Identification of heteroarylenamines as a new class of antituberculosis lead molecules

Bioorganic and Medicinal Chemistry Letters

Volumn 15, Issue 18, 2005, Pages 4097-4099

  Copp, Brent R ^a   Christiansen, Holly C ^a   Lindsay, Brent S ^a   G Franzblau, Scott ^b  

^a UNIVERSITY OF AUCKLAND   (New Zealand)

^b UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

Author keywords

Antituberculosis activity; Enamine; Quinone; Tuberculosis

Indexed keywords

ACRIDINE; ASCIDIDEMIN; CIPROFLOXACIN; ENAMINE; ETHAMBUTOL; ISONIAZID; KANAMYCIN; LEAD; QUINONE DERIVATIVE; RIFAMPICIN; TUBERCULOSTATIC AGENT;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BACTERIAL STRAIN; CONTROLLED STUDY; DRUG IDENTIFICATION; DRUG MECHANISM; DRUG SCREENING; DRUG SELECTIVITY; DRUG SYNTHESIS; MINIMUM INHIBITORY CONCENTRATION; MONKEY; MOUSE; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; OBSERVATION;

AMINES; ANTITUBERCULAR AGENTS; DRUG EVALUATION, PRECLINICAL; DRUG RESISTANCE; INHIBITORY CONCENTRATION 50; MOLECULAR STRUCTURE; MYCOBACTERIUM TUBERCULOSIS; STRUCTURE-ACTIVITY RELATIONSHIP;

MYCOBACTERIUM TUBERCULOSIS H37RV;

EID: 23644446623     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2005.06.010     Document Type: Article

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