Inhibition Assay: Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.3%) are incubated with human live...

Basic Information

ID: ALA3888370

Type: Binding

Description: Inhibition Assay: Six test compound concentrations (0.1, 0.25, 1, 2.5, 10, 25 μM in DMSO; final DMSO concentration=0.3%) are incubated with human liver microsomes (0.1 mg/mL) and NADPH (1 mM) in the presence of the probe substrate bupropion (110 μM) for 5 min at 37° C. The selective CYP2B6 inhibitor, ticlopidine, is screened alongside the test compounds as a positive control.

Format: BAO_0000221

Tissue: Liver

Target:  Cytochrome P450 2B6(ALA4729)

Document:  ALA3886683

BindingDB Source:  7942

Activity Charts

Compound Summary

Parent Molecular WeightALogPPolar Surface Area
255.752.272.27