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Synthesis and evaluation of curcumin analogues as cytotoxic agents
Authors:Ahmed A Fadda  Farid A Badria  Khaled M El-Attar
Institution:(1) Chemistry Department, Faculty of Science, Mansoura University, Mansoura, 35516, Egypt;(2) Pharmacognosy Department, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt
Abstract:Seventeen curcumin analogues were prepared and evaluated for in vitro and in vivo cytotoxicity against an Ehrlich ascites carcinoma (EAC). In vitro results revealed that compounds 10, 7, and 12 were the most potent analogues against EAC respectively. However, in vivo evaluation of compound 10 proved its capability to normalize the blood picture compared with 5-fluorouracil, a well-known anticancer drug.
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