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2-氟-N-(3-氟-4-(5-((4-吗啉丁基)氨基)-1,3,4-恶二唑-2-基)苯基)苯甲酰胺的发现,一种 alpha-7 烟碱型乙酰胆碱受体的完全激动剂,在认知增强的新物体识别模型中显示出疗效。

The discovery of 2-fluoro-N-(3-fluoro-4-(5-((4-morpholinobutyl)amino)-1,3,4-oxadiazol-2-yl)phenyl)benzamide, a full agonist of the alpha-7 nicotinic acetylcholine receptor showing efficacy in the novel object recognition model of cognition enhancement.

机构信息

Neurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, New Frontiers Science Park, Harlow, Essex, UK.

出版信息

Bioorg Med Chem Lett. 2012 May 15;22(10):3531-4. doi: 10.1016/j.bmcl.2012.03.062. Epub 2012 Mar 21.

Abstract

A series of α7 nicotinic acetylcholine receptor full agonists with a 1,3,4-oxadiazol-2-amine core has been discovered. Early lead 1 was found to have a limited therapeutic index with respect to its potential for cardiovascular side effects. Further optimisation of this series led to the identification of 22 a potent full agonist showing efficacy at a dose of 0.1mg/kg in the novel object recognition model of cognition enhancement. Comparison of 1 with 22 demonstrated the latter to have an improved oral pharmacokinetic profile and cardiovascular therapeutic index.

摘要

我们发现了一系列以 1,3,4-恶二唑-2-胺为核心的α7 烟碱型乙酰胆碱受体全激动剂。早期先导化合物 1 由于其潜在的心血管副作用而显示出有限的治疗指数。进一步优化该系列化合物,得到了 22,它是一种有效的全激动剂,在认知增强的新型物体识别模型中,剂量为 0.1mg/kg 时具有疗效。1 与 22 的比较表明,后者具有改善的口服药代动力学特征和心血管治疗指数。

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