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组胺H3受体拮抗剂进入临床应用。

Histamine H3 receptor antagonists go to clinics.

作者信息

Sander Kerstin, Kottke Tim, Stark Holger

机构信息

Johann Wolfgang Goethe-Universität Frankfurt am Main, Institut für Pharmazeutische Chemie, Frankfurt/Main, Germany.

出版信息

Biol Pharm Bull. 2008 Dec;31(12):2163-81. doi: 10.1248/bpb.31.2163.

Abstract

Within the recent years novel lead optimisations for histamine H(3) receptor antagonists made their way from bench to bedside. Structure-activity relationships, cross-affinities and side effects as well as pharmacokinetic profiling will be discussed on selected promising compound series. Due to diversity in potential therapeutic applications and in some cases a controversial debate, different indications will be highlighted with the potential and the problems of the test compounds, e.g. sleep-wake disorders, attention-deficient hyperactivity disorder, epilepsy, cognitive impairment, schizophrenia, obesity and neuropathic pain. First data published on clinical trials phase II (IIb) are presented showing proof of concept of H(3) receptor antagonists in narcolepsy and photo-induced epilepsy.

摘要

近年来,组胺H(3)受体拮抗剂新型先导物优化已从实验室走向临床。将针对选定的有前景的化合物系列讨论构效关系、交叉亲和力和副作用以及药代动力学特征。由于潜在治疗应用的多样性以及在某些情况下存在争议性辩论,将重点介绍不同适应症以及受试化合物的潜力和问题,例如睡眠-觉醒障碍、注意力缺陷多动障碍、癫痫、认知障碍、精神分裂症、肥胖症和神经性疼痛。文中展示了已发表的关于II期(IIb期)临床试验的首批数据,证明了H(3)受体拮抗剂在发作性睡病和光诱发性癫痫中的概念验证。

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