TABLE 5

Comparison of P450 phenotyping data using rhP450-ISEF extrapolation and HLM chemical inhibition for proprietary compounds

CompoundP450rhP450 CLintHLM CLint-ISEF Extrapolated% Contribution
CalculatedMeasured (HLM with Inhibitor)a
μl per min/pmolμl per min/mg
I2D63.505.046551
2C190.4341.521925
1A20.1411.251624
II3A40.70815.510075
1A2N.D.N.D.12
2C9N.D.N.D.13
III3A40.93220.485100b
2C90.0583.715N.A.
IV3A41.0723.47271
2C90.085.101629
2C191.103.8512N.A.
V3A40.77016.89694
2C190.2190.7746
VI3A42.0244.2100100
VII3A40.78117.19086
2C80.0451.528.1N.A.
2C190.0780.271.414
VIII3A41.06423.39481
1A20.1631.44619
IX3A41.41230.97967
1A20.3182.817.23.4
2C190.5471.914.98.8
2C90.0472.987.79.6
2D60.1930.280.711
X3A40.91219.47780c
1A20.2562.268.914c
2C80.0913.08124.5c
2C190.1570.552.21.7c
  • N.D., not detected; N.A., data not available.

  • a Experimental data normalized to 100%.

  • b Determined on the basis of hydroxylation metabolite formation.

  • c Determined on the basis of one major metabolite formation in 14C-X study.