6-hydroxynicotinic acid (CHEBI:16168)

ChEBI > Main

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name	6-hydroxynicotinic acid

ChEBI ID	CHEBI:16168

Definition	A monohydroxypyridine that is the 6-hydroxy derivative of nicotinic acid.

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:2200, CHEBI:12219, CHEBI:20731

Supplier Information

Download	Molfile XML SDF

more structures >>

Formula

C6H5NO3

Net Charge

Average Mass

139.110

Monoisotopic Mass

139.02694

InChI

InChI=1S/C6H5NO3/c8-5-2-1-4(3-7-5)6(9)10/h1-3H,(H,7,8)(H,9,10)

InChIKey

BLHCMGRVFXRYRN-UHFFFAOYSA-N

SMILES

OC(=O)C1=CC=C(O)N=C1

Metabolite of Species	Details
Mus musculus (NCBI:txid10090)	Source: BioModels - MODEL1507180067 See: PubMed
Arabidopsis thaliana (NCBI:txid3702)	Found in leaf (BTO:0000713). See: PubMed
Homo sapiens (NCBI:txid9606)	Found in urine (BTO:0001419). See: PubMed
Homo sapiens (NCBI:txid9606)	From MetaboLights See: MetaboLights Study

Roles Classification
Biological Role(s):	human urinary metabolite Any metabolite (endogenous or exogenous) found in human urine samples. Arabidopsis thaliana metabolite Any plant metabolite that is produced by Arabidopsis thaliana. mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).

ChEBI Ontology
Outgoing	6-hydroxynicotinic acid (CHEBI:16168) has functional parent nicotinic acid (CHEBI:15940) 6-hydroxynicotinic acid (CHEBI:16168) has role Arabidopsis thaliana metabolite (CHEBI:140602) 6-hydroxynicotinic acid (CHEBI:16168) has role human urinary metabolite (CHEBI:84087) 6-hydroxynicotinic acid (CHEBI:16168) has role mouse metabolite (CHEBI:75771) 6-hydroxynicotinic acid (CHEBI:16168) is a monohydroxypyridine (CHEBI:38182) 6-hydroxynicotinic acid (CHEBI:16168) is conjugate acid of 6-hydroxynicotinate(1−) (CHEBI:57664)

Incoming	6-hydroxynicotinate(1−) (CHEBI:57664) is conjugate base of 6-hydroxynicotinic acid (CHEBI:16168)

IUPAC Name

6-hydroxypyridine-3-carboxylic acid

Last Modified

16 June 2021