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. 2013 Mar;57(3):1352–1360. doi: 10.1128/AAC.02067-12

Table 1.

Binding parameters for medical azoles with CaCYP51, Δ60HsCYP51, and HsCYP51a

Medical azole antifungal CaCYP51
Δ60HsCYP51
HsCYP51
Fold difference in Kd
Kd (nM) ΔAmax Kd (nM) ΔAmax Kd (nM) ΔAmax Δ60HsCYP51/CaCYP51 HsCYP51/CaCYP51
Clotrimazole 26 ± 6 0.0615 ± 0.0015 55 ± 5 0.0964 ± 0.0028 65 ± 19 0.1091 ± 0.0069 2.1 2.5
Fluconazole 56 ± 4 0.0595 ± 0.0016 30,400 ± 4,100 0.0144 ± 0.0006 30,500 ± 7,700 0.0299 ± 0.0047 543 545
Itraconazole 19 ± 5 0.0493 ± 0.0014 92 ± 7 0.0533 ± 0.0048 131 ± 13 0.0707 ± 0.0036 4.8 6.9
Ketoconazole 12 ± 3 0.1073 ± 0.0019 42 ± 16 0.1315 ± 0.0063 61 ± 17 0.1284 ± 0.0081 3.5 5.1
Voriconazole 10 ± 2 0.0590 ± 0.0032 2,290 ± 120 0.0775 ± 0.0021 2,240 ± 520 0.0480 ± 0.0031 229 224
a

CYP51 concentrations of 5 μM were used. A rearrangement of the Morrison equation was used to determine Kd values for the ligands with tight binding (40). Mean Kd and ΔAmax values of three replicates are shown with the associated standard deviations.