Synthesis and pharmacological evaluation of new flosulide analogues, synthesized from natural safrole

AS Lages, KCM Silva, ALP Miranda, CAM Fraga…

Index: Lages, Adriana S.; Silva, Kelli C. M.; Miranda, Ana L. P.; Fraga, Carlos A. M.; Barreiro, Eliezer J. Bioorganic and Medicinal Chemistry Letters, 1998 , vol. 8, # 2 p. 183 - 188

Full Text: HTML

Citation Number: 28

Abstract

Four new aryl-sulfonamide derivatives (3a, 4a, 5a∼ b), having methylenedioxy group attached to phenyl ring, were prepared from natural safrole and evaluated as anti- inflammatory agents. The N-methylsulfonamide 3a and corresponding retrosulfonamide derivative 5a were more active than standards indomethacin and nimesulide, at the same molar concentration, in carrageenan-induced pleurisy assay.

Related Articles:

Nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: stereospecific formation of diarylalkanes and triarylmethanes

[Maity, Prantik; Shacklady-Mcatee, Danielle M.; Yap, Glenn P. A.; Sirianni, Eric R.; Watson, Mary P. Journal of the American Chemical Society, 2013 , vol. 135, # 1 p. 280 - 285]

Nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: stereospecific formation of diarylalkanes and triarylmethanes

[Maity, Prantik; Shacklady-Mcatee, Danielle M.; Yap, Glenn P. A.; Sirianni, Eric R.; Watson, Mary P. Journal of the American Chemical Society, 2013 , vol. 135, # 1 p. 280 - 285]

More Articles...