Design and synthesis of oxadiazolidinediones as inhibitors of plasminogen activator inhibitor-1
摘要:
A novel series of PAI-1 inhibitors containing an oxadiazolidinedione moiety were identified by high through-put screening. Optimization of substituents by parallel synthesis and the iterative design toward understanding structure-activity relationship to improve potency are described. (C) 2004 Elsevier Ltd. All rights reserved.
Regioselectivity in the Syntheses of Enantiopure 2-Benzopyrans through Intramolecular Cyclization of Tethered Lactaldehydes. Conformations of the Products
The invention provides compounds of Formula (I):
as described herein, along with pharmaceutically acceptable salts, pharmaceutical compositions containing such compounds, and methods to use these compounds, salts and compositions for treating viral infections.
[EN] ANTIVIRAL 1,3-DI-OXO-INDENE COMPOUNDS<br/>[FR] COMPOSÉS DE 1,3-DI-OXO-INDÈNE ANTIVIRAUX
申请人:NOVARTIS AG
公开号:WO2021214080A1
公开(公告)日:2021-10-28
The invention provides compounds of Formula (I): as described herein, along with pharmaceutically acceptable salts, pharmaceutical compositions containing such compounds, and methods to use these compounds, salts and compositions for treating viral infections.