Neurosciences Centre of Excellence for Drug Discovery, GlaxoSmithKline, New Frontiers Science Park, Harlow, Essex, UK.
Bioorg Med Chem Lett. 2012 May 15;22(10):3531-4. doi: 10.1016/j.bmcl.2012.03.062. Epub 2012 Mar 21.
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.
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。