三萜胆碱酯酶抑制剂可能改善帕金森病患者的步态障碍

Niels V. Heise, Jördis-Ann Schüler, Torje E. Orlamünde, Benjamin Brandes, H. Deigner, A. Al‐Harrasi, R. Csuk
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引用次数: 0

摘要

帕金森病(PD)是第二常见的神经退行性疾病。除了僵硬和震颤外,患者还常伴有步态障碍。用胆碱酯酶抑制剂(ChEI)治疗已被证明可以改善步态速度。因此,三萜酸齐墩果酸和熊果酸已被用作合成乙酰胆碱酯酶(AChE)和丁基胆碱酯酶(BChE)抑制剂的化合物的起始原料。母体化合物经异氰酸酯和胺类化合物乙酰化转化为一系列酰胺类化合物,同时异氰酸酯也被用作合成几种尿素衍生物的起始原料。与胆碱酯酶结合的化合物的筛选表明,它们是良好的到中度抑制剂,熊果酸衍生的异氰酸酯是一种较好的混合型双抑制剂,对两种酶都具有较好的抑制作用,其Ki值在低mM浓度范围内。实验数据与分子模拟计算的结果相吻合。此外,该化合物在水溶液中非常稳定,只需在50°C下几个小时就能脱羧水解成相应的胺。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Triterpenoid cholinesterase inhibitors that might improve gait disturbances in Parkinson's disease patients
: Parkinson's disease (PD) is the second most common neurodegenerative disease. Besides rigidity and tremor, patients often suffer from gait disturbance. Treatment with cholinesterase inhibitors (ChEI) has been shown to improve gait speed. Thus, the triterpene acids oleanolic acid and ursolic acid have been used as starting materials for the synthesis of compounds intended to act as inhibitors of the enzymes acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). The parent compounds were acetylated and converted via isocyanates and amines into a series of amides, while the isocyanates were also used as starting materials for the synthesis of several urea derivatives. Screening of the compounds with the cholinesterases showed them to be good to moderate inhibitors, with ursolic acid derived isocyanate being a superior mixed-type dual inhibitor for both enzymes holding Ki values in the low mM concentration range. The data from the experiments parallel the results from molecular modeling calculations. In addition, this compound is remarkably stable in an aqueous solution and undergoes decarboxylative hydrolysis to the corresponding amine only at 50 °C after several hours.
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