药物发现
多巴胺受体D3
计算生物学
合理设计
神经科学
药理学
G蛋白偶联受体
受体
多巴胺受体
生物
医学
多巴胺
计算机科学
生物信息学
生物化学
遗传学
作者
Rita Maria Concetta Di Martino,Andrea Cavalli,Giovanni Bottegoni
标识
DOI:10.1080/13543776.2022.2049240
摘要
Compelling evidence identified D3 dopamine receptor (D3R) as a suitable target for therapeutic intervention on CNS-associated disorders, cancer, and other conditions. Several efforts have been made toward developing potent and selective ligands for modulating signaling pathways operated by these GPCRs. The rational design of D3R ligands endowed with a pharmacologically relevant profile has traditionally not encountered much support from computational methods due to a very limited knowledge of the receptor structure and of its conformational dynamics. Recent progress in structural biology will change this state of affairs in the next decade.This review provides an overview of the recent (2014-2020) patent literature on novel classes of D3R ligands developed within the framework of CNS-related diseases, cancer, and additional conditions. When possible, an in-depth description of both in vitro and in vivo generated data is presented. New therapeutic applications of known molecules with activity at D3R are discussed.Building on current knowledge, future D3R-focused drug discovery campaigns will be propelled by a combination of unprecedented availability of structural information with advanced computational and analytical methods. The design of D3R ligands with the sought activity, efficacy, and selectivity profile will become increasingly more streamlined.
科研通智能强力驱动
Strongly Powered by AbleSci AI