Discovery of the First Highly M5-Preferring Muscarinic Acetylcholine Receptor Ligand, an M5 Positive Allosteric Modulator Derived from a Series of 5-Trifluoromethoxy N-Benzyl Isatins

被引:84
作者
Bridges, Thomas M.
Marlo, Joy E.
Niswender, Colleen M.
Jones, Carrie K.
Jadhav, Satyawan B.
Gentry, Patrick R.
Plumley, Hyekyung C.
Weaver, C. David
Conn, P. Jeffrey
Lindsley, Craig W. [1 ]
机构
[1] Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA
关键词
KNOCKOUT MICE; POTENTIATORS; GENES;
D O I
10.1021/jm900286j
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
This report describes the discovery and initial characterization of the first positive allosteric modulator of muscarinic acetylcholine receptor subtype 5 (mAChR5 or M5). Functional HTS, identified VU0119498, which displayed micromolar potencies for potentiation of acetylcholine at M1, M3, and M5 receptors in cell-based Ca2+ mobilization assays. Subsequent optimization led to the discovery of VU0238429, which possessed an EC50 of approximately 1.16 mu M at M5 with >30-fold selectivity versus M1 and M3, with no M2 or M4 potentiator activity.
引用
收藏
页码:3445 / 3448
页数:4
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