Showing Compound Card for 5H-cyclopenta[b]pyridin-6(7H)-one (CDB005999)

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Record Information
Version1.0
Created at2020-04-27 17:18:53 UTC
Updated at2021-01-06 19:07:00 UTC
CannabisDB IDCDB005999
Secondary Accession NumbersNot Available
Cannabis Compound Identification
Common Name5H-cyclopenta[b]pyridin-6(7H)-one
Description5H-cyclopenta[b]pyridin-6(7H)-one belongs to the class of organic compounds known as pyridines and derivatives. Pyridines and derivatives are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms. 5H-cyclopenta[b]pyridin-6(7H)-one is a strong basic compound (based on its pKa). 5H-cyclopenta[b]pyridin-6(7H)-one is formed during the combustion of cannabis and is therefore a constituent of cannabis smoke ( Ref:DOI ).
Structure
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MOLSDF3D-SDFPDBSMILESInChI View 3D Structure
SynonymsNot Available
Chemical FormulaC8H7NO
Average Molecular Weight133.15
Monoisotopic Molecular Weight133.0528
IUPAC Name5H,6H,7H-cyclopenta[b]pyridin-6-one
Traditional Name5H,7H-cyclopenta[b]pyridin-6-one
CAS Registry Number1256823-82-1
SMILES
O=C1CC2=C(C1)N=CC=C2
InChI Identifier
InChI=1S/C8H7NO/c10-7-4-6-2-1-3-9-8(6)5-7/h1-3H,4-5H2
InChI KeyOVHDPSLTHBMJDM-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as pyridines and derivatives. Pyridines and derivatives are compounds containing a pyridine ring, which is a six-member aromatic heterocycle which consists of one nitrogen atom and five carbon atoms.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassPyridines and derivatives
Sub ClassNot Available
Direct ParentPyridines and derivatives
Alternative Parents
Substituents
  • Pyridine
  • Heteroaromatic compound
  • Cyclic ketone
  • Ketone
  • Azacycle
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organonitrogen compound
  • Carbonyl group
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Not 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
logP0.62ALOGPS
logP0.97ChemAxon
logS0ALOGPS
pKa (Strongest Acidic)12.96ChemAxon
pKa (Strongest Basic)4.14ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area29.96 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity37.05 m³·mol⁻¹ChemAxon
Polarizability13.67 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Spectra
Pathways
Pathways
Protein Targets
EnzymesNot Available
TransportersNot Available
Metal BindingsNot Available
ReceptorsNot Available
Transcriptional FactorsNot Available
Concentrations Data
Not Available
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID29394359
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound71700037
PDB IDNot Available
ChEBI IDNot Available
References
General ReferencesNot Available