Literature DB >> 2970548

Etodolac, a novel antiinflammatory agent. The syntheses and biological evaluation of its metabolites.

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.

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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


  3 in total

1.  Copper-Catalyzed Enantioselective Hydroalkoxylation of Alkenols for the Synthesis of Cyclic Ethers.

Authors:  Dake Chen; Ilyas A Berhane; Sherry R Chemler
Journal:  Org Lett       Date:  2020-06-04       Impact factor: 6.005

Review 2.  Etodolac clinical pharmacokinetics.

Authors:  D R Brocks; F Jamali
Journal:  Clin Pharmacokinet       Date:  1994-04       Impact factor: 6.447

Review 3.  Continuous Flow Synthesis of Heterocycles: A Recent Update on the Flow Synthesis of Indoles.

Authors:  Marco Colella; Leonardo Degennaro; Renzo Luisi
Journal:  Molecules       Date:  2020-07-16       Impact factor: 4.411

  3 in total

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