Record Information
Version1.0
Created at2020-03-19 00:36:57 UTC
Updated at2020-11-18 16:35:10 UTC
CannabisDB IDCDB000438
Secondary Accession NumbersNot Available
Cannabis Compound Identification
Common NameCannabitriolvarin
DescriptionCannabitriolvarin (CBTV) is the C3 analogue of cannabitriol (CBT). CBTV has been reported very scarcely in the literature. Cannabitriolvarin, also belongs to the class of cannabis compounds known as Cannabitriol. CBTV shares the same basic skeleton of tetrahydrocannabivarin (THCV) with the addition of two hydroxil groups and the isomerization of a double bond on the isoprenoid moiety. Little experimental data has been published in regards to the biological activities of CBTV. It has been proposed that CBTV is an intermediate in the aromatization of THCV to cannabivarin (CBV) (PMID: 27722705 ). Cannabitriolvarin has been described as one of the cannabinoids isolated from Cannabis sativa plants (PMID: 6991645 ).
Structure
Thumb
SynonymsNot Available
Chemical FormulaC19H26O3
Average Molecular Weight302.41
Monoisotopic Molecular Weight302.1882
IUPAC Name(9R)-6,6,9-trimethyl-3-propyl-6H,7H,8H,9H,10H-cyclohexa[c]chromene-1,9-diol
Traditional Name(9R)-6,6,9-trimethyl-3-propyl-7H,8H,10H-cyclohexa[c]chromene-1,9-diol
CAS Registry NumberNot Available
SMILES
CCCC1=CC2=C(C(O)=C1)C1=C(CC[C@@](C)(O)C1)C(C)(C)O2
InChI Identifier
InChI=1S/C19H26O3/c1-5-6-12-9-15(20)17-13-11-19(4,21)8-7-14(13)18(2,3)22-16(17)10-12/h9-10,20-21H,5-8,11H2,1-4H3/t19-/m1/s1
InChI KeySWBMWFGNFZCROR-LJQANCHMSA-N
Chemical Taxonomy
ClassificationNot classified
Ontology
Not 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
logP4.13ALOGPS
logP3.83ChemAxon
logS-4ALOGPS
pKa (Strongest Acidic)9.36ChemAxon
pKa (Strongest Basic)-2.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area49.69 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity88.95 m³·mol⁻¹ChemAxon
Polarizability35.35 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
EI-MS/GC-MS
TypeDescriptionSplash KeyView
Predicted GC-MSCannabitriolvarin, 1 TMS, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
Predicted GC-MSCannabitriolvarin, 1 TMS, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
Predicted GC-MSCannabitriolvarin, 2 TMS, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
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 CompoundNot Available
PDB IDNot Available
ChEBI IDNot Available
References
General References
  1. Turner CE, Elsohly MA, Boeren EG: Constituents of Cannabis sativa L. XVII. A review of the natural constituents. J Nat Prod. 1980 Mar-Apr;43(2):169-234. doi: 10.1021/np50008a001. [PubMed:6991645 ]
  2. Hanus LO, Meyer SM, Munoz E, Taglialatela-Scafati O, Appendino G: Phytocannabinoids: a unified critical inventory. Nat Prod Rep. 2016 Nov 23;33(12):1357-1392. doi: 10.1039/c6np00074f. [PubMed:27722705 ]