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. Author manuscript; available in PMC: 2013 Sep 1.
Published in final edited form as: Drug Metab Lett. 2012 Sep 1;6(3):157–164. doi: 10.2174/1872312811206030002

Table 2.

Pearson Correlation Values Between R- and S-hydroxywarfarin Formation Rates and P450 Activities as Measured with a Bank of Nine Human Liver Microsomal Samples (See Figs. 3 and 4)a, b

P450
isoform
Probe Drug 6-Hydroxywarfarin 7-Hydroxywarfarin 8-Hydroxywarfarin 10-Hydroxywarfarin 4′-Hydroxywarfarin
R value P value R value P value R value P value R value P value R value P value
CYP1A2 PHEN R-WAR
S-WAR
0.66
0.66
0.056
0.054
0.67
0.50
0.049*
0.17
0.45
0.16
0.22
0.67
0.40
0.063
0.29
0.87
−0.44
−0.023
0.24
0.95
CYP2C19 MEPH R-WAR
S-WAR
0.91
0.37
0.0006***
0.32
0.82
0.28
0.0069**
0.46
0.90
−0.045
0.0009***
0.91
−0.020
−0.98
0.96
0.80
−0.50
−0.46
0.17
0.22
a

PHEN, phenacetin; MEPH, S-mephenytoin; WAR, warfarin

b

Asterisks indicate statistically significant correlations