Structure

InChI Key ZROLHBHDLIHEMS-HUUCEWRRSA-N
Smiles CCCc1cc(O)c2c(c1)OC(C)(C)[C@@H]1CCC(C)=C[C@@H]21
InChI
InChI=1S/C19H26O2/c1-5-6-13-10-16(20)18-14-9-12(2)7-8-15(14)19(3,4)21-17(18)11-13/h9-11,14-15,20H,5-8H2,1-4H3/t14-,15-/m1/s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C19H26O2
Molecular Weight 286.42
AlogP 4.96
Hydrogen Bond Acceptor 2.0
Hydrogen Bond Donor 1.0
Number of Rotational Bond 2.0
Polar Surface Area 29.46
Molecular species NEUTRAL
Aromatic Rings 1.0
Heavy Atoms 21.0
Assay Description Organism Bioactivity Reference
Binding affinity to human CB1 receptor Homo sapiens 75.4 nM
Displacement of [3H]-CP55940 from CB1 receptor in mouse whole brain membrane measured after 60 mins by liquid scintillation counting method Mus musculus 75.4 nM
Displacement of [3H]-CP55940 from recombinant human CB2 receptor expressed in CHO cell membranes measured after 60 mins by liquid scintillation counting method Homo sapiens 63.0 nM
Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes after 90 mins Homo sapiens 13.1 nM Displacement of [3H]-CP-55,940 from recombinant human CB1R expressed in HEK293 cell membranes after 90 mins Homo sapiens 1.5 nM
Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes after 90 mins Homo sapiens 17.6 nM Displacement of [3H]-CP-55,940 from recombinant human CB2R expressed in HEK293 cell membranes after 90 mins Homo sapiens 2.8 nM
Inhibition of human LDHB assessed as reduction in lactate production using pyruvate as substrate at 10 uM in presence of NADH by spectrophotometric analysis relative to control Homo sapiens 50.0 %

Related Entries

Cross References

Resources Reference
ChEMBL CHEMBL2387541
DrugBank DB11755
FDA SRS I5YE3I47D8
Guide to Pharmacology 6418
PubChem 93147
SureChEMBL SCHEMBL6856739
ZINC ZINC000005649505