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A new class of leukotriene biosynthesis inhibitor: the development of MK-0591.
Prasit, P; Belley, M; Blouin, M; Brideau, C; Chan, C; Charleson, S; Evans, J F; Frenette, R; Gauthier, J Y; Guay, J.
Afiliação
  • Prasit P; Merck Frosst Centre for Therapeutic Research, Pointe Claire-Dorval, Québec, Canada.
J Lipid Mediat ; 6(1-3): 239-44, 1993.
Article em En | MEDLINE | ID: mdl-8357985
ABSTRACT
The evolution of MK-0591 (3-[1-(4-chlorobenzyl)-3-(t-butylthio)-5-(quinolin-2-ylmethoxy+ ++)indol-2-yl]- 2,2-dimethylpropanoic acid), 12, a potent, orally active leukotriene biosynthesis inhibitor is described. MK-0591 is currently undergoing clinical evaluation as a potential agent for the treatment of asthma and inflammatory bowel disease. It acts through a novel mechanism by a specific interaction with a membrane protein, 5-lipoxygenase activating protein (FLAP), which has been shown to be essential for LT synthesis in inflammatory cells. A brief comparison of its biological activity with that of its progenitors MK-886 and L-674,636 is described.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinolinas / Leucotrienos / Antagonistas de Leucotrienos / Indóis Limite: Humans Idioma: En Revista: J Lipid Mediat Ano de publicação: 1993 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinolinas / Leucotrienos / Antagonistas de Leucotrienos / Indóis Limite: Humans Idioma: En Revista: J Lipid Mediat Ano de publicação: 1993 Tipo de documento: Article