Research Article

Synthesis and In Vitro Cytotoxic Activity of Chromenopyridones

Table 2

IC50 (μM) of synthesized compounds against various human cancer cell lines.

Compound numberIC50 ± SE* in μM
PC-3
(Prostate)
MCF-7
(Breast)
IMR-32
(CNS)
Hela
(Cervix)
Hep-G2
(Liver)

3a82.4 ± 3.590.6 ± 2.580.4 ± 3.5>100>100
3b79.2 ± 3.580.2 ± 3>100>10090.6 ± 2.5
3c88.9 ± 2.3>10090.4 ± 3.588.8 ± 1.3>100
3d78.2 ± 2.486.2 ± 3.577.4 ± 3.5>10083.5 ± 1.2
3e81.9 ± 2.683.2 ± 1.593.2 ± 2.5>100>100
3f28.7 ± 3.339.6 ± 3.523.9 ± 2.815.7 ± 3.5>100
3g21.5 ± 2.523.8 ± 3.219.2 ± 2.320.4 ± 1.544.1 ± 2.1
3h41.9 ± 3.515.5 ± 2.3>10028.7 ± 1.585.6 ± 2.2
3i80.3 ± 1.354.6 ± 3.833.7 ± 1.221.8 ± 3.554.2 ± 2.6
3j54.2 ± 2.533.4 ± 1.219.2 ± 2.588.2 ± 3.238.9 ± 1.1
6a19.5 ± 2.4>10033.5 ± 3.336.1 ± 2.144.9 ± 3.2
6b2.4 ± 3.410.7 ± 2.513.2 ± 2.37.0 ± 3.516.3 ± 3.5
6c13.4 ± 1.111.0 ± 2.315.6 ± 2.141.9 ± 3.523.6 ± 2.5
6d14.1 ± 2.214.6 ± 1.516.3 ± 1.4>10041.0 ± 2.3

Paclitaxel0.2 ± 0.03
5-Fluorouracil1.3 ± 0.010.5 ± 0.05
Mitomycin-C1.5 ± 0.022.0 ± 0.03

*Standard error (±).