Gamma Secretase Modulators: New Alzheimer's Drugs on the Horizon?

被引:108
作者
Bursavich, Matthew G. [1 ]
Harrison, Bryce A. [1 ]
Blain, Jean-Francois [1 ]
机构
[1] FORUM Pharmaceut, 225 Second Ave, Waltham, MA 02451 USA
关键词
AMYLOID PRECURSOR PROTEIN; A-BETA PEPTIDES; TRANSMEMBRANE DOMAIN; IN-VITRO; BICYCLIC HETEROCYCLES; MISSENSE MUTATIONS; DISEASE; DISCOVERY; POTENT; DESIGN;
D O I
10.1021/acs.jmedchem.5b01960
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The rapidly aging population desperately requires new therapies for Alzheimer's disease. Despite years of pharmaceutical research, limited clinical success has been realized, with several failed disease modification therapies in recent years. On the basis of compelling genetic evidence, the pharmaceutical industry has put a large emphasis on brain-beta amyloid (A beta) either through its removal via antibodies or by targeting the proteases responsible for its production. In this Perspective, we focus on the development of small molecules that improve the activity of one such protease, gamma secretase, through an allosteric binding site to preferentially increase the concentration of the shorter not,amyloidogenic A beta species. After a few early failures due to poor drug-like properties, the industry is now on the cusp of delivering gamma secretase modulators for clinical proof-of-mechanism studies that combine potency and efficacy with improved drug-like properties such as. lower cLogP, high central nervous system multiparameter optimization scores, and high spa character.
引用
收藏
页码:7389 / 7409
页数:21
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