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:CB9752065, eMolecules:491943
Download Molfile XML SDF
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