An efficient synthesis and biological screening of benzofuran and benzo[ d ]isothiazole derivatives for Mycobacterium tuberculosis DNA GyrB inhibition-Reference-Cited by-同舟云学术

An efficient synthesis and biological screening of benzofuran and benzo[ d ]isothiazole derivatives for Mycobacterium tuberculosis DNA GyrB inhibition

Published:2014-12 Issue:23 Volume:22 Page:6552-6563
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Reddy Kummetha Indrasena,Srihari Konduri,Renuka Janupally,Sree Komanduri Shruthi,Chuppala Aruna,Jeankumar Variam Ullas,Sridevi Jonnalagadda Padma,Babu Kondra Sudhakar,Yogeeswari Perumal,Sriram Dharmarajan

Publisher

Elsevier BV

Subject

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

Reference24 articles.

1. Thiazolopyridine Ureas as Novel Antitubercular Agents Acting through Inhibition of DNA Gyrase B

2. Schiff Bases of Indoline-2,3-dione: Potential Novel Inhibitors of Mycobacterium Tuberculosis (Mtb) DNA Gyrase

3. World Health Organization. Global Tuberculosis Control; WHO 2011 Report on Tuberculosis. http://www.who.int/mediacentre/news/releases/2011/tb_20111011/en/index.html.

4. World Health Organization. Multidrug and Extensively Drug-Resistant TB (M/XDR-TB); WHO 2010 Global Report on Surveillance and Response.

5. Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence

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