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. 2025 Aug 22;15(36):29753–29776. doi: 10.1039/d5ra04997k

Table 6. In vitro inhibitory activities of 6b, 7b, 8b, 12a–c, and 13b against CDK6, VEGFR-2 and xanthine oxidase enzymes compared with palbociclib, sorafenib and allopurinol reference compounds, respectively.

Entry pIC50 CDK6 ± SD pIC50 VEGFR-2 ± SD pIC50 XO ± SD
6a 6.22 ± 0.023 6.51 ± 0.012 4.36 ± 0.55
7b 5.82 ± 0.059 6.29 ± 0.02 4.18 ± 0.82
8b 7.17 ± 0.003 7.15 ± 0.003 4.66 ± 0.33
12a 6.81 ± 0.006 7.27 ± 0.002 4.94 ± 0.16
12b 6.91 ± 0.048 6.92 ± 0.006 4.51 ± 0.62
12c 6.93 ± 0.005 6.84 ± 0.009 4.83 ± 0.23
13b 6.09 ± 0.032 6.49 ± 0.012 4.41 ± 0.49
Palbociclib 6.79 ± 0.006
Sorafenib 7.25 ± 0.002
Allopurinol 4.57 ± 0.13