CHEBI:62412 - phenazine-1-carboxylic acid

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ChEBI Name phenazine-1-carboxylic acid
ChEBI ID CHEBI:62412
Definition An aromatic carboxylic acid that is phenazine substituted at C-1 with a carboxy group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C13H8N2O2
Net Charge 0
Average Mass 224.21480
Monoisotopic Mass 224.059
InChI InChI=1S/C13H8N2O2/c16-13(17)8-4-3-7-11-12(8)15-10-6-2-1-5-9(10)14-11/h1-7H,(H,16,17)
InChIKey JGCSKOVQDXEQHI-UHFFFAOYSA-N
SMILES OC(=O)c1cccc2nc3ccccc3nc12
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): antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antifungal agent
An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing phenazine-1-carboxylic acid (CHEBI:62412) has role antifungal agent (CHEBI:35718)
phenazine-1-carboxylic acid (CHEBI:62412) has role antimicrobial agent (CHEBI:33281)
phenazine-1-carboxylic acid (CHEBI:62412) has role bacterial metabolite (CHEBI:76969)
phenazine-1-carboxylic acid (CHEBI:62412) is a aromatic carboxylic acid (CHEBI:33859)
phenazine-1-carboxylic acid (CHEBI:62412) is a monocarboxylic acid (CHEBI:25384)
phenazine-1-carboxylic acid (CHEBI:62412) is a phenazines (CHEBI:39201)
phenazine-1-carboxylic acid (CHEBI:62412) is conjugate acid of phenazine-1-carboxylate (CHEBI:62248)
Incoming phenazine-1-carboxylate (CHEBI:62248) is conjugate base of phenazine-1-carboxylic acid (CHEBI:62412)
Synonyms Sources
1-Carboxylic acid phenazine ChemIDplus
1-carboxyphenazine ChEBI
1-Phenazinecarboxylic acid ChemIDplus
Phenazin-1-carbonsäure ChEBI
Phenazinecarboxylic acid ChemIDplus
Manual Xrefs Databases
3032 BPDB
CPD-9522 MetaCyc
View more database links
Registry Numbers Types Sources
183818 Beilstein Registry Number ChemIDplus
183818 Reaxys Registry Number Reaxys
2538-68-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
12458768 PubMed citation Europe PMC
14711317 PubMed citation Europe PMC
22138981 PubMed citation Europe PMC
22724439 PubMed citation Europe PMC
23636695 PubMed citation Europe PMC
Last Modified
12 March 2014