Preliminary Structure–Activity Relationships and Biological Evaluation of Novel Antitubercular Indolecarboxamide Derivatives Against Drug-Susceptible and Drug-Resistant Mycobacterium tuberculosis Strains

Author:

Onajole Oluseye K.1,Pieroni Marco1,Tipparaju Suresh K.1,Lun Shichun2,Stec Jozef1,Chen Gang1,Gunosewoyo Hendra1,Guo Haidan2,Ammerman Nicole C.23,Bishai William R.234,Kozikowski Alan P.1

Affiliation:

1. Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, 833 South Wood Street, Chicago, Illinois 60612, United States

2. Center for Tuberculosis Research, Department of Medicine, Division of Infectious Disease, Johns Hopkins School of Medicine, Baltimore, Maryland 21231-1044, United States

3. KwaZulu-Natal Research Institute for Tuberculosis and HIV, Nelson R. Mandela School of Medicine, 719 Umbilo Road, Durban 4001, KwaZulu-Natal, South Africa

4. Howard Hughes Medical Institute, 4000 Jones Bridge Road, Chevy Chase, Maryland 20815-6789, United States

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Reference32 articles.

1. Tuberculosis;Fact Sheet no. 104;World Health Organisation:Geneva, 2013; http://www.who.int/mediacentre/factsheets/fs104/en/index.html(accessed February 11, 2013).

2. Global Tuberculosis Report 2012;World Health Organisation:Geneva, 2012; http://apps.who.int/iris/bitstream/10665/75938/1/9789241564502_eng.pdf(accessed January 8, 2013).

3. Directly observed therapy (DOT) for tuberculosis: why, when, how and if?

4. Epidemiology and Challenges to the Elimination of Global Tuberculosis

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