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Title: Novel pyrazole derivatives as potent inhibitors of type II topoisomerases. Part 1: synthesis and preliminary SAR analysis. Author: Gomez L, Hack MD, Wu J, Wiener JJ, Venkatesan H, Santillán A, Pippel DJ, Mani N, Morrow BJ, Motley ST, Shaw KJ, Wolin R, Grice CA, Jones TK. Journal: Bioorg Med Chem Lett; 2007 May 15; 17(10):2723-7. PubMed ID: 17368897. Abstract: In an attempt to search for a new class of antibacterial agents, we have discovered a series of pyrazole analogs that possess good antibacterial activity for Gram-positive and Gram-negative organisms via inhibition of type II bacterial topoisomerases. We have investigated the structure-activity relationships of this series, with an emphasis on the length and conformation of the linker. This work led to the identification of tetrahydroindazole analogs, such as compound 1, as the most potent class of compounds.[Abstract] [Full Text] [Related] [New Search]