Abstract
Background: A series of 6, 6'-(1,4-phenylene) bis(4-(4-bromophenyl) pyrimidin-2-amine) derivatives has been synthesized by Claisen-Schmidt condensation and its chemical structures was confirmed by FT-IR, H-1/C-13-NMR spectral and elemental analyses. The molecular docking study was carried out to find the interaction between active bis-pyrimidine compounds with CDK-8 protein. The in vitro antimicrobial potential of the synthesized compounds was determined against Gram-positive and Gram-negative bacterial species as well fungal species by tube dilution technique. Antimicrobial results indicated that compound 11y was found to be most potent one against E. coli (MICec = 0.67 mu mol/mL) and C. albicans (MICca = 0.17 mu mol/mL) and its activity was comparable to norfloxacin (MIC = 0.47 mu mol/mL) and fluconazole (MIC = 0.50 mu mol/mL), respectively.
Conclusion: Anticancer screening of the synthesized compounds using Sulforhodamine B (SRB) assay demonstrated that compounds 2y (IC50 = 0.01 mu mol/mL) and 4y (IC50= 0.02 mu mol/mL) have high antiproliferative potential against human colorectal carcinoma cancer cell line than the reference drug (5-fluorouracil) and these compounds also showed best dock score with better potency within the ATP binding pocket and may also be used lead for rational drug designing.