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. Author manuscript; available in PMC: 2016 Jan 7.
Published in final edited form as: Eur J Med Chem. 2014 Oct 14;89:442–466. doi: 10.1016/j.ejmech.2014.10.034

Table 4.

Anti-proliferative activity manifested by biphenyl derivatives that contain a modified benzylamide side chain.

graphic file with name nihms-639562-t0019.jpg

Entry R SKBr3 (IC50, μM) MCF-7 (IC50, μM)
41a phenyl 4.13±0.22 3.95±0.13
41b 4-chlorophenyl 0.57±0.01 0.52±0.03
41c 4-bromophenyl 0.52±0.21 0.52±0.15
41d 4-iodophenyl 0.31±0.09 0.58±0.01
41e 4-methylphenyl 0.98±0.19 1.27±0.13
41f 4-methoxyphenyl 0.49±0.01 0.65±0.04
41g 4-t-butylphenyl 1.26±0.37 1.08±0.08
41h 3-chlorophenyl 1.94±0.37 2.83±0.69
41i 3 -methoxyphenyl 2.87±0.51 5.31±0.70
41j 3 -methyl -4 -chl orophenyl 1.11±0.42 1.03±0.16
41k 3-chloro-4-methylphenyl 1.96±0.24 2.28±0.49
41l 3 -bromo-4-methylphenyl 2.80±0.18 3.35±0.36
41m 3-iodo-4-methylphenyl 0.93±0.20 1.17±0.20
41n 3,4-dichl orophenyl 1.20±0.08 1.60±0.16
41o 3,5-dichl orophenyl 0.81±0.28 1.68±0.13
41p 2,4-dichlorophenyl 0.80±0.22 1.37±0.33
41q 2-biphenyl 6.26±1.54 6.67±0.83
41r 3-biphenyl 0.73±0.07 1.15±0.18
41s 4-biphenyl 4.59±0.06 4.44±0.60
43a 1-naphthoyl 0.22±0.13 0.58±0.02
43b 2-naphthoyl 0.35±0.02 0.49±0.11
45a 2-quinolinyl 2.42±0.62 2.76±0.76
45b 6-quinolinyl 1.31±0.18 2.07±0.16
47a 2-indolyl 0.64±0.08 0.58±0.02
47b 2-benzo[b]thiophenyl 1.32±0.23 2.01±0.58
8i -- 0.47±0.06 0.71±0.02