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Abstract #122948 Published in IGR 25-1

Iodine/Oxone® oxidative system for the synthesis of selenylindoles bearing a benzenesulfonamide moiety as carbonic anhydrase I, II, IX, and XII inhibitors

Palomba M; Angeli A; Galdini R; Hughineata AJ; Perin G; Lenardão EJ; Marini F; Santi C; Supuran CT; Bagnoli L
Organic & biomolecular chemistry 2024; 22: 6532-6542


A wide range of 3-selenylindoles were synthesized an eco-friendly approach that uses Oxone® as the oxidant in the presence of a catalytic amount of iodine. This mild and economical protocol showed broad functional group tolerance and operational simplicity. A series of novel selenylindoles bearing a benzenesulfonamide moiety were also synthesized and evaluated as carbonic anhydrase inhibitors of the human (h) isoforms hCa I, II, IX, and XII, which are involved in pathologies such as glaucoma and cancer. Several derivatives showed excellent inhibitory activity towards these isoforms in the nanomolar range, lower than that shown by acetazolamide.

Department of Pharmaceutical Sciences (Group of Catalysis, Synthesis and Organic Green Chemistry), University of Perugia, Via del Liceo, 1-06123 Perugia, Italy. luana.bagnoli@unipg.it.

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15 Miscellaneous



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