Carbamoyl aspartic acid

Carbamoyl aspartic acid
Names

IUPAC name 2-(Carbamoylamino)butanedioic acid^[1]
Identifiers
CAS Number	923-37-5^Y 13184-27-5 S^Y
3D model (Jmol)	Interactive image Interactive image
3DMet	B00115
Beilstein Reference	1726861, 1726860 S
ChEBI	CHEBI:15859^Y
ChEMBL	ChEMBL1161506^Y
ChemSpider	273^Y 1267120 R^Y 84022 S^Y
DrugBank	DB04252^Y
ECHA InfoCard	100.011.906
EC Number	213-096-6
KEGG	C00438^Y
MeSH	ureidosuccinic+acid
PubChem	279 1550569 R 93072 S
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)^Y Key: HLKXYZVTANABHZ-UHFFFAOYSA-N^Y
SMILES [nH2]:c(:[o]):[nH]C(Cc(:[o]):[oH])c(:[o]):[oH] NC(=O)NC(CC(O)=O)C(O)=O
Properties
Chemical formula	C₅H₈N₂O₅
Molar mass	176.13 g·mol⁻¹
log P	−0.663
Acidity (pK_a)	3.649
Basicity (pK_b)	10.348
Related compounds
Related alkanoic acids	3-Ureidopropionic acid beta-Ureidoisobutyric 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).
Infobox references

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

References

↑ "ureidosuccinic acid - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification. Retrieved 27 June 2012.

Anabolism

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

IMP→AMP:	Adenylosuccinate

IMP→GMP:	Xanthosine monophosphate

Catabolism

Anabolism

Catabolism

uracil:	Dihydrouracil 3-Ureidopropionic acid β-Alanine

thymine:	Dihydrothymine β-Ureidoisobutyric acid 3-Aminoisobutyric acid

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