Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1378239 | Bioorganic & Medicinal Chemistry Letters | 2007 | 8 Pages |
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.
Related Topics
Physical Sciences and Engineering
Chemistry
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Authors
Rameshwar U. Kadam, Archana Chavan, Nilanjan Roy,