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> Main
CHEBI:35621 - α-aminobutyric acid
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ChEBI Name
α-aminobutyric acid
ChEBI ID
CHEBI:35621
ChEBI ASCII Name
alpha-aminobutyric acid
Definition
An α-amino acid that is butyric acid bearing a single amino substituent located at position 2.
Stars
This entity has been manually annotated by the ChEBI Team.
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Read full article at Wikipedia
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)
InChIKey
QWCKQJZIFLGMSD-UHFFFAOYSA-N
SMILES
CCC(N)C(O)=O
Metabolite of Species
Details
Homo sapiens
(NCBI:txid9606)
See:
PubMed
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Br
o
nsted acid).
(via
organic amino compound
)
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
α-aminobutyric acid (
CHEBI:35621
)
has functional parent
butyric acid (
CHEBI:30772
)
α-aminobutyric acid (
CHEBI:35621
)
has role
human metabolite (
CHEBI:77746
)
α-aminobutyric acid (
CHEBI:35621
)
is a
monocarboxylic acid (
CHEBI:25384
)
α-aminobutyric acid (
CHEBI:35621
)
is a
non-proteinogenic α-amino acid (
CHEBI:83925
)
α-aminobutyric acid (
CHEBI:35621
)
is conjugate acid of
α-aminobutyrate (
CHEBI:86508
)
Incoming
D
-α-aminobutyric acid (
CHEBI:28797
)
is a
α-aminobutyric acid (
CHEBI:35621
)
L
-α-aminobutyric acid (
CHEBI:35619
)
is a
α-aminobutyric acid (
CHEBI:35621
)
α-aminobutyrate (
CHEBI:86508
)
is conjugate base of
α-aminobutyric acid (
CHEBI:35621
)
IUPAC Name
2-aminobutanoic acid
Synonyms
Sources
2-amino-
n
-butyric acid
NIST Chemistry WebBook
2-aminobutyric acid
ChemIDplus
AABA
NIST Chemistry WebBook
Abu
ChEBI
α-amino-
n
-butyric acid
NIST Chemistry WebBook
α-aminobutyric acid
NIST Chemistry WebBook
butyrine
ChemIDplus
homoalanine
ChEBI
Manual Xrefs
Databases
Alpha-Aminobutyric_acid
Wikipedia
CPD-3686
MetaCyc
DB04454
DrugBank
View more database links
Registry Numbers
Types
Sources
217679
Gmelin Registry Number
Gmelin
2835-81-6
CAS Registry Number
NIST Chemistry WebBook
2835-81-6
CAS Registry Number
ChemIDplus
635889
Reaxys Registry Number
Reaxys
635889
Beilstein Registry Number
Beilstein
Citations
Types
Sources
11958629
PubMed citation
Europe PMC
15246869
PubMed citation
Europe PMC
20551690
PubMed citation
Europe PMC
22061039
PubMed citation
Europe PMC
22264337
PubMed citation
Europe PMC
22770225
PubMed citation
Europe PMC
Last Modified
16 July 2015