Structure based design of an in vivo active hydroxamic acid inhibitor of P. aeruginosa LpxC-Reference-Cited by-同舟云学术

Structure based design of an in vivo active hydroxamic acid inhibitor of P. aeruginosa LpxC

Published:2012-04 Issue:7 Volume:22 Page:2536-2543
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Warmus Joseph S.,Quinn Cheryl L.,Taylor Clarke,Murphy Sean T.,Johnson Timothy A.,Limberakis Chris,Ortwine Daniel,Bronstein Joel,Pagano Paul,Knafels John D.,Lightle Sandra,Mochalkin Igor,Brideau Roger,Podoll Terry

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference25 articles.

1. Bad Bugs, No Drugs: No ESKAPE! An Update from the Infectious Diseases Society of America

2. Recognition and prevention of multidrug-resistant Gram-negative bacteria in the intensive care unit

3. Outcome of infections due to pandrug-resistant (PDR) Gram-negative bacteria

4. α,β-Cyclic-β-benzamido hydroxamic acids: Novel oxaspiro[4.4]nonane templates for the discovery of potent, selective, orally bioavailable inhibitors of tumor necrosis factor-α converting enzyme (TACE)

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