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 againstCOX-2 and a good selectivity COX-2/COX-1 in vitro as well as a desirable analgesic activity in vivo, provingthat replacement of the ester moiety with an amide group gave access to more stable derivatives,characterized by a good COX-inhibition.

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

Consalvi, Sara;
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 againstCOX-2 and a good selectivity COX-2/COX-1 in vitro as well as a desirable analgesic activity in vivo, provingthat replacement of the ester moiety with an amide group gave access to more stable derivatives,characterized by a good COX-inhibition.
2015
Inglese
Inglese
23
4
810
820
11
http://www.journals.elsevier.com/bioorganic-and-medicinal-chemistry/
Esperti anonimi
Analgesic agents
Anti-inflammatory agents
COX-2 inhibitors
Diarylpyrroles
Medicinal chemistry
Internazionale
13
info:eu-repo/semantics/article
262
Consalvi, Sara; Alfonso, Salvatore; Di Capua, Angela; Poce, Giovanna; Pirolli, Adele; Sabatino, Manuela; Ragno, Rino; Anzini, Maurizio; Sartini, Stefa...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14085/22450
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