Skip to main content

Table 1 List of Methylisatin-β-thiosemicarbazone (MIBT) derivatives and the CC50 on PS and BHK-21 cells

From: N-methylisatin-beta-thiosemicarbazone derivative (SCH 16) is an inhibitor of Japanese encephalitis virus infection in vitro and in vivo

Compounds

*CC50 on PS cell line

*CC50 on BHK-21 cell line

1 SF3

47 μg/ml

86 ug/ml

2 SF7

43 μg/ml

200 ug/ml

3 SCH16

76 μg/ml

126 ug/ml

4 SF17

21 μg/ml

42 ug/ml

5 SCH17

41 μg/ml

46 ug/ml

6 SC18

17 μg/ml

82 ug/ml

7 SCH19

18 μg/ml

141 ug/ml

8 SC18

31.5 μg/ml

140 ug/ml

9 SB18

22.5 ug/ml

36 ug/ml

10 SF24

25.5 ug/ml

16.8 ug/ml

11 SF27

22.5 ug/ml

51 ug/ml

12 SC27

21 ug/ml

46 ug/ml

13 SC28

21 ug/ml

94 ug/ml

14 SB29

25 ug/ml

21.5 ug/ml

15.Ribavirin

50 ug/ml

200 ug/ml

  1. *CC50 = The concentration of the compound that reduced the viability of cells to 50% of the control. Note: The 14 MIBT compounds belonged to four different categories based on the halogen or methyl group substituted at the position R and are designated as SB group with bromine, SC group with chlorine, SF group with fluorine and SCH group with -CH3 group substituted at R. R' has N-substituted aromatic side chain attached to the -CH2 moiety. Cytotoxicity concentration (CC50) of synthesized compounds was evaluated on exponentially growing PS and BHK-21 cells. It can be observed that the CC50 of MIBT derivatives ranged from ≥ 76 ug/ml to ≥ 17 ug/ml, while CC50 on BHK-21 cell line ranged from ≥ 200 ug/ml to ≥ 16.8 ug/ml.