Facile Synthesis of Chiral Phenylselenides As Novel Antioxidants and Cytotoxic Agents
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Organoselenium compounds are well-known for their unique biological properties, including antioxidant, anticancer and anti-inflammatory. They result from the presence of a particular Se-moiety enclosed in a structure that provides physicochemical features necessary for effective drug-target interactions. Looking for a proper drug design that considers the influence of each structural element has to be conducted. In this paper, we have synthesized a series of chiral phenylselenides, possessing an additional -substituted amide moiety, and evaluated their antioxidant and anticancer potential. The presented derivatives, as a group of enantiomeric and diastereomeric pairs, enabled a thorough investigation of the 3D structure-activity dependence in correlation with the presence of the phenylselanyl group as the potential pharmacophore. The -indanyl derivatives possessing a - and -2-hydroxy group were selected as the most promising antioxidants and anticancer agents.
Laskowska A, Pacula-Miszewska A, Obieziurska-Fabisiak M, Jastrzebska A, Dlugosz-Pokorska A, Gach-Janczak K Molecules. 2024; 29(12).
PMID: 38930931 PMC: 11206731. DOI: 10.3390/molecules29122866.
Laskowska A, Pacula-Miszewska A, Obieziurska-Fabisiak M, Jastrzebska A, Dlugosz-Pokorska A, Gach-Janczak K Materials (Basel). 2024; 17(4).
PMID: 38399148 PMC: 10890689. DOI: 10.3390/ma17040899.