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> Main
CHEBI:30753 - 4-aminobenzoic acid
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ChEBI Name
4-aminobenzoic acid
ChEBI ID
CHEBI:30753
Definition
An aminobenzoic acid in which the amino group is
para
to the carboxy group.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:44778, CHEBI:113372, CHEBI:1783, CHEBI:20315
Supplier Information
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Wikipedia
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Read full article at Wikipedia
Formula
C7H7NO2
Net Charge
0
Average Mass
137.136
Monoisotopic Mass
137.04768
InChI
InChI=1S/C7H7NO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H,9,10)
InChIKey
ALYNCZNDIQEVRV-UHFFFAOYSA-N
SMILES
C1(C(O)=O)=CC=C(N)C=C1
Metabolite of Species
Details
Arabidopsis thaliana
(NCBI:txid3702)
See:
PubMed
Escherichia coli
(NCBI:txid562)
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):
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in
Escherichia coli
.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
allergen
A chemical compound, or part thereof, which causes the onset of an allergic reaction by interacting with any of the molecular pathways involved in an allergy.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
4-aminobenzoic acid (
CHEBI:30753
)
has functional parent
benzoic acid (
CHEBI:30746
)
4-aminobenzoic acid (
CHEBI:30753
)
has role
Escherichia coli
metabolite (
CHEBI:76971
)
4-aminobenzoic acid (
CHEBI:30753
)
has role
allergen (
CHEBI:50904
)
4-aminobenzoic acid (
CHEBI:30753
)
has role
plant metabolite (
CHEBI:76924
)
4-aminobenzoic acid (
CHEBI:30753
)
is a
aminobenzoic acid (
CHEBI:22495
)
4-aminobenzoic acid (
CHEBI:30753
)
is conjugate acid of
4-aminobenzoate (
CHEBI:17836
)
4-aminobenzoic acid (
CHEBI:30753
)
is conjugate base of
4-carboxyanilinium (
CHEBI:194473
)
4-aminobenzoic acid (
CHEBI:30753
)
is tautomer of
4-ammoniobenzoate (
CHEBI:194474
)
Incoming
4-(hydroxyamino)benzoic acid (
CHEBI:231474
)
has functional parent
4-aminobenzoic acid (
CHEBI:30753
)
4-(oxaloamino)benzoic acid (
CHEBI:30875
)
has functional parent
4-aminobenzoic acid (
CHEBI:30753
)
4-acetamidobenzoic acid (
CHEBI:46171
)
has functional parent
4-aminobenzoic acid (
CHEBI:30753
)
ascr#8 (
CHEBI:78834
)
has functional parent
4-aminobenzoic acid (
CHEBI:30753
)
butamben (
CHEBI:3231
)
has functional parent
4-aminobenzoic acid (
CHEBI:30753
)
procaine (
CHEBI:8430
)
has functional parent
4-aminobenzoic acid (
CHEBI:30753
)
4-carboxyanilinium (
CHEBI:194473
)
is conjugate acid of
4-aminobenzoic acid (
CHEBI:30753
)
4-aminobenzoate (
CHEBI:17836
)
is conjugate base of
4-aminobenzoic acid (
CHEBI:30753
)
4-ammoniobenzoate (
CHEBI:194474
)
is tautomer of
4-aminobenzoic acid (
CHEBI:30753
)
IUPAC Name
4-aminobenzoic acid
Synonyms
Sources
1-Amino-4-carboxybenzene
HMDB
4-Amino-benzoic acid
ChEMBL
4-Aminobenzoesäure
ChEBI
4-Aminobenzoic acid
KEGG COMPOUND
4-AMINOBENZOIC ACID
PDBeChem
4-Carboxyaniline
HMDB
4-Carboxyphenylamine
HMDB
ABEE
KEGG COMPOUND
γ-aminobenzoic acid
HMDB
gamma-Aminobenzoic acid
HMDB
p
-Aminobenzoesäure
ChEBI
p
-aminobenzoic acid
NIST Chemistry WebBook
p
-carboxyaniline
HMDB
p
-carboxyphenylamine
HMDB
PABA
NIST Chemistry WebBook
para
-aminobenzoic acid
NIST Chemistry WebBook
Manual Xrefs
Databases
2049
DrugCentral
4-Aminobenzoic_acid
Wikipedia
C00001401
KNApSAcK
C00568
KEGG COMPOUND
D02456
KEGG DRUG
DB02362
DrugBank
ECMDB01392
ECMDB
HMDB0001392
HMDB
PAB
PDBeChem
YMDB00493
YMDB
View more database links
Registry Numbers
Types
Sources
150-13-0
CAS Registry Number
KEGG COMPOUND
150-13-0
CAS Registry Number
NIST Chemistry WebBook
150-13-0
CAS Registry Number
ChemIDplus
471605
Reaxys Registry Number
Reaxys
50150
Gmelin Registry Number
Gmelin
Citations
Types
Sources
12039592
PubMed citation
ChEMBL
14745019
PubMed citation
Europe PMC
15115392
PubMed citation
ChEMBL
1527790
PubMed citation
ChEMBL
16290145
PubMed citation
ChEMBL
17149871
PubMed citation
ChEMBL
17743450
PubMed citation
Europe PMC
17800214
PubMed citation
Europe PMC
19469519
PubMed citation
Europe PMC
22767283
PubMed citation
Europe PMC
22994574
PubMed citation
Europe PMC
23063996
PubMed citation
Europe PMC
23084339
PubMed citation
Europe PMC
23144588
PubMed citation
Europe PMC
23471007
PubMed citation
Europe PMC
3599019
PubMed citation
ChEMBL
3820215
PubMed citation
ChEMBL
3950915
PubMed citation
ChEMBL
8411009
PubMed citation
ChEMBL
9406595
PubMed citation
ChEMBL
Last Modified
28 May 2024