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. 2023 Dec 14;28(24):8095. doi: 10.3390/molecules28248095

Table 2.

In vitro antiproliferative activity of nitrostyrene compounds 11g, 11h, 11i and 11j in HeLa, MCF-7, HL-60, Ramos, Bjab, MUTU-I and DG-75 cell lines a.

graphic file with name molecules-28-08095-i001.jpg

% Viable Cells Remaining
HeLa
24 h
MCF-7
72 h
Ramos
24 h
Bjab
24 h
HL60
24 h
MUTU-1 b
24 h
DG-75 b
48 h
10
µM
1
µM
10
µM
1
µM
10
µM
1
µM
10
µM
1
µM
10
µM
1
µM
10
µM
1
µM
10
µM
1
µM
11g 34.2 87.1 41.7 81.4 7.7 53.4 51.9 82.2 16.5 73.4 14.91 44.16 −0.08 75.86
11h 23.2 90.6 29.7 94.3 5.1 27.2 46.2 90.1 6.8 78.2 10.28 39.80 0.38 84.50
11i 17.7 93.0 37.1 102.7 13.9 62.6 50.8 100.5 6.5 103.8 10.53 67.22 0.72 88.76
11j 21.8 95.3 20.7 98.1 4.4 66.9 68.9 102.4 9.1 99.8 10.27 64.31 15.89 79.77
Taxol 48.4 86.9 75.0 100.8 24.9 69.3 80.2 97.6 69.7 97.6 7.0 32.0 40.0 >90

a Cell proliferation of HeLa, MCF-7, HL-60, Ramos, Bjab, MUTU-I and DG-75 cells was determined with an alamarBlue assay. Compound concentrations of either 1 μM or 10 μM for 24 h (HeLa, Ramos, Bjab, HL60 and MUTU-I) or 48 h (DG-75) or 72 h (MCF-7) were used to treat the cells (in triplicate) with control wells containing vehicle ethanol (1% v/v). The mean value for three independent experiments is shown b [39].