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孔中的腈基:在神经元型一氧化氮合酶中发现一个小的辅助口袋,从而开发出强效且选择性的2-氨基喹啉抑制剂。

Nitrile in the Hole: Discovery of a Small Auxiliary Pocket in Neuronal Nitric Oxide Synthase Leading to the Development of Potent and Selective 2-Aminoquinoline Inhibitors.

作者信息

Cinelli Maris A, Li Huiying, Chreifi Georges, Poulos Thomas L, Silverman Richard B

机构信息

Department of Chemistry, Department of Molecular Biosciences, Chemistry of Life Processes Institute, Center for Molecular Innovation and Drug Discovery, Northwestern University , 2145 Sheridan Road, Evanston, Illinois 60208-3113, United States.

Departments of Molecular Biology and Biochemistry, Pharmaceutical Sciences, and Chemistry, University of California, Irvine , Irvine, California 92697-3900, United States.

出版信息

J Med Chem. 2017 May 11;60(9):3958-3978. doi: 10.1021/acs.jmedchem.7b00259. Epub 2017 Apr 19.

Abstract

Neuronal nitric oxide synthase (nNOS) inhibition is a promising strategy to treat neurodegenerative disorders, but the development of nNOS inhibitors is often hindered by poor pharmacokinetics. We previously developed a class of membrane-permeable 2-aminoquinoline inhibitors and later rearranged the scaffold to decrease off-target binding. However, the resulting compounds had decreased permeability, low human nNOS activity, and low selectivity versus human eNOS. In this study, 5-substituted phenyl ether-linked aminoquinolines and derivatives were synthesized and assayed against purified NOS isoforms. 5-Cyano compounds are especially potent and selective rat and human nNOS inhibitors. Activity and selectivity are mediated by the binding of the cyano group to a new auxiliary pocket in nNOS. Potency was enhanced by methylation of the quinoline and by introduction of simple chiral moieties, resulting in a combination of hydrophobic and auxiliary pocket effects that yielded high (∼500-fold) n/e selectivity. Importantly, the Caco-2 assay also revealed improved membrane permeability over previous compounds.

摘要

神经元型一氧化氮合酶(nNOS)抑制是治疗神经退行性疾病的一种有前景的策略,但nNOS抑制剂的开发常常受到不良药代动力学的阻碍。我们之前开发了一类可透过细胞膜的2-氨基喹啉抑制剂,后来重新构建了骨架以减少脱靶结合。然而,所得化合物的通透性降低、人nNOS活性低且对人eNOS的选择性低。在本研究中,合成了5-取代苯基醚连接的氨基喹啉及其衍生物,并针对纯化的一氧化氮合酶同工型进行了测定。5-氰基化合物是特别有效的大鼠和人nNOS选择性抑制剂。活性和选择性是由氰基与nNOS中新的辅助口袋结合介导的。通过喹啉甲基化和引入简单手性部分增强了效力,产生了疏水作用和辅助口袋效应的组合,从而产生了高(约500倍)的n/e选择性。重要的是,Caco-2试验还显示,与之前的化合物相比,膜通透性有所提高。

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