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Published on: May 9, 2025
Linker-modified quinoline derivatives targeting HIV-1 integrase: synthesis and biological activity
Christophe Bénard1, Fatima Zouhiri, Marie Normand-Bayle
1CNRS UMR 8076, Centre d'Etudes Pharmaceutiques, Chimie Organique, 5 rue J.-B. Clément, 92296 Châtenay-Malabry, France.
Abstract:
A novel series of HIV-1 integrase inhibitors was synthesized and tested in both in vitro and ex vivo assays. These inhibitors are featured by the presence of a quinoline subunit and an ancillary aromatic ring linked by functionalized spacers such as amide, hydrazide, urea and 1-hydroxyprop-1-en-3-one moiety. Amide derivatives are the most promising ones and could serve as leads for further developments.
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