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Substituted 2-pyridinemethanol derivatives as potent and selective phosphodiesterase-4 inhibitors.
Ducharme, Yves; Friesen, Richard W; Blouin, Marc; Côté, Bernard; Dubé, Daniel; Ethier, Diane; Frenette, Richard; Laliberté, France; Mancini, Joseph A; Masson, Paul; Styhler, Angela; Young, Robert N; Girard, Yves.
Afiliación
  • Ducharme Y; Merck Frosst Centre for Therapeutic Research, PO Box 1005, Pointe Claire-Dorval, Québec, Canada H9R 4P8. yves_ducharme@merck.com
Bioorg Med Chem Lett ; 13(11): 1923-6, 2003 Jun 02.
Article en En | MEDLINE | ID: mdl-12749899
The synthesis and the phosphodiesterase-4 (PDE4) inhibitory activity of 2-pyridinemethanol derivatives is described. The evaluation of the structure-activity relationship (SAR) in this series of novel PDE4 inhibitors led to the identification of compound 9 which exhibits excellent in vitro activity, desirable pharmacokinetic parameters and good efficacy in animal models of bronchoconstriction.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inhibidores de Fosfodiesterasa / Picolinas / 3',5'-AMP Cíclico Fosfodiesterasas Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Bioorg Med Chem Lett Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2003 Tipo del documento: Article
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inhibidores de Fosfodiesterasa / Picolinas / 3',5'-AMP Cíclico Fosfodiesterasas Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Bioorg Med Chem Lett Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2003 Tipo del documento: Article
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