Design and chemical behavior of novel pyrimidine derivatives and their evaluation of cytotoxicity

Faculty Science Year: 2020
Type of Publication: ZU Hosted Pages: Pages 1232-1238
Authors:
Journal: Synthetic Communications An International Journal for Rapid Communication of Synthetic Organic Chemistry Taylor and Francis Group Volume:
Keywords : Design , chemical behavior , novel pyrimidine derivatives    
Abstract:
Diphenyl-4-thioxo-1,4-dihydropyrimidin-5-yl)ethan-1-one 4 was obtained upon the reaction of (phenylamino)but-2-enethioyl)benzamide 3 with sodium hydroxide. The reactions of 4 with several active species such as benzaldehyde, urea, malononitrile, ethyl cyanoacetate, hydrazine, and carbon disulfide were studied. The antitumor activities of some selective compounds were examined against two cell lines: Mammalian cell lines: A-549 cells (human lung cancer cell line) and MRC-5 cells (normal human lung fibroblast cell line); some of the compounds were highly efficient; compound 13 has the most effective anticancer activity.
   
     
 
       

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