The Discovery of LML134, a Histamine H3 Receptor Inverse Agonist for the Clinical Treatment of Excessive Sleep Disorders
作者:Thomas Troxler、Dominik Feuerbach、Xuechun Zhang、Charles R. Yang、Bharat Lagu、Mark Perrone、Tie‐Lin Wang、Karin Briner、Mark G. Bock、Yves P. Auberson
DOI:10.1002/cmdc.201900176
日期:2019.7.3
Histamine H3 receptor (H3R) inverse agonists that have been in clinical trials for the treatment of excessive sleep disorders, have been plagued with insomnia as a mechanism‐based side effect. We focused on the identification of compounds that achieve high receptor occupancy within a short time, followed by rapid disengagement from the receptor, a target profile that could provide therapeutic benefits
在临床试验中用于治疗过度睡眠障碍的组胺H3受体(H3R)反向激动剂已因失眠而困扰,这是一种基于机制的副作用。我们专注于鉴定可在短时间内实现高受体占有率,然后迅速与受体脱离的目标化合物,该目标谱可提供治疗益处而不会出现失眠的不良副作用。本文介绍了导致发现1-(1-甲基-6-氧代-1,6-二氢哒嗪-3-基)哌啶-4-基4-环丁基哌嗪-1-羧酸酯的优化工作(18 b,LML134 )。