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Structure-activity relationship studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a potent inhibitor of leukotriene A(4) (LTA(4)) hydrolase.
Penning, T D; Chandrakumar, N S; Chen, B B; Chen, H Y; Desai, B N; Djuric, S W; Docter, S H; Gasiecki, A F; Haack, R A; Miyashiro, J M; Russell, M A; Yu, S S; Corley, D G; Durley, R C; Kilpatrick, B F; Parnas, B L; Askonas, L J; Gierse, J K; Harding, E I; Highkin, M K; Kachur, J F; Kim, S H; Krivi, G G; Villani-Price, D; Pyla, E Y; Smith, W G.
Afiliação
  • Penning TD; Departments of Medicinal Chemistry, Structure-Activity Screening Program, Inflammatory Diseases Research, and Molecular Pharmacology, Searle Research and Development, Monsanto Company, Skokie, Illinois 60077, USA. thomas.d.penning@monsanto.com
J Med Chem ; 43(4): 721-35, 2000 Feb 24.
Article em En | MEDLINE | ID: mdl-10691697
Leukotriene B(4) (LTB(4)) is a pro-inflammatory mediator that has been implicated in the pathogenesis of a number of diseases including inflammatory bowel disease (IBD) and psoriasis. Since the action of LTA(4) hydrolase is the rate-limiting step for LTB(4) production, this enzyme represents an attractive pharmacological target for the suppression of LTB(4) production. From an in-house screening program, SC-22716 (1, 1-[2-(4-phenylphenoxy)ethyl]pyrrolidine) was identified as a potent inhibitor of LTA(4) hydrolase. Structure-activity relationship (SAR) studies around this structural class resulted in the identification of a number of novel, potent inhibitors of LTA(4) hydrolase, several of which demonstrated good oral activity in a mouse ex vivo whole blood assay.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirrolidinas / Inibidores Enzimáticos / Epóxido Hidrolases Limite: Animals / Humans / Male Idioma: En Revista: J Med Chem Assunto da revista: QUIMICA Ano de publicação: 2000 Tipo de documento: Article País de afiliação: Estados Unidos
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirrolidinas / Inibidores Enzimáticos / Epóxido Hidrolases Limite: Animals / Humans / Male Idioma: En Revista: J Med Chem Assunto da revista: QUIMICA Ano de publicação: 2000 Tipo de documento: Article País de afiliação: Estados Unidos