Record Information
Version1.0
Created at2020-04-27 16:49:53 UTC
Updated at2021-01-04 18:49:11 UTC
CannabisDB IDCDB005729
Secondary Accession NumbersNot Available
Cannabis Compound Identification
Common Name3,5,7-Trimethyl-1,6-naphthyridine
Description3,5,7-Trimethyl-1,6-naphthyridine or 3,5,7-trimethyl-1,6-diazanaphthalene is a trimethylated derivative of 1,6-naphthyridine. It belongs to the class of organic compounds known as naphthyridines. Naphthyridines are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom. 3,5,7-trimethyl-1,6-naphthyridine is one of several structural isomers of trimethylnaphthyridine wherein three methyl groups are substituted at different positions of naphthyridine. Trimethylnaphthyridines are found in cannabis smoke. 3,5,7-Trimethyl-1,6-naphthyridine is formed during the combustion of cannabis ( Ref:DOI ).
Structure
Thumb
SynonymsNot Available
Chemical FormulaC11H12N2
Average Molecular Weight172.23
Monoisotopic Molecular Weight172.1
IUPAC Name3,5,7-trimethyl-1,6-naphthyridine
Traditional Name3,5,7-trimethyl-1,6-naphthyridine
CAS Registry NumberNot Available
SMILES
CC1=CC2=C(C)N=C(C)C=C2N=C1
InChI Identifier
InChI=1S/C11H12N2/c1-7-4-10-9(3)13-8(2)5-11(10)12-6-7/h4-6H,1-3H3
InChI KeyPMWLKVFAHRPRED-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as naphthyridines. Naphthyridines are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassDiazanaphthalenes
Sub ClassNaphthyridines
Direct ParentNaphthyridines
Alternative Parents
Substituents
  • Naphthyridine
  • Methylpyridine
  • Pyridine
  • Heteroaromatic compound
  • Azacycle
  • Organic nitrogen compound
  • Organopnictogen compound
  • Hydrocarbon derivative
  • Organonitrogen compound
  • 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
logP2.36ALOGPS
logP1.69ChemAxon
logS-2.8ALOGPS
pKa (Strongest Basic)4.49ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area25.78 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity52.05 m³·mol⁻¹ChemAxon
Polarizability19.85 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Spectra
EI-MS/GC-MSNot Available
MS/MS
TypeDescriptionSplash KeyView
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, PositiveNot Available2020-06-30View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, PositiveNot Available2020-06-30View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, PositiveNot Available2020-06-30View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, NegativeNot Available2020-06-30View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, NegativeNot Available2020-06-30View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, NegativeNot Available2020-06-30View Spectrum
NMRNot Available
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 IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound143030619
PDB IDNot Available
ChEBI IDNot Available
References
General ReferencesNot Available