Iminosugar-ferrocene conjugates as potential anticancer agents.

作者: Audrey Hottin , Faustine Dubar , Agata Steenackers , Philippe Delannoy , Christophe Biot

DOI: 10.1039/C2OB25727K

关键词:

摘要: We prepared a series of new iminosugar–ferrocene hybrids displaying potent inhibition fucosidase (bovine kidney) and inactivation MDA-MB-231 breast cancer cells proliferation at low micromolar concentrations. The synthetic route brought to light an unprecedented isomerisation 2-ethanalylpyrrolidine.

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