alexa Substituted quinolinyl chalcones and quinolinyl pyrimidines as a new class of anti-infective agents.
Chemistry

Chemistry

Chemical Sciences Journal

Author(s): Sharma M, Chaturvedi V, Manju YK, Bhatnagar S, Srivastava K,

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Abstract Frequency of tuberculosis and malaria is progressively increasing worldwide. New emerging strain of bacterium and resistance to currently available drugs make this field more conscientious and alarming. In this connection a series of substituted quinolinyl chalcones and substituted quinolinyl pyrimidines were synthesized and evaluated for their in vitro antitubercular activity against Mycobacterium tuberculosis H(37)R(V) and antimalarial activity against NF-54 strain of Plasmodium falciparum. A comparison of structure-activity relationship reveals that different physicochemical and structural requirements exist for these two activities. Out of synthesized compounds, compound nos. 22 and 23 have shown antitubercular activity of MIC 3.12 microg/mL and were nontoxic against VERO, MBMDM cell lines and compounds 54, 55, and 56 have shown antimalarial activity of MIC 1 microg/mL. This article was published in Eur J Med Chem and referenced in Chemical Sciences Journal

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