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. 2017 Aug 31;12(18):1542–1554. doi: 10.1002/cmdc.201700340

Table 4.

Synthesized prodrugs, metabolic stability (based on LC–UV analysis), and effect on PC3 proliferation.[a]

graphic file with name CMDC-12-1542-g016.jpg
Compd R Residual microsomal substrate [%] (t=60 min) Mouse plasma t 1/2 [min] Cell proliferation
64 Me 20 13.3 active
65 Bn 53 <1 active
66 iPr 16 15.1 active
67 Et 24 4.5 active
68 Bu 53 <1 active
69 tBu 79 N.C. inactive
70 CH2‐pyridin‐4‐yl 0 <1 active
71 (CH2)2‐morpholinyl 18 2.5 active
72 piperonyl 83 <1 active
73 isopentyl 39 <1 active
74 1‐methylbutanyl 60 4.2 inactive
75 (CH2)10Me 80 4.4 inactive
76 (CH2)17Me 100 N.C. inactive

[a] N.C.: not calculable as hydrolytically stable. Active: able to reduce proliferation to an extent greater than 50 %; inactive: able to reduce proliferation to an extent less than 50 %.