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Tuberculosis
Scientists at Colorado State University publish new data on tuberculosis
August 12th, 2008
"Previous structure-based design studies resulted in the discovery of alkyl substituted diphenyl ether inhibitors of InhA, the enoyl reductase from Mycobacterium tuberculosis," scientists writing in the journal Bioorganic & Medicinal Chemistry Letters report. "Compounds such as 5-hexyl-2-phenoxyphenol 19 are nM inhibitors of InhA and inhibit the growth of both sensitive and isoniazid-resistant strains of Mycobacterium tuberculosis with MIC90 values of 1-2 mu g/mL. However, despite their promising in vitro activity, these compounds have ClogP values of over 5. In efforts to reduce the lipophilicity of the compounds, and potentially enhance compound...
Source: TB & Outbreaks Week (2008-08-12)
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