CHEBI:28797 - D-α-aminobutyric acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name D-α-aminobutyric acid
ChEBI ID CHEBI:28797
ChEBI ASCII Name D-alpha-aminobutyric acid
Definition An optically active form of α-aminobutyric acid having D-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:40433, CHEBI:40463, CHEBI:40527, CHEBI:4079, CHEBI:20888
Supplier Information
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Formula C4H9NO2
Net Charge 0
Average Mass 103.11980
Monoisotopic Mass 103.06333
InChI InChI=1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m1/s1
InChIKey QWCKQJZIFLGMSD-GSVOUGTGSA-N
SMILES CC[C@@H](N)C(O)=O
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): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via alpha-aminobutyric acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-α-aminobutyric acid (CHEBI:28797) is a α-aminobutyric acid (CHEBI:35621)
D-α-aminobutyric acid (CHEBI:28797) is a D-α-amino acid (CHEBI:16733)
D-α-aminobutyric acid (CHEBI:28797) is enantiomer of L-α-aminobutyric acid (CHEBI:35619)
Incoming L-α-aminobutyric acid (CHEBI:35619) is enantiomer of D-α-aminobutyric acid (CHEBI:28797)
D-α-aminobutyric acid residue (CHEBI:40550) is substituent group from D-α-aminobutyric acid (CHEBI:28797)
IUPAC Name
(2R)-2-aminobutanoic acid
Synonyms Sources
(2R)-2-aminobutyric acid ChEBI
(R)-2-Aminobutanoic acid KEGG COMPOUND
(R)-2-aminobutyric acid ChEBI
alpha-aminobutyric acid PDBeChem
D-(−)-2-aminobutyric acid ChemIDplus
D-2-Aminobutanoic acid KEGG COMPOUND
D-2-Aminobuttersäure ChEBI
D-2-Aminobutyrate KEGG COMPOUND
D-2-Aminobutyric acid KEGG COMPOUND
Manual Xrefs Databases
C02261 KEGG COMPOUND
CPD0-1952 MetaCyc
DB04454 DrugBank
DBB PDBeChem
HMDB0000650 HMDB
LMFA01100043 LIPID MAPS
View more database links
Registry Numbers Types Sources
1720934 Reaxys Registry Number Reaxys
1720934 Beilstein Registry Number Beilstein
2623-91-8 CAS Registry Number ChemIDplus
984641 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
23407 PubMed citation Europe PMC
6110424 PubMed citation Europe PMC
6148943 PubMed citation Europe PMC
Last Modified
23 October 2015