Article ID Journal Published Year Pages File Type
7801483 European Journal of Medicinal Chemistry 2013 12 Pages PDF
Abstract
Design and diversity oriented synthesis of bis heterocycles with quinoline moiety as central key heterocycle and parallel library generation achieved. Promising antitubercular activity obtained along with SAR and low cytotoxicity.
Keywords
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
Design, diversity-oriented synthesis and structure activity relationship studies of quinolinyl heterocycles as antimycobacterial agents
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