丁酰胆碱酯酶
乙酰胆碱酯酶
胆碱酯酶
化学
胆碱能的
阿切
乙酰胆碱
IC50型
抑制性突触后电位
药理学
生物化学
立体化学
酶
体外
心理学
神经科学
生物
作者
Rangaswamy Roopashree,Toreshettahally R. Swaroop,Swamy Jagadish,Chakrabhavi Dhananjaya Mohan,Kanchugarakoppal S. Rangappa
标识
DOI:10.2174/1570180811666140704171902
摘要
Cholinesterase plays a vital role in the decline of cholinergic transmission and thus can contribute to the development of Alzheimer’s disease (AD). Thus, compounds that can inhibit acetylcholinesterase (AChe) and butyrylcholinesterase (BuChe) are the potential drugs for the treatment of AD. A series of novel pyrrolopyrimidine derivatives was synthesized and evaluated for their inhibitory activity against cholinesterase by Ellman method. Among the ten newly synthesized compounds, 4-(4-((4-(difluoromethoxy)phenyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)benzoate was the most potent molecule identified with the IC50 values of 18 µM and 17 µM on AChe and BuChe respectively. Keywords: Acetylcholinesterase, alzheimer’s disease, butyrylcholinesterase, cholinergic transmission, inhibition, pyrrolopyrimidine.
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