Design and synthesis of selective keto-1,2,4-oxadiazole-based tryptase inhibitors
摘要:
Using a scaleable, directed library approach based on orthogonally protected advanced intermediates, we have prepared a series of potent keto-1,2,4-oxadiazoles designed to explore the P-2 binding pocket of human mast cell tryptase, while building in a high degree of selectivity over human trypsin and other serine proteases. (c) 2006 Elsevier Ltd. All rights reserved.
[EN] ACTIVE KETONE INHIBITORS OF TRYPTASE<br/>[FR] INHIBITEURS DE LA TRYPTASE, CONTENANT DE LA CETONE ACTIVE
申请人:AXYS PHARM INC
公开号:WO2006044133A1
公开(公告)日:2006-04-27
[EN] The present invention related to certain active tetracyclic ketone inhibitors of tryptase, pharmaceutical composition comprising these compounds and methods of treating asthma, allergic rhinitis, and/or Chronic Obstructive Pulmonary Disease utilizing these compounds. [FR] La présente invention concerne certains inhibiteurs de la tryptase, contenant de la cétone active, une composition pharmaceutique renfermant ces composés et des méthodes de traitement de l'asthme, de la rhinite allergique et/ou d'une maladie pulmonaire obstructive chronique, au moyen de ces composés.