CHEBI:144728 - N-[(2S)-2-aminobutanoyl]glycine

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ChEBI Name N-[(2S)-2-aminobutanoyl]glycine
ChEBI ID CHEBI:144728
ChEBI ASCII Name N-[(2S)-2-aminobutanoyl]glycine
Definition A dipeptide resulting from the formal condensation of the carboxy group of L-α-aminobutyric acid [(2S)-2-aminobutanoic acid] with the amino group of glycine.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H12N2O3
Net Charge 0
Average Mass 160.173
Monoisotopic Mass 160.08479
InChI InChI=1S/C6H12N2O3/c1-2-4(7)6(11)8-3-5(9)10/h4H,2-3,7H2,1H3,(H,8,11)(H,9,10)/t4-/m0/s1
InChIKey SVHUWZOIWWJJJM-BYPYZUCNSA-N
SMILES [C@@H](CC)(N)C(=O)NCC(=O)O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N-[(2S)-2-aminobutanoyl]glycine (CHEBI:144728) has functional parent L-α-aminobutyric acid (CHEBI:35619)
N-[(2S)-2-aminobutanoyl]glycine (CHEBI:144728) is a carboxylic acid (CHEBI:33575)
N-[(2S)-2-aminobutanoyl]glycine (CHEBI:144728) is a dipeptide (CHEBI:46761)
N-[(2S)-2-aminobutanoyl]glycine (CHEBI:144728) is a glycine derivative (CHEBI:24373)
N-[(2S)-2-aminobutanoyl]glycine (CHEBI:144728) is a primary amino compound (CHEBI:50994)
N-[(2S)-2-aminobutanoyl]glycine (CHEBI:144728) is a secondary carboxamide (CHEBI:140325)
N-[(2S)-2-aminobutanoyl]glycine (CHEBI:144728) is tautomer of N-[(2S)-2-ammoniobutanoyl]glycinate (CHEBI:144699)
Incoming N-[(2S)-2-ammoniobutanoyl]glycinate (CHEBI:144699) is tautomer of N-[(2S)-2-aminobutanoyl]glycine (CHEBI:144728)
IUPAC Names
N-(L-α-aminobutanoyl)glycine
N-[(2S)-2-aminobutanoyl]glycine
Synonyms Sources
2-[(2S)-2-aminobutanamido]acetic acid ChEBI
H-Abu-Gly-OH ChEBI
{[(2S)-2-aminobutanoyl]amino}acetic acid IUPAC
Citation Waiting for Citations Type Source
30692244 PubMed citation SUBMITTER
Last Modified
03 September 2019