Design and synthesis of 2-pyridones as novel inhibitors of the Bacillus anthracis enoyl-ACP reductase |
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Authors: | Tipparaju Suresh K Joyasawal Sipak Forrester Sara Mulhearn Debbie C Pegan Scott Johnson Michael E Mesecar Andrew D Kozikowski Alan P |
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Institution: | Drug Discovery Program, Department of Medicinal Chemistry and Pharmacognosy, University of Illinois at Chicago, 833 S. Wood Street, Chicago, IL 60612, USA. |
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Abstract: | Enoyl-ACP reductase (ENR), the product of the FabI gene, from Bacillus anthracis (BaENR) is responsible for catalyzing the final step of bacterial fatty acid biosynthesis. A number of novel 2-pyridone derivatives were synthesized and shown to be potent inhibitors of BaENR. |
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