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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >3-(Pyridin-2-yl-ethynyl)benzamide metabotropic glutamate receptor 5 negative allosteric modulators: hit to lead studies.
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3-(Pyridin-2-yl-ethynyl)benzamide metabotropic glutamate receptor 5 negative allosteric modulators: hit to lead studies.

机译:3-(吡啶-2-基-乙炔基)苯甲酰胺代谢型谷氨酸受体5个负变构调节剂:牵头研究。

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摘要

A series of 3-(pyridin-2-yl-ethynyl)benzamide negative allosteric modulators of the metabotropic glutamate receptor 5 (mGluR5 NAMs) have been prepared. Starting from HTS hit 1 (IC(50): 926 nM), potent mGluR5 NAMs showing excellent potencies (IC(50)s<50 nM) and good physicochemical profiles were prepared by monitoring LipE values. One compound 26 showed excellent mGluR5 binding (K(i): 21 nM) and antagonism (IC(50): 8 nM), an excellent rat PK profile (CL: 12 mL/min/kg, %F: 85) and showed oral activity in a mouse 4-Plate Behavioral model of anxiety (MED: 30 mpk) and a mouse Stress Induced Hyperthermia model of anxiety (MED 17.8 mpk).
机译:制备了一系列代谢型谷氨酸受体5(mGluR5 NAM)的3-(吡啶-2-基-乙炔基)苯甲酰胺负变构调节剂。从HTS 1(IC(50):926 nM)开始,通过监测LipE值制备了显示出出色效价(IC(50)s <50 nM)和良好理化特性的有效mGluR5 NAM。一种化合物26显示出出色的mGluR5结合(K(i):21 nM)和拮抗作用(IC(50):8 nM),出色的大鼠PK谱(CL:12 mL / min / kg,%F:85)小鼠4-Plate焦虑行为模型(MED:30 mpk)和小鼠应激诱导的焦虑症高热模型(MED 17.8 mpk)的口服活性。

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