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article · RSC Advances

Design and synthesis of novel 2-(2-(4-bromophenyl)quinolin-4-yl)-1,3,4-oxadiazole derivatives as anticancer and antimicrobial candidates: <i>in vitro</i> and <i>in silico</i> studies

Abstract

. Compounds 17b, 17d and 17e displayed the most potent inhibitory activity, exhibiting 4-, 16- and 8-fold more activity, respectively, than the reference neomycin. Hence, we can conclude that the afforded compounds can be used as lead dual anticancer and antimicrobial candidates for future optimization.

Research topics

  • Synthesis and biological activity
  • Click Chemistry and Applications
  • Synthesis and Biological Evaluation

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DOI: 10.1039/d4ra06712f

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