U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C5H8N2O5
Molecular Weight 176.1274
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-CARBAMOYLASPARTIC ACID

SMILES

NC(=O)N[C@@H](CC(O)=O)C(O)=O

InChI

InChIKey=HLKXYZVTANABHZ-REOHCLBHSA-N
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)/t2-/m0/s1

HIDE SMILES / InChI

Molecular Formula C5H8N2O5
Molecular Weight 176.1274
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Regulation of pyrimidine nucleotide formation in Pseudomonas reptilivora.
2004
Dissection and design of yeast prions.
2004 Apr
Molecular cloning and biochemical characterization of L-N-carbamoylase from Sinorhizobium meliloti CECT4114.
2005
Harnessing natural diversity to probe metabolic pathways.
2005 Dec
Nitrogen source and the retrograde signalling pathway affect detection, not generation, of the [URE3] prion.
2006 Aug
13C and 15N isotope effects for conversion of L-dihydroorotate to N-carbamyl-L-aspartate using dihydroorotase from hamster and Bacillus caldolyticus.
2006 Jun 13
How to find a prion: [URE3], [PSI+] and [beta].
2006 May
Reporter assay systems for [URE3] detection and analysis.
2006 May
Mutations in yhiT enable utilization of exogenous pyrimidine intermediates in Salmonella enterica serovar Typhimurium.
2007 Aug
Differential regulation and substrate preferences in two peptide transporters of Saccharomyces cerevisiae.
2007 Oct
Complex evolution of the DAL5 transporter family.
2008 Apr 11
Extra N-terminal residues have a profound effect on the aggregation properties of the potential yeast prion protein Mca1.
2010 Mar 29
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:46:05 GMT 2023
Edited
by admin
on Sat Dec 16 10:46:05 GMT 2023
Record UNII
R2521024DK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-CARBAMOYLASPARTIC ACID
Systematic Name English
N-CARBAMYLASPARTIC ACID
Systematic Name English
L-UREIDOSUCCINIC ACID
Common Name English
L-ASPARTIC ACID, N-(AMINOCARBONYL)-
Systematic Name English
NSC-14983
Code English
CARBAMOYLASPARTIC ACID
Systematic Name English
N-CARBAMOYL-L-ASPARTIC ACID
Systematic Name English
CARBAMYLASPARTIC ACID
Systematic Name English
N-CARBAMOYL-(S)-ASPARTIC ACID
Systematic Name English
Code System Code Type Description
FDA UNII
R2521024DK
Created by admin on Sat Dec 16 10:46:05 GMT 2023 , Edited by admin on Sat Dec 16 10:46:05 GMT 2023
PRIMARY
EPA CompTox
DTXSID30864374
Created by admin on Sat Dec 16 10:46:05 GMT 2023 , Edited by admin on Sat Dec 16 10:46:05 GMT 2023
PRIMARY
PUBCHEM
93072
Created by admin on Sat Dec 16 10:46:05 GMT 2023 , Edited by admin on Sat Dec 16 10:46:05 GMT 2023
PRIMARY
CAS
13184-27-5
Created by admin on Sat Dec 16 10:46:05 GMT 2023 , Edited by admin on Sat Dec 16 10:46:05 GMT 2023
PRIMARY
ECHA (EC/EINECS)
236-134-3
Created by admin on Sat Dec 16 10:46:05 GMT 2023 , Edited by admin on Sat Dec 16 10:46:05 GMT 2023
PRIMARY
CHEBI
64850
Created by admin on Sat Dec 16 10:46:05 GMT 2023 , Edited by admin on Sat Dec 16 10:46:05 GMT 2023
PRIMARY
CHEBI
15859
Created by admin on Sat Dec 16 10:46:05 GMT 2023 , Edited by admin on Sat Dec 16 10:46:05 GMT 2023
PRIMARY
NSC
14983
Created by admin on Sat Dec 16 10:46:05 GMT 2023 , Edited by admin on Sat Dec 16 10:46:05 GMT 2023
PRIMARY