Amide Derivatives of [5-Chloro-6-(2-chloro/fluorobenzoyl)-2-benzoxazolinone-3-yl]acetic Acids as Potential Analgesic and Anti-Inflammatory Compounds

In this study, we have explored the prevention of gastric side effects such as gastric lesions and bleeding while maintaining the high analgesic and anti‐inflammatory activities by the derivatization of the carboxylate moiety into amides in [5‐chloro‐6‐(2‐chloro/fluorobenzoyl)‐2‐benzoxazolinone‐3‐yl...

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Veröffentlicht in:Archiv der Pharmazie (Weinheim) 2003-07, Vol.336 (4-5), p.251-257
Hauptverfasser: Banoglu, Erden, Okçelik, Berna, Kupeli, Esra, Ünlü, Serdar, Yeşilada, Erdem, Amat, Merc?, Caturla, Joan F., Sahin, M. Fethi
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Sprache:eng
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Zusammenfassung:In this study, we have explored the prevention of gastric side effects such as gastric lesions and bleeding while maintaining the high analgesic and anti‐inflammatory activities by the derivatization of the carboxylate moiety into amides in [5‐chloro‐6‐(2‐chloro/fluorobenzoyl)‐2‐benzoxazolinone‐3‐yl]acetic acids. We have tested the analgesic and anti‐inflammatory activities of the synthesized compounds in vivo by using p‐benzoquinone‐induced writhing test and carrageenan‐induced hind paw edema model, respectively. Compounds 3a, 3d, 3e, 3j and 3k potent analgesic and anti‐inflammatory activities without gastric lesions in the tested animals. Therefore, conversion of the carboxylate moiety into certain amide derivatives generated potent analgesic and anti‐inflammatory compounds while eliminating the gastrointestinal side effects. Cyclooxygenase (COX)‐selectivity of the active compounds was also investigated by using in vitro human whole blood assay. Compounds 3a, 3e, 3h and 3k selective inhibition of COX‐2 to some extent although the inhibitory activity was not very potent.
ISSN:0365-6233
1521-4184
DOI:10.1002/ardp.200300723