ALKYL 3-((2-AMIDOETHYL)AMINO)-8-AZABICYCLO[3.2.1]OCTANE-8-CARBOXYLATE ANALOGS AS SELECTIVE M1 AGONISTS AND METHODS OF MAKING AND USING SAME
申请人:Conn P. Jeffrey
公开号:US20110172227A1
公开(公告)日:2011-07-14
In one aspect, the invention relates to compounds having a general structure:
which are useful as selective allosteric or bitopic agonists of the M
1
muscarinic receptor; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of using the compounds, for example, in treating neurodegenerative diseases, including Alzheimer's Disease. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
在一个方面,该发明涉及具有一般结构的化合物:
这些化合物可用作M1-肌胆碱受体的选择性变构或双拓扑激动剂;制备这些化合物的合成方法;包括这些化合物的药物组合物;以及使用这些化合物的方法,例如,在治疗神经退行性疾病,包括阿尔茨海默病。本摘要旨在作为在特定领域进行搜索的扫描工具,并不意味着对本发明的限制。