CHEBI:16168 - 6-hydroxynicotinic acid

ChEBI IDCHEBI:16168
ChEBI Name6-hydroxynicotinic acid
Stars
DefinitionA monohydroxypyridine that is the 6-hydroxy derivative of nicotinic acid.
Secondary ChEBI IDsCHEBI:2200, CHEBI:12219, CHEBI:20731
Last Modified16 June 2021
DownloadsMolfile
FormulaC6H5NO3
Net Charge0
Average Mass139.110
Monoisotopic Mass139.02694
SMILESO=C(O)c1ccc(O)nc1
InChIInChI=1S/C6H5NO3/c8-5-2-1-4(3-7-5)6(9)10/h1-3H,(H,7,8)(H,9,10)
InChIKeyBLHCMGRVFXRYRN-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Homo sapiens (ncbitaxon:9606)
urine (BTO:0001419) PubMed (21389975)
- MetaboLights (MTBLS20) From MetaboLights
Mus musculus (ncbitaxon:10090) - PubMed (19425150) Source: BioModels - MODEL1507180067
Arabidopsis thaliana (ncbitaxon:3702) leaf (BTO:0000713) PubMed (10952545)
Roles Classification
Biological Roles:
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
Arabidopsis thaliana metabolite  Any plant metabolite that is produced by Arabidopsis thaliana.
human urinary metabolite  Any metabolite (endogenous or exogenous) found in human urine samples.
ChEBI Ontology
Outgoing Relation(s)
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 Relation(s)
6-hydroxynicotinate(1−) (CHEBI:57664) is conjugate base of 6-hydroxynicotinic acid (CHEBI:16168)
IUPAC Name 
6-hydroxypyridine-3-carboxylic acid
Synonyms  Source
6-HydroxynicotinateKEGG COMPOUND
6-Hydroxynicotinic acidKEGG COMPOUND
Manual XrefsDatabases
C01020KEGG COMPOUND
HMDB0002658HMDB
FDB023041FooDB
C00007415KNApSAcK
OA7PDBeChem
65756ChemSpider
EP0152949Patent
EP0152948Patent
Registry NumbersSources
Reaxys:115991Reaxys
CAS:5006-66-6NIST Chemistry WebBook
CAS:5006-66-6ChemIDplus
Citations