兴奋剂
哮喘
慢性阻塞性肺病
毒蕈碱乙酰胆碱受体
受体
B2受体
敌手
药理学
G蛋白偶联受体
β2肾上腺素能受体
医学
生物信息学
生物
内科学
缓激肽
作者
Gang Xing,Ce Yi,Peiyuan Dou,Zhengxing Zhi,Bin Lin,Maosheng Cheng
标识
DOI:10.1080/13543776.2021.1865312
摘要
Introduction The β2 adrenergic receptor (β2AR) is a member of G protein-coupled receptors (GPCRs) that mediate the majority of cellular responses to external stimuli. The agonists can cause smooth muscle relaxation; therefore, many β2AR agonists have been developed especially for the treatment of pulmonary disorders such as asthma and chronic obstructive pulmonary disease (COPD). Many new natural and synthetic compounds have been discovered and developed as novel β2AR agonists over the past 5 years.Areas covered This review offers an update for the development of β2AR agonists in the patents published from 2015 to 2020, including new natural and synthetic compounds for the treatment of asthma and COPD. In particular, the latest patents about compounds possessing both muscarinic receptor antagonist and β2 adrenergic receptor agonist activity are reviewed.Expert opinion β2AR agonists have been developed extensively for the treatment of asthma and COPD. In the past 5 years, novel agonists from both natural sources and synthetic methods were intensively developed. Compounds possessing both muscarinic receptor antagonist and β2AR agonist activity represent a new trend in this area because they are possibly able to act together in a synergistic fashion, therefore, relieve the symptoms of patients through two distinct mechanisms.
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