Record Information
Version1.0
Creation Date2020-05-06 19:42:46 UTC
Update Date2020-05-07 14:45:10 UTC
BMDB IDBMDB0109704
Secondary Accession NumbersNone
Metabolite Identification
Common Name3-Hydroxypyridine
Description3-pyridinol, also known as 3-hydroxypyridine, belongs to the class of organic compounds known as hydroxypyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a hydroxyl group. 3-pyridinol is a very strong basic compound (based on its pKa).
Structure
Thumb
Synonyms
ValueSource
3-HydroxypyridineChEBI
3-PyridolChEBI
beta-HydroxypyridineChEBI
m-HydroxypyridineChEBI
b-HydroxypyridineGenerator
Β-hydroxypyridineGenerator
3-Hydroxypyridine hydrochlorideMeSH
3-Hydroxypyridine isomerMeSH
3-Hydroxypyridine, silver (1+) saltMeSH
3-HydroxypyridiniumMeSH
3-Hydroxypyridine, sodium saltMeSH
Chemical FormulaC5H5NO
Average Molecular Weight95.0993
Monoisotopic Molecular Weight95.037113787
IUPAC Namepyridin-3-ol
Traditional Name3-hydroxypyridine
CAS Registry NumberNot Available
SMILES
OC1=CN=CC=C1
InChI Identifier
InChI=1S/C5H5NO/c7-5-2-1-3-6-4-5/h1-4,7H
InChI KeyGRFNBEZIAWKNCO-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as hydroxypyridines. These are organic compounds containing a pyridine ring substituted at one or more positions by a hydroxyl group.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassPyridines and derivatives
Sub ClassHydroxypyridines
Direct ParentHydroxypyridines
Alternative Parents
Substituents
  • Hydroxypyridine
  • Heteroaromatic compound
  • Azacycle
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organonitrogen compound
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External Descriptors
Ontology
StatusDetected but not Quantified
OriginNot Available
BiofunctionNot Available
ApplicationNot Available
Cellular locationsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP0.08ALOGPS
logP0.45ChemAxon
logS0.72ALOGPS
pKa (Strongest Acidic)9.16ChemAxon
pKa (Strongest Basic)5.26ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area33.12 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity25.88 m³·mol⁻¹ChemAxon
Polarizability9.16 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular LocationsNot Available
Biospecimen Locations
  • Liver
  • Mammary Gland
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
LiverDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal
details
Mammary GlandDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal
details
Abnormal Concentrations
Not Available
HMDB IDHMDB0062033
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDCPD-12318
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound7971
PDB IDNot Available
ChEBI ID87440
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available