CHEBI:30754 - anthranilic acid

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ChEBI Name anthranilic acid
ChEBI ID CHEBI:30754
Definition An aminobenzoic acid that is benzoic acid having a single amino substituent located at position 2. It is a metabolite produced in L-tryptophan-kynurenine pathway in the central nervous system.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:40980, CHEBI:2757, CHEBI:22577, CHEBI:22578
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Formula C7H7NO2
Net Charge 0
Average Mass 137.13600
Monoisotopic Mass 137.04768
InChI InChI=1S/C7H7NO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,8H2,(H,9,10)
InChIKey RWZYAGGXGHYGMB-UHFFFAOYSA-N
SMILES Nc1ccccc1C(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 (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).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing anthranilic acid (CHEBI:30754) has role human metabolite (CHEBI:77746)
anthranilic acid (CHEBI:30754) has role mouse metabolite (CHEBI:75771)
anthranilic acid (CHEBI:30754) is a aminobenzoic acid (CHEBI:22495)
anthranilic acid (CHEBI:30754) is conjugate acid of anthranilate (CHEBI:16567)
Incoming 1-(2-carboxyphenylamino)-1-deoxy-D-ribulose 5-phosphate (CHEBI:29112) has functional parent anthranilic acid (CHEBI:30754)
1-azepanyl-[2-[4-(difluoromethylthio)anilino]phenyl]methanone (CHEBI:116306) has functional parent anthranilic acid (CHEBI:30754)
2-(Ethylamino)-4,5-dihydroxybenzamide (CHEBI:165205) has functional parent anthranilic acid (CHEBI:30754)
2-(oxaloamino)benzoic acid (CHEBI:44493) has functional parent anthranilic acid (CHEBI:30754)
2-[[1-oxo-3-(4-pentylphenyl)prop-2-enyl]amino]benzoic acid (CHEBI:114200) has functional parent anthranilic acid (CHEBI:30754)
2-[[3-(3,4-dimethoxyphenyl)-1-oxoprop-2-enyl]amino]benzoic acid (CHEBI:92320) has functional parent anthranilic acid (CHEBI:30754)
2-[[3-(4-methoxyphenyl)-1-oxoprop-2-enyl]amino]benzoic acid (CHEBI:105696) has functional parent anthranilic acid (CHEBI:30754)
2-amino-5-[(1-methoxy-2-methylindolizin-3-yl)carbonyl]benzoic acid (CHEBI:73307) has functional parent anthranilic acid (CHEBI:30754)
3,5-dihydroxyanthranilic acid (CHEBI:1403) has functional parent anthranilic acid (CHEBI:30754)
3-(1-carboxyvinyloxy)anthranilic acid (CHEBI:49194) has functional parent anthranilic acid (CHEBI:30754)
3-hydroxy-4-methylanthranilic acid (CHEBI:16116) has functional parent anthranilic acid (CHEBI:30754)
3-hydroxyanthranilic acid (CHEBI:15793) has functional parent anthranilic acid (CHEBI:30754)
3-methoxyanthranilic acid (CHEBI:27440) has functional parent anthranilic acid (CHEBI:30754)
4-nitroanthranilic acid (CHEBI:75335) has functional parent anthranilic acid (CHEBI:30754)
5-fluoroanthranilic acid (CHEBI:78042) has functional parent anthranilic acid (CHEBI:30754)
N-(5-phospho-β-D-ribosyl)anthranilic acid (CHEBI:7091) has functional parent anthranilic acid (CHEBI:30754)
N-acetylanthranilic acid (CHEBI:36555) has functional parent anthranilic acid (CHEBI:30754)
N-adenylylanthranilic acid (CHEBI:17469) has functional parent anthranilic acid (CHEBI:30754)
N-benzoyl-4-hydroxyanthranilic acid (CHEBI:16606) has functional parent anthranilic acid (CHEBI:30754)
N-benzoyl-4-methoxyanthranilic acid (CHEBI:28609) has functional parent anthranilic acid (CHEBI:30754)
N-benzoylanthranilic acid (CHEBI:50037) has functional parent anthranilic acid (CHEBI:30754)
N-formylanthranilic acid (CHEBI:36575) has functional parent anthranilic acid (CHEBI:30754)
N-malonylanthranilic acid (CHEBI:52430) has functional parent anthranilic acid (CHEBI:30754)
N-methylanthranilic acid (CHEBI:16394) has functional parent anthranilic acid (CHEBI:30754)
N-octanoylanthranilic acid (CHEBI:143902) has functional parent anthranilic acid (CHEBI:30754)
S-anthraniloyl-L-cysteine (CHEBI:134405) has functional parent anthranilic acid (CHEBI:30754)
ANA-12 (CHEBI:140465) has functional parent anthranilic acid (CHEBI:30754)
anthraniloyl-CoA (CHEBI:15472) has functional parent anthranilic acid (CHEBI:30754)
butyl anthranilate (CHEBI:86192) has functional parent anthranilic acid (CHEBI:30754)
fenamic acid (CHEBI:34756) has functional parent anthranilic acid (CHEBI:30754)
flufenamate (CHEBI:520819) has functional parent anthranilic acid (CHEBI:30754)
flufenamic acid (CHEBI:42638) has functional parent anthranilic acid (CHEBI:30754)
glafenine (CHEBI:31653) has functional parent anthranilic acid (CHEBI:30754)
methyl anthranilate (CHEBI:73244) has functional parent anthranilic acid (CHEBI:30754)
N1-[2-(2-pyridyl)ethyl]-2-aminobenzamide (CHEBI:183710) has functional parent anthranilic acid (CHEBI:30754)
onosmin A (CHEBI:66821) has functional parent anthranilic acid (CHEBI:30754)
sirtinol (CHEBI:73158) has functional parent anthranilic acid (CHEBI:30754)
terreazepine (CHEBI:167044) has functional parent anthranilic acid (CHEBI:30754)
tolfenamic acid (CHEBI:32243) has functional parent anthranilic acid (CHEBI:30754)
tranilast (CHEBI:77572) has functional parent anthranilic acid (CHEBI:30754)
anthranilate (CHEBI:16567) is conjugate base of anthranilic acid (CHEBI:30754)
IUPAC Name
2-aminobenzoic acid
Synonyms Sources
2-Aminobenzoesäure ChEBI
2-AMINOBENZOIC ACID PDBeChem
2-carboxyaniline NIST Chemistry WebBook
Anthranilic acid KEGG COMPOUND
o-Aminobenzoesäure ChEBI
o-Aminobenzoic acid KEGG COMPOUND
o-aminobenzoic acid NIST Chemistry WebBook
o-carboxyaniline NIST Chemistry WebBook
Vitamin L1 KEGG COMPOUND
Manual Xrefs Databases
ANTHRANILATE MetaCyc
Anthranilic_acid Wikipedia
BE2 PDBeChem
C00007382 KNApSAcK
C00108 KEGG COMPOUND
DB04166 DrugBank
HMDB0001123 HMDB
View more database links
Registry Numbers Types Sources
118-92-3 CAS Registry Number KEGG COMPOUND
118-92-3 CAS Registry Number ChemIDplus
118-92-3 CAS Registry Number NIST Chemistry WebBook
3397 Gmelin Registry Number Gmelin
471803 Reaxys Registry Number Reaxys
471803 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
11680877 PubMed citation Europe PMC
19745702 PubMed citation Europe PMC
20511543 PubMed citation Europe PMC
22321994 PubMed citation Europe PMC
22341575 PubMed citation Europe PMC
22784643 PubMed citation Europe PMC
28166217 PubMed citation Europe PMC
9784247 PubMed citation Europe PMC
Last Modified
04 August 2021
General Comment
2021-08-04 Formerly believed to be a vitamin but is now known to be non-essential in human nutrition.