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从苯并氮䓬类组胺 H3 受体拮抗剂中鉴定临床候选药物。

Identification of clinical candidates from the benzazepine class of histamine H3 receptor antagonists.

机构信息

GlaxoSmithKline R&D, Neurology Centre of Excellence for Drug Discovery, Harlow, Essex CM19 5AW, United Kingdom.

出版信息

Bioorg Med Chem Lett. 2013 Dec 15;23(24):6890-6. doi: 10.1016/j.bmcl.2013.09.090. Epub 2013 Oct 5.

Abstract

This Letter describes the discovery of GSK189254 and GSK239512 that were progressed as clinical candidates to explore the potential of H3 receptor antagonists as novel therapies for the treatment of Alzheimer's disease and other dementias. By carefully controlling the physicochemical properties of the benzazepine series and through the implementation of an aggressive and innovative screening strategy that employed high throughput in vivo assays to efficiently triage compounds, the medicinal chemistry effort was able to rapidly progress the benzazepine class of H3 antagonists through to the identification of clinical candidates with robust in vivo efficacy and excellent developability properties.

摘要

这封信描述了 GSK189254 和 GSK239512 的发现,它们被推进为临床候选药物,以探索 H3 受体拮抗剂作为治疗阿尔茨海默病和其他痴呆症的新型疗法的潜力。通过仔细控制苯并氮杂䓬系列的物理化学性质,并通过实施积极创新的筛选策略,利用高通量体内测定法有效地对化合物进行分类,药物化学工作能够迅速将苯并氮杂䓬类 H3 拮抗剂推进到具有强大体内疗效和优良开发性能的临床候选药物的鉴定。

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