Journal of Enzyme Inhibition and Medicinal Chemistry · 2019 · 35 citations · 20 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryLead OptimizationAntibacterial AgentsAntibacterial PharmacologyAntibacterial TherapyAntibiotic ResistanceEnzyme InhibitionHit-to-lead OptimizationAntibacterial Drug DevelopmentAntibiotic DiscoveryAntimicrobial Drug DevelopmentBinding Mode AnalysisBinding Mode OptimizationNitro CompoundsNovel Antibacterial AgentsNovel Antibacterial Drug Discovery
Starting from the analysis of the hypothetical binding mode of our previous furan-based hit (I), we successfully achieved our objective to replace the nitro moiety, leading to the disclosure of a new lead exhibiting a strong activity against MbtI. Our best candidate 1 h displayed a Ki of 8.8 µM and its antimycobacterial activity (MIC99 = 250 µM) is conceivably related to mycobactin biosynthesis inhibition. These results support the hypothesis that 5-phenylfuran-2-carboxylic derivatives are a promising class of MbtI inhibitors.
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