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. Author manuscript; available in PMC: 2017 Jul 7.
Published in final edited form as: Eur J Med Chem. 2016 Nov 14;126:502–516. doi: 10.1016/j.ejmech.2016.11.027

Table 1.

Activity of compounds 6a–m and 7a–m against NV 3CL protease and replicon harboring cells.

Compound R IC50 (μM) EC50 (μM) CC50 (μM)
6a C6H5 8.5 9.5 > 100
7a 13.5 12.3 > 100

6b (C6H5) CH2 4.5 4.1 > 100
7b 4.3 4.3 > 100

6c (C6H5) CH2CH2 1.8 0.7 > 100
7c 2.1 0.8 > 100

6d p-F (C6H4) 4.8 2 > 100
7d 6.2 2.1 > 100

6e m-Cl (C6H4) 5.5 2.3 > 100
7e 5.7 1.9 > 100

6f p-Cl (C6H4) 5.8 3.5 > 100
7f 5.1 7.2 > 100

6g p-Cl (C6H4) CH2 1.8 2.4 > 100
7g 1.2 2.2 > 100

6h m-Cl (C6H4) CH2CH2 2.3 1.1 > 100
7h 1.9 0.8 > 100

6i 2-Thiophene 10.4 8.5 > 100
7i 8.5 8.1 > 100

6j Biphenyl-4- 1.3 1.3 > 100
7j 1.1 1.2 > 100

6k 2-Phthalimidoethane 2.5 2.3 > 100
7k 2.6 2.1 > 100

6l p-CH3O(C6H4)O(CH2)3 1.8 0.2 > 100
7l 1.6 0.2 > 100

6m CH3(CH2)7 1.2 0.3 33.8
7m 1.1 0.2 35.4