beta-Ureidoisobutyric acid

Beta-Ureidoisobutyric acid
Names

Preferred IUPAC name 2-Methyl-3-ureidopropanoic acid
Systematic IUPAC name 3-(Carbamoylamino)-2-methylpropanoic acid^[1]
Identifiers
CAS Number	2905-86-4^N
3DMet	B00750
Beilstein Reference	1768736
ChEBI	CHEBI:1670^Y
ChemSpider	141172^Y
Jmol interactive 3D	Image Image
KEGG	C05100^N
MeSH	beta-ureidoisobutyric+acid
PubChem	[https://pubchem.ncbi.nlm.nih.gov/compound/160663 Template:Puchemcite 160663 Template:Puchemcite] 55289370 R
InChI InChI=1S/C5H10N2O3/c1-3(4(8)9)2-7-5(6)10/h3H,2H2,1H3,(H,8,9)(H3,6,7,10)^Y Key: PHENTZNALBMCQD-UHFFFAOYSA-N^Y
SMILES CC(C[nH]:c(:[nH2]):[o])c(:[o]):[oH] CC(CNC(N)=O)C(O)=O
Properties
Chemical formula	C₅H₁₀N₂O₃
Molar mass	146.15 g·mol⁻¹
Related compounds
Related alkanoic acids	3-Ureidopropionic acid Carbamoyl aspartic acid N-Acetylaspartic acid
Related compounds	Biuret Bromisoval Carbromal
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

β-Ureidoisobutyric acid is an intermediate in the catabolism of thymine.

References

↑ "beta-ureidoisobutyric acid - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 16 September 2004. Identification. Retrieved 28 June 2012.

Nucleotide metabolic intermediates

Purine metabolism

Anabolism

R5P→IMP:	R5P PRPP PRA GAR FGAR FGAM AIR CAIR SAICAR AICAR FAICAR

IMP→AMP:	Adenylosuccinate

IMP→GMP:	Xanthosine monophosphate

Catabolism

Pyrimidine metabolism

Anabolism

Catabolism

uracil:	Dihydrouracil 3-Ureidopropionic acid β-Alanine

thymine:	Dihydrothymine β-Ureidoisobutyric acid 3-Aminoisobutyric acid

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