Sansanmycin natural product analogues as potent and selective anti-mycobacterials that inhibit lipid I biosynthesis-Reference-Cited by-同舟云学术

Sansanmycin natural product analogues as potent and selective anti-mycobacterials that inhibit lipid I biosynthesis

Published:2017-03-01 Issue:1 Volume:8 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Tran Anh T.,Watson Emma E.,Pujari Venugopal,Conroy Trent,Dowman Luke J.,Giltrap Andrew M.,Pang Angel,Wong Weng Ruh,Linington Roger G.^ORCID,Mahapatra Sebabrata,Saunders Jessica,Charman Susan A.,West Nicholas P.,Bugg Timothy D. H.,Tod Julie,Dowson Christopher G.,Roper David I.^ORCID,Crick Dean C.,Britton Warwick J.,Payne Richard J.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms14414.pdf

Reference43 articles.

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3. Gandhi, N. R. et al. Extensively drug-resistant tuberculosis as a cause of death in patients co-infected with tuberculosis and HIV in a rural area of South Africa. Lancet 368, 1575–1580 (2006).

4. Chahine, E. B., Karaoui, L. R. & Mansour, H. Bedaquiline: a novel diarylquinoline for multidrug-resistant tuberculosis. Ann. Pharmacother. 48, 107–115 (2014).

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