CHEBI:17364 - D-aspartic acid

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name D-aspartic acid ChEBI ID CHEBI:17364 ChEBI ASCII Name D-aspartic acid Definition The D-enantiomer of aspartic acid. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:4108, CHEBI:20920 Supplier Information ChemicalBook:CB6373566, eMolecules:478733, ZINC000000895218 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C4H7NO4 Net Charge 0 Average Mass 133.10270 Monoisotopic Mass 133.03751 InChI InChI=1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m1/s1 InChIKey CKLJMWTZIZZHCS-UWTATZPHSA-N SMILES N[C@H](CC(O)=O)C(O)=O Metabolite of Species Details Mus musculus (NCBI:txid10090) See: PubMed Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed Arabidopsis thaliana (NCBI:txid3702) See: PubMed Homo sapiens (NCBI:txid9606) See: PubMed Roles Classification Chemical Role(s): Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Biological Role(s): mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). fundamental metabolite Any metabolite produced by all living cells. (via aspartic acid ) View more via ChEBI Ontology ChEBI Ontology Outgoing D-aspartic acid (CHEBI:17364) has role mouse metabolite (CHEBI:75771) D-aspartic acid (CHEBI:17364) is a D-α-amino acid (CHEBI:16733) D-aspartic acid (CHEBI:17364) is a aspartic acid (CHEBI:22660) D-aspartic acid (CHEBI:17364) is conjugate acid of D-aspartate(1−) (CHEBI:29990) D-aspartic acid (CHEBI:17364) is enantiomer of L-aspartic acid (CHEBI:17053) Incoming D-aspartic acid derivative (CHEBI:83979) has functional parent D-aspartic acid (CHEBI:17364) L-Lys-D-Asp (CHEBI:144741) has functional parent D-aspartic acid (CHEBI:17364) L-Orn-D-Asp (CHEBI:144746) has functional parent D-aspartic acid (CHEBI:17364) D-aspartate(1−) (CHEBI:29990) is conjugate base of D-aspartic acid (CHEBI:17364) L-aspartic acid (CHEBI:17053) is enantiomer of D-aspartic acid (CHEBI:17364) D-aspartic acid residue (CHEBI:48094) is substituent group from D-aspartic acid (CHEBI:17364) D-aspartoyl group (CHEBI:32468) is substituent group from D-aspartic acid (CHEBI:17364) IUPAC Names (2R)-2-aminobutanedioic acid D-aspartic acid Synonyms Sources (R)-2-aminobutanedioic acid ChEBI (R)-2-aminosuccinic acid ChEBI aspartic acid D-form ChemIDplus D-Asparaginsäure ChEBI D-Aspartic acid KEGG COMPOUND DAS PDBeChem Manual Xrefs Databases C00402 KEGG COMPOUND CPD-302 MetaCyc DAS PDBeChem DB02655 DrugBank HMDB0006483 HMDB View more database links Registry Numbers Types Sources 1723529 Reaxys Registry Number Reaxys 1783-96-6 CAS Registry Number KEGG COMPOUND 1783-96-6 CAS Registry Number NIST Chemistry WebBook 1783-96-6 CAS Registry Number ChemIDplus 602084 Gmelin Registry Number Gmelin Citations Types Sources 11419736 PubMed citation Europe PMC 17118457 PubMed citation Europe PMC 17407322 PubMed citation Europe PMC 18318836 PubMed citation Europe PMC 19860889 PubMed citation Europe PMC Last Modified 04 September 2019