Novel GlyT1 inhibitor chemotypes by scaffold hopping. Part 2: Development of a [3.3.0]-based series and other piperidine bioisosteres
摘要:
This Letter describes the development and SAR of a novel series of GlyT1 inhibitors derived from a scaffold hopping approach, in lieu of an HTS campaign, which provided intellectual property position. Members within this new [3.3.0]-based series displayed excellent GlyT1 potency, selectivity, free fraction, and modest CNS penetration. Moreover, enantioselective GlyT1 inhibition was observed, within this novel series and a number of other piperidine bioisosteric cores. (C) 2014 Elsevier Ltd. All rights reserved.
[EN] PROGRANULIN MODULATORS AND METHODS OF USING THE SAME<br/>[FR] MODULATEURS DE LA PROGRANULINE ET LEURS PROCÉDÉS D'UTILISATION
申请人:ARKUDA THERAPEUTICS
公开号:WO2020252222A1
公开(公告)日:2020-12-17
Provided herein are compounds that modulate progranulin and methods of using the compounds in progranulin-associated disorders, such as Frontotemporal dementia (FTD).
本文件提供了调节颗粒蛋白的化合物及其在颗粒蛋白相关疾病中的使用方法,例如额颞痴呆(FTD)。
Azabicyclic compounds are central nervous system active agents
申请人:——
公开号:US20040044029A1
公开(公告)日:2004-03-04
Compounds of formula (I)
1
are novel CNS active agents that are useful for treating pain and for treating other disorders associated with the cholinergic system.