| Literature DB >> 2970548 |
L G Humber1, E Ferdinandi, C A Demerson, S Ahmed, U Shah, D Mobilio, J Sabatucci, B De Lange, F Labbadia, P Hughes.
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.Entities:
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Year: 1988 PMID: 2970548 DOI: 10.1021/jm00117a009
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446