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Tetrahydropyrazolo[4,3-c]pyridine derivatives as potent and peripherally selective cannabinoid-1 (CB1) receptor inverse agonists

机译:四氢吡唑并[4,3-c]吡啶衍生物作为有效的和周边选择性大麻素-1(CB1)受体反向激动剂

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摘要

Peripherally restricted CB1 receptor inverse agonists hold potential as useful therapeutics to treat obesity and related metabolic diseases without causing undesired CNS-mediated adverse effects. We identified a series of tetrahydropyrazolo[4,3-c]pyridine derivatives as potent and highly peripherally selective CB1 receptor inverse agonists. This discovery was achieved by introducing polar functional groups into the molecule, which increase the topological polar surface area and reduce its brain-penetrating ability. (C) 2016 Elsevier Ltd. All rights reserved.
机译:周围受限的CB1受体反向激动剂具有潜力,可作为治疗肥胖症和相关代谢疾病的有用疗法,而不会引起不良的CNS介导的不良反应。我们确定了一系列的四氢吡唑并[4,3-c]吡啶衍生物作为有效的和高度外围选择性的CB1受体反向激动剂。该发现是通过将极性官能团引入分子而实现的,该官能团增加了拓扑极性表面积并降低了其穿透大脑的能力。 (C)2016 Elsevier Ltd.保留所有权利。

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