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. 2011 May;55(5):1975–1981. doi: 10.1128/AAC.01627-10

Table 3.

Physicochemical parametersa

Cyclophilin inhibitor Solubility (μM) log D, pH 7.4 HLM t1/2 (min) MLM t1/2 (min) Human hepatocyte t1/2 (min)
SfA 45 >4.6 7.9 4.0 145
SfB 16 >4.5 7.0 2.4 156
SfC 10 >4.2 3.4 11.0 40
SfD 25 4.1 4.4 9.1 54
a

Data are shown for solubility in PBS (pH 7.4), lipophilicity (log D, pH 7.4), and human (HLM) and mouse (MLM) microsome and hepatocyte stability (t1/2).