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Etodolac, a novel antiinflammatory agent. The syntheses and biological evaluation of its metabolites
Journal of Medicinal Chemistry1988Vol. 31(9), pp. 1712–1719
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Leslie G. Humber, Eckhardt S. Ferdinandi, Christopher A. Demerson, Syed Waseemuddin Ahmed, Uresh Shah, Dominick Mobilio, Joseph P. Sabatucci, Barbara De Lange, Francesco Labbadia
Abstract
The syntheses of five metabolites of the antiinflammatory drug etodolac (1,8-diethyl-1,3,4,9-tetrahydropyrano-[3,4-b]indole-1-acetic acid) are described, viz. 6-hydroxyetodolac, N-methyletodolac, 4-ureidoetodolac, 8-(1'-hydroxy)etodolac, and 4-oxoetodolac. These syntheses were used to confirm the identities of the metabolites. The metabolites themselves, as well as the previously reported metabolite 7-hydroxyetodolac, were tested in a rat adjuvant edema model and in vitro for their capacity to block prostaglandin production in chondrocyte cells. All either were inactive or possessed only marginal activity. The isolation of N-methyletodolac and 4-oxoetodolac from human and rat urine, respectively, is also described.
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