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:
human urinary metabolite  Any metabolite (endogenous or exogenous) found in human urine samples.
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.
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