Article ID Journal Published Year Pages File Type
1378239 Bioorganic & Medicinal Chemistry Letters 2007 8 Pages PDF
Abstract
An electronic and structural analysis of Pseudomonas aeruginosa Deacetylase LpxC inhibitors reveals characteristic pharmacophoric features of these inhibitors, which are useful for in-depth understanding of inhibitors-enzyme interaction and designing more potent inhibitors against this target.
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Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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