We report herein the synthesis, biological evaluation and docking analysis of a new series of methylsulfonyl, sulfamoyl acetamides and ethyl acetates that selectively inhibit cyclooxygenase-2 (COX-2) isoform. Among the newly synthesized compounds, some of them were endowed with a good activity against COX-2 and a good selectivity COX-2/COX-1 in vitro as well as a desirable analgesic activity in vivo, proving that replacement of the ester moiety with an amide group gave access to more stable derivatives, characterized by a good COX-inhibition.

Consalvi, S., Alfonso, S., DI CAPUA, A., Poce, G., Pirolli, A., Sabatino, M., et al. (2015). Synthesis, biological evaluation and docking analysis of a new series of methylsulfonyl and sulfamoyl acetamides and ethyl acetates as potent COX-2 inhibitors. BIOORGANIC & MEDICINAL CHEMISTRY, 23(4), 810-820 [10.1016/j.bmc.2014.12.041].

Synthesis, biological evaluation and docking analysis of a new series of methylsulfonyl and sulfamoyl acetamides and ethyl acetates as potent COX-2 inhibitors

DI CAPUA, ANGELA;ANZINI, MAURIZIO;
2015-01-01

Abstract

We report herein the synthesis, biological evaluation and docking analysis of a new series of methylsulfonyl, sulfamoyl acetamides and ethyl acetates that selectively inhibit cyclooxygenase-2 (COX-2) isoform. Among the newly synthesized compounds, some of them were endowed with a good activity against COX-2 and a good selectivity COX-2/COX-1 in vitro as well as a desirable analgesic activity in vivo, proving that replacement of the ester moiety with an amide group gave access to more stable derivatives, characterized by a good COX-inhibition.
2015
Consalvi, S., Alfonso, S., DI CAPUA, A., Poce, G., Pirolli, A., Sabatino, M., et al. (2015). Synthesis, biological evaluation and docking analysis of a new series of methylsulfonyl and sulfamoyl acetamides and ethyl acetates as potent COX-2 inhibitors. BIOORGANIC & MEDICINAL CHEMISTRY, 23(4), 810-820 [10.1016/j.bmc.2014.12.041].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/975003