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. Author manuscript; available in PMC: 2019 Jan 1.
Published in final edited form as: Eur J Med Chem. 2017 Nov 4;143:1919–1930. doi: 10.1016/j.ejmech.2017.11.006

Table 2.

In vitro anti-proliferative activities of N1-monosubstituted and N1,N3-disubstituted thiobarbituric acid derivatives on melanoma CHL-1 and UACC 903 cancer cells (72 h treatment).a

Compounds Melanoma cells IC50 (μM)
CHL-1 UACC 903
8a 7.5 ± 1.7 6.7 ± 1.2
8b 3.8 ± 1.3 3.8 ± 0.4
8c 4.7 ± 0.5 5.5 ± 1.9
8d 13.9 ± 2.3 16.2 ± 3.0
8e 4.7 ± 1.1 4.6 ± 0.9
8f 6.2 ± 2.2 8.0 ± 1.8
8g 23.4 ± 1.7 23.4 ± 3.6
8h 7.5 ± 2.8 7.6 ± 3.9
8i 8.6 ± 1.9 18.8 ± 2.7
8j 8.8 ± 3.1 15.2 ± 2.3
8k 18.9 ± 2.8 14.5 ± 1.7
8l 20.4 ± 3.7 21.0 ± 3.6
8m 6.1 ± 2.1 6.1 ± 1.4
8n 8.0 ± 2.9 17.6 ± 2.9
8o 8.1 ± 0.7 18.1 ± 3.2
PLX-4032 13.7 ± 1.7 3.6 ± 1.1
a

Values are the mean of triplicates of at least two independent experiments. Non-linear graphs using Prism software were used to determine Mean ± SD values.