Lysine sulfonamides as novel HIV-protease inhibitors: Nε-Acyl aromatic α-amino acids
作者:Brent R. Stranix、Jean-François Lavallée、Guy Sévigny、Jocelyn Yelle、Valérie Perron、Nicholas LeBerre、Dominik Herbart、Jinzi J. Wu
DOI:10.1016/j.bmcl.2006.04.011
日期:2006.7
A series of lysine sulfonamide analogues bearing N epsilon-acyl aromatic amino acids were synthesized using an efficient synthetic route. Evaluation of these novel protease inhibitors revealed compounds with high potency against wild-type and multiple-protease inhibitor-resistant HIV viruses. (c) 2006 Elsevier Ltd. All rights reserved.
SMALL MOLECULE ACTIVATORS OF TIE-2
申请人:Aerpio Pharmaceuticals, Inc.
公开号:US20210147404A1
公开(公告)日:2021-05-20
Disclosed herein are compounds effective for activation of Tie-2 and inhibition of HPTP-beta. The compounds can provide effective therapy for vascular disorders that can include, for example, retinopathies, ocular edema, and ocular neovascularization.