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. 2013 Feb;57(2):1025–1034. doi: 10.1128/AAC.02133-12

Table 1.

Enhancement of drug resistance in the V656L mutant is independent of substrate strength

Compound WT/Δpdr5 IC50 ratio IC50 (μM)
V656L mutant/WT IC50 ratio ATPase IC50 (μM)
WT V656L mutant
Tamoxifen 1.7 13 18 1.4 Incomplete
Cyprodinil 2.0 140 140 1.0 200
Cerulenin 10 14 28 2.0 No inhibition
Imazalil 10 4.3 7.7 1.8 Incomplete
Cycloheximide 17 7.5 16 2.1 No inhibition
Bifonazole 19 3.7 5.7 1.5 5.3
Climbazole 40 14 28 2.0 Incomplete
Clotrimazole 75 9.7 9.7 1.0 2.5
Tebuconazole 80 6.2 9.5 1.5 No inhibition
Cyproconazole 106 7.5 15 2.0 No inhibition