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Synthesis and cytotoxic studies of a new series of pyridinoxymethylcoumarins

Abstract

A series of 3-​(pyridin-​3-​yloxymethyl)​-​chromen-​2-​ones were synthesized by the reaction of substituted 4-​bromomethylcoumarins with 3-​hydroxypyridines. The synthesized compds. were screened for their cytotoxic activities against Dalton's ascitic lymphoma (DAL) and Ehrlich ascites carcinoma (EAC) cell lines. The 2-​(2-​Methyl-​pyridin-​3-​yloxymethyl)​-​benzo[f]​chromen-​3-​one was found to be the most cytotoxic against DAL cell line and 6-​Isopropyl-​3-​(2-​methyl-​pyridin-​3-​yloxymethyl)​-​chromen-​2-​one was found to be the most cytotoxic against EAC cell line

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