Abstract
Tetrahydropyran derivative 1 was discovered in a high-throughput screening campaign to find new inhibitors of mycobacterial InhA. Following initial in-vitro profiling, a structure-activity relationship study was initiated and a focused library of analogs was synthesized and evaluated. This yielded compound 42 with improved antimycobacterial activity and low cytotoxicity. Additionally, the crystal structure of InhA in complex with inhibitor 1 was resolved, to reveal the binding mode and provide hints for further optimization.
Keywords:
InhA; Inhibitors; Synthesis; Tuberculosis.
Copyright © 2016 Elsevier Masson SAS. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antitubercular Agents / chemistry*
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Antitubercular Agents / pharmacology*
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Bacterial Proteins / antagonists & inhibitors*
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Bacterial Proteins / chemistry
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Bacterial Proteins / metabolism
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Humans
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Microbial Sensitivity Tests
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Models, Molecular
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Mycobacterium tuberculosis / chemistry
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Mycobacterium tuberculosis / drug effects*
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Mycobacterium tuberculosis / metabolism
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Oxidoreductases / antagonists & inhibitors*
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Oxidoreductases / chemistry
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Oxidoreductases / metabolism
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Pyrans / chemistry*
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Pyrans / pharmacology*
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Structure-Activity Relationship
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Tuberculosis / drug therapy
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Tuberculosis / microbiology
Substances
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Antitubercular Agents
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Bacterial Proteins
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Pyrans
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Oxidoreductases
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InhA protein, Mycobacterium