Research Article
Synthesis, Anticancer Assessment, and Molecular Docking of Novel Chalcone-Thienopyrimidine Derivatives in HepG2 and MCF-7 Cell Lines
Figure 3
Cytotoxicity for some newly synthesized thienopyrimidine derivatives 3a-g against (a) HepG2 and (b) MCF-7 cancer cell lines in comparison to the traditional anticancer drug 5-FU. IC50 of triplicates was expressed as μM.
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