腺苷A2A受体
腺苷
化学
腺苷受体
细胞外
受体
腺苷A3受体
腺苷A2B受体
腺苷A1受体
药理学
生物化学
立体化学
兴奋剂
生物
作者
Manuela Jörg,Jeremy Shonberg,Frankie S. Mak,Neil D. Miller,Elizabeth Yuriev,Peter J. Scammells,Ben Capuano
标识
DOI:10.1016/j.bmcl.2013.03.070
摘要
Growing evidence has suggested a role in targeting the adenosine A2A receptor for the treatment of Parkinson's disease. The literature compounds KW 6002 (2) and ZM 241385 (5) were used as a starting point from which a series of novel ligands targeting the adenosine A2A receptor were synthesized and tested in a recombinant human adenosine A2A receptor functional assay. In order to further explore these molecules, we investigated the biological effects of assorted linkers attached to different positions on selected adenosine A2A receptor antagonists, and assessed their potential binding modes using molecular docking studies. The results suggest that linking from the phenolic oxygen of selected adenosine A2A receptor antagonists is relatively well tolerated due to the extension towards extracellular space, and leads to the potential of attaching further functionality from this position.
科研通智能强力驱动
Strongly Powered by AbleSci AI