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Synthesis of 4-amino-5-cyano-2, 6-Disubstituted Pyrimidines as a Potential Antifilarial DNA Topoisomerase II Inhibitors

[ Vol. 4 , Issue. 6 ]


Ashok Kumar, J. K. Saxena and Prem M.S. Chauhan   Pages 577 - 585 ( 9 )


A novel series of 4-amino-5-cyano-2, 6-disubstituted pyrimidines have been synthesized and evaluated for their in vitro antifilarial DNA topoisomerase II activity against filarial parasite Setaria Cervi. In particular compounds bearing 4-chloro-phenyl substitutent at position-6, exhibited strong inhibition at 40 μg/mL and 5 μg/mL concentration. The present study based on the biological results obtained, suggests that the nature of substitutent at position-4 in the phenyl ring directly affects DNA topoisomerase II inhibitory activity. Most of the compounds have shown better topoisomerase II inhibitory activity than the standard antifilarial drug (DEC) and the topoisomerase II inhibitors (Novobiocin, Nalidixic acid).


Pyrimidine, antifilarial, topoisomerase II, knoevenagel condensation


Medicinal and Process Chemistry Division, Central Drug Research Institute, Lucknow 226001, India.

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