Discovery of 2-Methyl-5-(1H-pyrazol-4-yl)pyridines and Related Heterocycles as Promising M4 mAChR Positive Allosteric Modulators for the Treatment of Neurocognitive Disorders.

IF 6.8 1区 医学 Q1 CHEMISTRY, MEDICINAL
Journal of Medicinal Chemistry Pub Date : 2024-08-08 Epub Date: 2024-07-18 DOI:10.1021/acs.jmedchem.4c01207
Boqun Liu, Geoff Thompson, Manuela Jörg, Nicholas Barnes, David M Thal, Arthur Christopoulos, Ben Capuano, Celine Valant, Peter J Scammells
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引用次数: 0

Abstract

The M4 muscarinic acetylcholine receptor (mAChR) is a biological target for neurocognitive disorders. Compound 1 is an ago-PAM for the M4 mAChR. Herein, we report the design, synthesis, and evaluation of novel putative M4 mAChR PAMs based on 1. These analogs were screened and then fully characterized in two functional assays (GoB protein activation and CAMYEL activation) to quantify their allosteric and ago-PAM properties against ACh. A selection of 7 M4 PAMs were assessed for their ability to modulate ACh-mediated β-arrestin recruitment and revealed 4 distinct clusters of M4 PAM activity: (1) analogs similar to 1 (24d), (2) analogs demonstrating only allosteric agonism (23d), (3) analogs with increased allosteric properties in CAMYEL activation (23b/23f and 24a/24b), and (4) analogs with a biased modulatory effect toward β-arrestin recruitment (23i). These novel M4 chemical tools disclose discrete molecular determinants, allowing further interrogation of the therapeutic roles of cAMP and β-arrestin pathways in neurocognitive disorders.

Abstract Image

发现 2-甲基-5-(1H-吡唑-4-基)吡啶及相关杂环作为治疗神经认知障碍的 M4 mAChR 阳性异构调节剂。
M4 肌肽乙酰胆碱受体(mAChR)是神经认知障碍的一个生物学靶点。化合物 1 是 M4 mAChR 的前 PAM。在此,我们报告了基于 1 的新型推定 M4 mAChR PAM 的设计、合成和评估。我们对这些类似物进行了筛选,然后在两种功能测试(GoB 蛋白激活和 CAMYEL 激活)中对其进行了全面表征,以量化它们对 ACh 的异构和前-PAM 特性。对筛选出的 7 种 M4 PAM 调节 ACh 介导的 β-restin 招募的能力进行了评估,发现了 4 个不同的 M4 PAM 活性集群:(1) 类似于 1 的类似物(24d),(2) 仅表现出异位激动作用的类似物(23d),(3) 在 CAMYEL 激活过程中具有更强异位特性的类似物(23b/23f 和 24a/24b),以及 (4) 对 β-restin 募集具有偏向调节作用的类似物(23i)。这些新型 M4 化学工具揭示了离散的分子决定因素,从而可以进一步研究 cAMP 和 β-restin 通路在神经认知障碍中的治疗作用。
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来源期刊
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry 医学-医药化学
CiteScore
4.00
自引率
11.00%
发文量
804
审稿时长
1.9 months
期刊介绍: The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents. The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.
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