Inhibition of SCD in human NCI-H2122 cells expressing CYP4F11 assessed as reduction in cell viability incubated for 96 hrs by cell titer Glo reagent based assay
Inhibition of SCD in human H2009 cells non-expressing CYP4F11 assessed as reduction in cell viability incubated for 96 hrs by cell titer Glo reagent based assay
Inhibition of SCD in human H1819 cells non-expressing CYP4F11 assessed as reduction in cell viability incubated for 96 hrs by cell titer Glo reagent based assay
Drug metabolism in human NCI-H2122 cells assessed as (R)-4-(amino(phenyl)methyl)-N-(6-hydroxybenzo[d]thiazol-2-yl)-benzamide formation at 100 nM by LC-MS/MS analysis
Drug metabolism in human NCI-H1155 cells assessed as (R)-4-(amino(phenyl)methyl)-N-(6-hydroxybenzo[d]thiazol-2-yl)-benzamide formation at 100 nM by LC-MS/MS analysis
Drug metabolism in human NCI-H2122 cells assessed as (R)-4-(amino(phenyl)methyl)-N-(6-hydroxybenzo[d]thiazol-2-yl)-benzamide formation at 100 nM by in presence of CYP4F inhibitor HET0016 LC-MS/MS analysis
Inhibition of SCD in human NCI-H1155 cells non-expressing CYP4F11 assessed as reduction in cell viability incubated for 96 hrs by cell titer Glo reagent based assay
Drug level in plasma of normal chow diet fed nod-SCID mouse xenografted with NCI-H2122 cells at 20 mg/kg, ip QD for 3 weeks and measured 3 hrs after final dose by LC-MS/MS analysis
Drug level in tumor of normal chow diet fed nod-SCID mouse xenografted with NCI-H2122 cells at 20 mg/kg, ip QD for 3 weeks and measured 3 hrs after final dose by LC-MS/MS analysis
Drug level in plasma of fat-free diet fed nod-SCID mouse xenografted with NCI-H2122 cells at 20 mg/kg, ip QD for 3 weeks and measured 3 hrs after final dose by LC-MS/MS analysis
Drug level in tumor of fat-free diet fed nod-SCID mouse xenografted with NCI-H2122 cells at 20 mg/kg, ip QD for 3 weeks and measured 3 hrs after final dose by LC-MS/MS analysis