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Bioorganic & Medicinal Chemistry Letters|April 6, 2017
Design, synthesis and optimization of bis-amide derivatives as CSF1R inhibitorsSreekanth A Ramachandran, Pradeep S Jadhavar, Sandeep K Miglani, et al.Antimicrobial Agents and Chemotherapy|April 2, 2014
Assessment of Mycobacterium tuberculosis pantothenate kinase vulnerability through target knockdown and mechanistically diverse inhibitorsB K Kishore Reddy, Sudhir Landge, Sudha Ravishankar, et al.Bioorganic & Medicinal Chemistry Letters|November 15, 2008
Peptide deformylase inhibitors of Mycobacterium tuberculosis: synthesis, structural investigations, and biological resultsArkadius Pichota, Jeyaraj Duraiswamy, Zheng Yin, et al.Antimicrobial Agents and Chemotherapy|October 16, 2013
Optimization of pyrrolamides as mycobacterial GyrB ATPase inhibitors: structure-activity relationship and in vivo efficacy in a mouse model of tuberculosisShahul Hameed P, Suresh Solapure, Kakoli Mukherjee, et al.Journal of Medicinal Chemistry|May 10, 2014
Novel N-linked aminopiperidine-based gyrase inhibitors with improved hERG and in vivo efficacy against Mycobacterium tuberculosisShahul Hameed P, Vikas Patil, Suresh Solapure, et al.Journal of Medicinal Chemistry|June 11, 2014
Aminoazabenzimidazoles, a novel class of orally active antimalarial agentsShahul Hameed P, Murugan Chinnapattu, Gajanan Shanbag, et al.Nature Communications|April 1, 2015
Triaminopyrimidine is a fast-killing and long-acting antimalarial clinical candidateShahul Hameed P, Suresh Solapure, Vikas Patil, et al.Journal of Medicinal Chemistry|January 12, 2017
Discovery of Imidazo[1,2-a]pyridine Ethers and Squaramides as Selective and Potent Inhibitors of Mycobacterial Adenosine Triphosphate (ATP) SynthesisSubramanyam J Tantry, Shankar D Markad, Vikas Shinde, et al.Pageof 2