Inhibition of human transmembrane domain deficient FFAH expressed in Escherichia coli using AAMCA as substrate incubated for 1 min measured for 50 mins by fluorescence assay
Intrinsic metabolic stability in human liver microsomes assessed as metabolic turnover rate per mg protein at 1 uM preincubated for 5 mins followed by NADPH cofactor addition and measured after 30 mins by LC-MS/MS analysis
Intrinsic metabolic stability in rat liver microsomes assessed as metabolic turnover over per mg protein at 1 uM preincubated for 5 mins followed by NADPH cofactor addition and measured after 30 mins by LC-MS/MS analysis
Inhibition of CYP1A2 in human liver microsomes using phenacetin as substrate preincubated for 5 mins followed by NADPH cofactor addition and measured after 10 mins by LC-MS/MS analysis
Inhibition of CYP2C9 in human liver microsomes using diclofenac as substrate preincubated for 5 mins followed by NADPH cofactor addition and measured after 10 mins by LC-MS/MS analysis
Inhibition of CYP2C19 in human liver microsomes using (S)-mephenytoin as substrate preincubated for 5 mins followed by NADPH cofactor addition and measured after 40 mins by LC-MS/MS analysis
Inhibition of CYP2D6 in human liver microsomes using dextromethorphan as substrate preincubated for 5 mins followed by NADPH cofactor addition and measured after 10 mins by LC-MS/MS analysis
Inhibition of CYP3A4 in human liver microsomes using testosterone as substrate preincubated for 5 mins followed by NADPH cofactor addition and measured after 10 mins by LC-MS/MS analysis
Inhibition of CYP3A4 in human liver microsomes using midazolam as substrate preincubated for 5 mins followed by NADPH cofactor addition and measured after 10 mins by LC-MS/MS analysis
Volume of distribution at steady state in Sprague-Dawley rat at 3 mg/kg, iv or 10 mg/kg, po administered as single dose via gavage by LC-MS/MS analysis