Discovery of a novel [3.2.1] benzo fused bicyclic sulfonamide-pyrazoles as potent, selective and efficacious γ-secretase inhibitors

被引:10
|
作者
Ye, Xiaocong M. [1 ]
Konradi, Andrei W. [1 ]
Sun, Minghua [1 ]
Yuan, Shendong [1 ]
Aubele, Danielle L. [1 ]
Dappen, Michael [1 ]
Dressen, Darren [1 ]
Garofalo, Albert W. [1 ]
Jagodzinski, Jacek J. [1 ]
Latimer, Lee [1 ]
Probst, Gary D. [1 ]
Sham, Hing L. [1 ]
Wone, David [1 ]
Xu, Ying-zi [1 ]
Ness, Daniel [2 ]
Brigham, Elizabeth [2 ]
Kwong, Grace T. [2 ]
Willtis, Chris [2 ]
Tonn, George [3 ]
Goldbach, Erich [3 ]
Quinn, Kevin P. [3 ]
Zhang, Hongbin H. [3 ]
Sauer, John-Michael [3 ]
Bova, Michael [4 ]
Basi, Guriqbal S. [5 ]
机构
[1] Elan Pharmaceut, Dept Med Chem, San Francisco, CA 94080 USA
[2] Elan Pharmaceut, Dept Pharmacol, San Francisco, CA 94080 USA
[3] Elan Pharmaceut, Dept Drug Metab & Pharmacokinet, San Francisco, CA 94080 USA
[4] Elan Pharmaceut, Dept Assay Dev, San Francisco, CA 94080 USA
[5] Elan Pharmaceut, Dept Biol, San Francisco, CA 94080 USA
关键词
Alzheimer's disease; Amyloid precursor protein; gamma-Secretase; gamma-Secretase inhibitor; Notch; ALZHEIMERS-DISEASE; GENES;
D O I
10.1016/j.bmcl.2012.12.039
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Structure-activity relationship (SAR) of a novel, potent and metabolically stable series of benzo [3.2.1] bicyclic sulfonamide-pyrazoles as gamma-secretase inhibitors are described. Compounds that are efficacious in reducing the cortical A beta x-40 levels in FVB mice via oral dose, as well as those with high selectivity over Notch, are highlighted. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:996 / 1000
页数:5
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