In one aspect, the invention relates to substituted imidazopyridine and triazolopyridine analogs, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M1 (mAChR M1); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the disclosed compounds and compositions. 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,该发明涉及替代
咪唑吡啶和三唑
吡啶类似物,它们的衍
生物以及相关化合物,这些化合物可用作肌
胆碱受体M1(mAChR M1)的正向变构调节剂;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;以及使用所披露的化合物和组合物治疗与肌
胆碱受体功能障碍相关的神经和精神疾病的方法。本摘要旨在作为在特定领域进行搜索的扫描工具,并不旨在限制本发明。