Date published: 2025-12-1

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N-Carbamoyl-DL-aspartic acid (CAS 923-37-5)

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Alternate Names:
Ureidosuccinic acid
Application:
N-Carbamoyl-DL-aspartic acid is a useful biochemical for proteomics research
CAS Number:
923-37-5
Purity:
≥95%
Molecular Weight:
176.13
Molecular Formula:
C5H8N2O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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N-Carbamoyl-DL-aspartic acid, also known as N-Carbamoylaspartate, is an intermediate compound in the urea cycle and nucleotide biosynthesis pathways, playing a pivotal role in the metabolic framework of various organisms. This compound is synthesized through the condensation of carbamoyl phosphate and aspartate, a reaction catalyzed by the enzyme aspartate transcarbamoylase. This process is critical in the synthesis of pyrimidines, where N-Carbamoyl-DL-aspartic acid acts as a precursor for the production of cytosine, thymine, and uracil, fundamental components of the genetic material in cells. In research, N-Carbamoyl-DL-aspartic acid is utilized to study enzymatic activities within the urea and pyrimidine biosynthesis pathways, offering insights into genetic regulation, enzyme kinetics, and pathway optimization. Its role extends to the exploration of metabolic diseases related to nucleotide synthesis dysregulation, serving as a tool in dissecting the complex interactions within cellular metabolic networks.


N-Carbamoyl-DL-aspartic acid (CAS 923-37-5) References

  1. Structural and biochemical characterization of the biuret hydrolase (BiuH) from the cyanuric acid catabolism pathway of Rhizobium leguminasorum bv. viciae 3841.  |  Esquirol, L., et al. 2018. PLoS One. 13: e0192736. PMID: 29425231
  2. Purification, characterization and inhibition of dihydropyrimidinase from rat liver.  |  Kikugawa, M., et al. 1994. Eur J Biochem. 219: 393-9. PMID: 8307005
  3. Synthesis, crystal structure and hydrogen-bonding patterns in (RS)-1-carbamoyl pyrrolidine-2-carboxylic acid  |  GE Delgado, LE Seijas, AJ Mora, T González. 2012. Journal of Chemical Crystallography. 42: 388–393.
  4. EPR studies of the free radicals generated in gamma irradiated amino acid derivativesIF 3.841Q3B3EI  |  YE Osmanoğlu, K Sütçü. 2017. Journal of Molecular Structure. 1145: 240-243.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Carbamoyl-DL-aspartic acid, 1 g

sc-281065
1 g
$107.00