Showing metabocard for 3-Succinoylpyridine (BMDB0000992)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-09-30 22:39:36 UTC
Update Date2020-04-22 15:06:14 UTC
BMDB IDBMDB0000992
Secondary Accession Numbers
  • BMDB00992
Metabolite Identification
Common Name3-Succinoylpyridine
Description3-Succinoylpyridine, also known as 4-OPC4a, belongs to the class of organic compounds known as gamma-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the C4 carbon atom. Based on a literature review a significant number of articles have been published on 3-Succinoylpyridine.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
4-oxo-4-(3-Pyridyl)-butanoic acidChEBI
4-oxo-4-(3-Pyridyl)-butyric acidChEBI
4-oxo-4-(Pyridin-3-yl)butyric acidChEBI
gamma-oxo-3-Pyridinebutanoic acidChEBI
gamma-oxo-3-Pyridinebutyric acidChEBI
4-oxo-4-(Pyridin-3-yl)butanoateKegg
4-oxo-4-(3-Pyridyl)-butanoateGenerator
4-oxo-4-(3-Pyridyl)-butyrateGenerator
4-oxo-4-(Pyridin-3-yl)butyrateGenerator
g-oxo-3-PyridinebutanoateGenerator
g-oxo-3-Pyridinebutanoic acidGenerator
gamma-oxo-3-PyridinebutanoateGenerator
Γ-oxo-3-pyridinebutanoateGenerator
Γ-oxo-3-pyridinebutanoic acidGenerator
g-oxo-3-PyridinebutyrateGenerator
g-oxo-3-Pyridinebutyric acidGenerator
gamma-oxo-3-PyridinebutyrateGenerator
Γ-oxo-3-pyridinebutyrateGenerator
Γ-oxo-3-pyridinebutyric acidGenerator
4-oxo-4-(Pyridin-3-yl)butanoic acidGenerator
4-OPC4aHMDB
4-oxo-4-(3-Pyridyl)butanoic acidHMDB
4-oxo-4-(3-Pyridyl)butyric acidHMDB
3-SuccinoylpyridineChEBI
Chemical FormulaC9H9NO3
Average Molecular Weight179.1727
Monoisotopic Molecular Weight179.058243159
IUPAC Name4-oxo-4-(pyridin-3-yl)butanoic acid
Traditional Name3-succinoylpyridine
CAS Registry Number4192-31-8
SMILES
OC(=O)CCC(=O)C1=CC=CN=C1
InChI Identifier
InChI=1S/C9H9NO3/c11-8(3-4-9(12)13)7-2-1-5-10-6-7/h1-2,5-6H,3-4H2,(H,12,13)
InChI KeyJGSUNMCABQUBOY-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as gamma-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the C4 carbon atom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassKeto acids and derivatives
Sub ClassGamma-keto acids and derivatives
Direct ParentGamma-keto acids and derivatives
Alternative Parents
Substituents
  • Gamma-keto acid
  • Aryl ketone
  • Aryl alkyl ketone
  • Pyridine
  • Heteroaromatic compound
  • Ketone
  • Azacycle
  • Organoheterocyclic compound
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic nitrogen compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External Descriptors
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locationsNot Available
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP0.08ALOGPS
logP-0.58ChemAxon
logS-1.3ALOGPS
pKa (Strongest Acidic)3.36ChemAxon
pKa (Strongest Basic)4ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area67.26 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity45.2 m³·mol⁻¹ChemAxon
Polarizability17.56 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0000992
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB022355
KNApSAcK IDNot Available
Chemspider ID424
KEGG Compound IDC19569
BioCyc IDCPD-14094
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN ID5924
PubChem Compound437
PDB IDNot Available
ChEBI ID66951
References
Synthesis ReferenceSchwartz, Sorell L.; McKennis, Herbert, Jr. The degradation of the pyrrolidine ring of (-)-nicotine in vitro. Formation of g-(3-pyridyl)-g-oxobutyric acid. Journal of Biological Chemistry (1963), 238 1807-12.
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available