Design and synthesis of water-soluble prodrugs of rifabutin for intraveneous administration-Reference-Cited by-同舟云学术

Design and synthesis of water-soluble prodrugs of rifabutin for intraveneous administration

Published:2022-08 Issue: Volume:238 Page:114515
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Antraygues Kevin,Maingot Mathieu,Schellhorn Birgit,Trebosc Vincent,Gitzinger Marc,Deprez Benoit,Defert Olivier,Dale Glenn E.,Bourotte Marilyne,Lociuro Sergio,Willand Nicolas^ORCID

Funder

European Regional Development Fund

Conseil Régional Hauts-de-France

European Commission

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference42 articles.

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2. Comparative activity of rifabutin and rifampicin against gram-negative bacteria that have damaged or defective outer membranes;Vaara;J. Antimicrob. Chemother.,1993

3. Rifamycin inhibition of WT and Rif-resistant Mycobacterium tuberculosis and Escherichia coli RNA polymerases in vitro;Gill;Tuberculosis,2011

4. Antimicrobial resistance in acinetobacter baumannii: from bench to bedside;Lin;World J. Clin. Cases WJCC,2014

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