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Carbamoyl aspartic acid information


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
SMILES
  • 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
  • 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, serving as an intermediate in pyrimidine biosynthesis.

  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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Carbamoyl aspartic acid

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

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Dihydroorotase

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converts carbamoyl aspartic acid into 4,5-dihydroorotic acid in the biosynthesis of pyrimidines. It forms a multifunctional enzyme with carbamoyl phosphate...

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Nucleotide

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aspartate and carbamoyl phosphate to form carbamoyl aspartic acid, which is cyclized into 4,5-dihydroorotic acid by dihydroorotase. The latter is converted...

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Pyrimidine metabolism

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of the process are all coded by the same gene in CAD which consists of carbamoyl phosphate synthetase II, aspartate carbamoyltransferase and dihydroorotase...

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Ornithine

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into carbamoyl phosphate (H 2NC(O)OPO2− 3) by carbamoyl phosphate synthetase. Ornithine transcarbamylase catalyzes the reaction between carbamoyl phosphate...

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C5H8N2O5

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exact mass: 176.0433 u) may refer to: Carbamoyl aspartic acid (or ureidosuccinic acid) Oxalyldiaminopropionic acid This set index page lists chemical structure...

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Argininosuccinic acid

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cycle. Some cells synthesize argininosuccinic acid from citrulline and aspartic acid and use it as a precursor for arginine in the urea cycle or citrulline-NO...

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Bromisoval

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bromine poisoning. Bromisoval can be prepared by bromination of isovaleric acid by the Hell-Volhard-Zelinsky reaction followed by reaction with urea. Acecarbromal...

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Carbromal

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pentobarbital, under the name Carbrital. Diethylmalonic acid [510-20-3] (1) is decarboxylated to 2-ethylvaleric acid [20225-24-5] (2). The Hell-Volhard-Zelinsky reaction...

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Transferase

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carboxy, carbamoyl, and amido groups. Carbamoyltransferases, as an example, transfer a carbamoyl group from one molecule to another. Carbamoyl groups follow...

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Glutamine synthetase

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inhibitors are the result of glutamine metabolism: tryptophan, histidine, carbamoyl phosphate, glucosamine-6-phosphate, cytidine triphosphate (CTP), and adenosine...

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Nicotinamide riboside

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influenza cannot grow on nicotinic acid (NA), nicotinamide (NAM), or amino acids such as tryptophan (Trp) or aspartic acid (Asp), which were the previously...

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