider 109 YesY
KEGG C02642 YesY
MeSH N-carbamoyl-beta-alanine
ChEBI CHEBI:18261 YesY
ChEMBL CHEMBL20962 YesY
Beilstein Reference 1705263
Gmelin Reference 675230
3DMet B00472
Jmol-3D images {{#if:[nH2]:c(:[o]):[nH]CCc(:[o]):[oH]NC(=O)NCCC(O)=O|Image 1
Image 2
Properties
Molecular formula C4H8N2O3
Molar mass 132.12 g mol−1
Appearance White crystals
log P −1.23
Acidity (pKa) 4.408
Basicity (pKb) 9.589
Hazards
S-phrases S22, S24/25
Related compounds
Related alkanoic acids
Related compounds
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

3-Ureidopropionic acid is an intermediate in the metabolism of uracil. It is a urea derivative of beta-alanine.

References

  1. ↑ "N-carbamoyl-beta-alanine - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 16 September 2004. Identification. Retrieved 28 June 2012. 
Purine metabolism
Anabolism
R5P→IMP:
IMP→AMP:
IMP→GMP:
Catabolism
Pyrimidine metabolism
Anabolism
Catabolism
uracil:
thymine:

M: MET

mt, k, c/g/r/p/y/i, f/h/s/l/o/e, a/u, n, m

k, cgrp/y/i, f/h/s/l/o/e, au, n, m, epon

m (A16/C10), i (k, c/g/r/p/y/i, f/h/s/o/e, a/u, n, m)

  • Biochemical families: carbohydrates
    • alcohols
    • glycoproteins
    • glycosides
  • lipids
    • eicosanoids
    • fatty acids / intermediates
    • phospholipids
    • sphingolipids
    • steroids
  • nucleic acids
    • constituents / intermediates
  • proteins
    • Amino acids / intermediates
  • tetrapyrroles / intermediates
This article is issued from Wikipedia. The text is available under the Creative Commons Attribution/Share Alike; additional terms may apply for the media files.