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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.
论文数: 0 引用数: 0
h-index: 0
机构: Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA

Marlo, Joy E.
论文数: 0 引用数: 0
h-index: 0
机构: Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA

Niswender, Colleen M.
论文数: 0 引用数: 0
h-index: 0
机构: Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA

Jones, Carrie K.
论文数: 0 引用数: 0
h-index: 0
机构: Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA

Jadhav, Satyawan B.
论文数: 0 引用数: 0
h-index: 0
机构: Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA

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Plumley, Hyekyung C.
论文数: 0 引用数: 0
h-index: 0
机构: Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA

Weaver, C. David
论文数: 0 引用数: 0
h-index: 0
机构: Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA

Conn, P. Jeffrey
论文数: 0 引用数: 0
h-index: 0
机构: Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA

Lindsley, Craig W.
论文数: 0 引用数: 0
h-index: 0
机构:
Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA Vanderbilt Univ, Vanderbilt Program Drug Discovery, Dept Pharmacol, Med Ctr, Nashville, TN 37232 USA
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.
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页码:3445 / 3448
页数:4
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机构:
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Kim, Kwangho
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Orton, Darren
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机构:
Vanderbilt Univ, Dept Chem, Nashville, TN 37232 USA
Vanderbilt Univ, Inst Biol Chem, Nashville, TN 37232 USA Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA

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Vanderbilt Univ, Inst Biol Chem, Nashville, TN 37232 USA Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA

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Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
Vanderbilt Univ, Program Drug Discovery, Nashville, TN 37232 USA
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