Journal of Medicinal Chemistry · 2018 · 145 citations · 115 references
PharmacyBiochemistryMedicinal ChemistryDrug DesignDrug DiscoveryEnzymologyAntibacterial AgentsEnzyme InhibitionTuberculosis PharmacotherapyBacterial Cell Wall Synthesis InhibitorsCatalytic ActivityCell Wall Polysaccharide SynthesisCell Wall Synthesis InhibitionDruggable Target DiscoveryHigh-throughput Screening AssaysTuberculosis Drug DevelopmentTuberculosis Drug Resistance
Decaprenylphosphoryl-β-d-ribose 2'-epimerase (DprE1), a vital enzyme for cell wall synthesis, plays a crucial role in the formation of lipoarabinomannan and arabinogalactan. It was first reported as a druggable target on the basis of inhibitors discovered in high throughput screening of a drug library. Since then, inhibitors with different types of chemical scaffolds have been reported for their activity against this enzyme. Formation of a covalent or noncovalent bond by the interacting ligand with the enzyme causes loss of its catalytic activity which ultimately leads to the death of the mycobacterium. This Perspective describes various DprE1 inhibitors as anti-TB agents reported to date.
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