Inhibition of Siderophore Biosynthesis by 2-Triazole Substituted Analogues of 5′-O-[N-(Salicyl)sulfamoyl]adenosine: Antibacterial Nucleosides Effective against Mycobacterium tuberculosis-Reference-Cited by-同舟云学术

Inhibition of Siderophore Biosynthesis by 2-Triazole Substituted Analogues of 5′-O-[N-(Salicyl)sulfamoyl]adenosine: Antibacterial Nucleosides Effective against Mycobacterium tuberculosis

Published:2008-11-14 Issue:23 Volume:51 Page:7495-7507
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Gupte Amol¹,Boshoff Helena I.¹,Wilson Daniel J.¹,Neres João¹,Labello Nicholas P.¹,Somu Ravindranadh V.¹,Xing Chengguo¹,Barry Clifton E.¹,Aldrich Courtney C.¹

Affiliation:

1. Center for Drug Design, Academic Health Center, University of Minnesota, Minneapolis, Minnesota 55455, Tuberculosis Research Section, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892, and Department of Medicinal Chemistry, University of Minnesota, Minneapolis, Minnesota 55455

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm8008037

Reference42 articles.

1. Prospects for new antitubercular drugs

2. Natural Products, Small Molecules, and Genetics in Tuberculosis Drug Development

3. Enterobactin: An archetype for microbial iron transport

4. Iron Metabolism in Pathogenic Bacteria

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