TABLE 1

MRM transitions and major P450 isoforms responsible for metabolism of the 17 test compounds

CompoundMRM Transition (± mode)P450 IsoformHLM KmReferences for Km Values
μM
Riluzole235-166(+)CYP1A230Sanderink et al., 1997
Theophylline181-124(+)4.5Sarkar et al., 1990
Lidocaine235-86 (+)1500Wang et al., 1999a
Diclofenac298-252(+)CYP2C922Carlile et al., 1999
Glimepiride489-364(−)0.56Maekawa et al., 2009
Meloxicam352-184(+)14Chesné et al., 1998
Tolbutamide273-155(+)14Carlile et al., 1999
Warfarin307-250(-)0.29Ngui et al., 2001
Voriconazole350-281(+)CYP2C198.1Hyland et al., 2003
Diazepam285-193(+)180Andersson et al., 1994
Flecainide415-301(+)CYP2D6UnknownNot available
Risperidone411-191(+)0.26Yasui-Furukori et al., 2001
Atomoxetine256-148(+)2.2Ring et al., 2002
Alprazolam309-281(+)CYP3A4340Gorski et al., 1999
Atazanavir705-335(+)UnknownNot available
Midazolam326-291(+)7.5Wang et al., 1999b
Prednisolone361-343(+)UnknownNot available
  • HLM, human liver microsomes; MRM, multiple reaction monitoring.