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. 2017 Nov 21;33(1):58–66. doi: 10.1080/14756366.2017.1389921

Table 1.

Results of pim-1 kinase inhibition achieved by the test compounds.

Inline graphic
Compound number R or Ar % Inhibition at 25µM IC50 (µM)
3a 4-C6H5CH2OC6H4 83 0.96
3b 4-BrC6H4 96 0.06
3c 4-ClC6H4 92 0.14
3d 2,4-(OH)2C6H3 81 1.34
3e 3,4-(OH)2C6H3 93 0.06
3f 4-FC6H4 89 1.00
3g 3-OCH3-4-OHC6H3 92 0.08
3h 4-OCH3C6H4 84 1.17
3i 3,4,5-(OCH3)3C6H2 81 0.93
3j 3-Thienyl 95 0.10
6 H 81 1.08
7a CH3 76 1.76
7b CF3 93 0.08
8 CH2COOC2H5 95 0.10
9a 4-BrC6H4 88 0.52
9b 2-CF3C6H4 89 0.22
Staurosporine 94 Not determined