A series of spirocyclic analogues as potent inhibitors of bacterial phenylalanyl- t RNA synthetases-Reference-Cited by-同舟云学术

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A series of spirocyclic analogues as potent inhibitors of bacterial phenylalanyl- t RNA synthetases

Published:2004-03 Issue:5 Volume:14 Page:1339-1342
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Yu Xiang Y.,Finn John,Hill Jason M.,Wang Zhong G.,Keith Dennis,Silverman Jared,Oliver N.

Publisher

Elsevier BV

Subject

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

Reference24 articles.

1. Antibacterial agents based on the cyclic d,l-α-peptide architecture

2. Importance of antifungal drug-resistance: clinical significance and need for novel therapy

3. -Lactamases of Gram-Negative Bacteria: New Challenges for New Drugs

4. Functional Dissection of a Predicted Class-Defining Motif in a Class II tRNA Synthetase of Unknown Structure

5. The aminoacyl-tRNA synthetase family: Modules at work

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