Synthesis, Docking and Biological Evaluation of Some Novel 5-bromo-2-(5-aryl-1, 3, 4-thiadiazol-2-yl) isoindoline-1, 3-dione Derivatives Targeting ATP-binding Site of …

A Gupta, P Singh, B Kamble, A Kulkarni…

文献索引：Gupta, Ankur; Singh, Priya; Kamble, Bhagyashree; Kulkarni, Aditi; Chandrasekar, Moola Joghee Nanjan Letters in Drug Design and Discovery, 2012 , vol. 9, # 7 p. 668 - 675

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被引用次数: 8

摘要

Human Topoisomerase IIα (htopoIIα) is an approved and validated target for designing anticancer agents. Among the various methods to block the functions of htopoIIα, targeting ATP site for its competitive inhibition has been relatively less investigated. Therefore, to identify some novel htopoIIα inhibitors to target the ATP-binding site, we designed and synthesized a small library of 5-aryl-1, 3, 4-thiadiazole coupled phthalimide derivatives ...