CHEBI:35619 - L-α-aminobutyric acid

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ChEBI Name L-α-aminobutyric acid
ChEBI ID CHEBI:35619
ChEBI ASCII Name L-alpha-aminobutyric acid
Definition An optically active form of α-aminobutyric acid having L-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:35723, CHEBI:376, CHEBI:46346, CHEBI:18734
Supplier Information
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Formula C4H9NO2
Net Charge 0
Average Mass 103.11980
Monoisotopic Mass 103.063
InChI InChI=1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1
InChIKey QWCKQJZIFLGMSD-VKHMYHEASA-N
SMILES CC[C@H](N)C(O)=O
Metabolite of Species Details
Homo sapiens (NCBI:9606) See: DOI
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via alpha-aminobutyric acid )
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing L-α-aminobutyric acid (CHEBI:35619) has role human metabolite (CHEBI:77746)
L-α-aminobutyric acid (CHEBI:35619) is a α-aminobutyric acid (CHEBI:35621)
L-α-aminobutyric acid (CHEBI:35619) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
L-α-aminobutyric acid (CHEBI:35619) is conjugate acid of L-2-aminobutyrate (CHEBI:28340)
L-α-aminobutyric acid (CHEBI:35619) is enantiomer of D-α-aminobutyric acid (CHEBI:28797)
L-α-aminobutyric acid (CHEBI:35619) is tautomer of L-α-aminobutyrate zwitterion (CHEBI:74359)
Incoming L-2-amino-4-methoxy-cis-but-3-enoic acid (CHEBI:40719) has functional parent L-α-aminobutyric acid (CHEBI:35619)
L-2-aminobutyrate (CHEBI:28340) is conjugate base of L-α-aminobutyric acid (CHEBI:35619)
D-α-aminobutyric acid (CHEBI:28797) is enantiomer of L-α-aminobutyric acid (CHEBI:35619)
L-α-aminobutyric acid residue (CHEBI:40545) is substituent group from L-α-aminobutyric acid (CHEBI:35619)
L-α-aminobutyrate zwitterion (CHEBI:74359) is tautomer of L-α-aminobutyric acid (CHEBI:35619)
IUPAC Name
(2S)-2-aminobutanoic acid
Synonyms Sources
(−)-2-aminobutyric acid ChemIDplus
(2S)-2-aminobutyric acid ChEBI
(S)-2-Aminobutanoate KEGG COMPOUND
(S)-2-Aminobutanoic acid KEGG COMPOUND
(S)-2-Aminobutyric acid KEGG COMPOUND
L-(+)-2-aminobutyric acid ChEBI
L-2-Aminobuttersäure ChEBI
L-2-aminobutyric acid ChemIDplus
L-α-amino-n-butyric acid NIST Chemistry WebBook
L-α-aminobutyric acid NIST Chemistry WebBook
L-butyrine ChemIDplus
S-Butyrine HMDB
Database Links Databases
AA0409 RESID
ABA PDBeChem
C02356 KEGG COMPOUND
CPD0-1942 MetaCyc
HMDB00452 HMDB
LMFA01100034 LIPID MAPS
YMDB01570 YMDB
View more database links
Registry Numbers Types Sources
1492-24-6 CAS Registry Number ChemIDplus
1492-24-6 CAS Registry Number NIST Chemistry WebBook
1720935 Reaxys Registry Number Reaxys
1720935 Beilstein Registry Number Beilstein
278145 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
16098526 PubMed citation Europe PMC
1700029 PubMed citation Europe PMC
4572987 PubMed citation Europe PMC
575311 PubMed citation Europe PMC
Last Modified
23 October 2015