School of Pharmacy, Guiyang Medical University, Guiyang, China.
Nat Prod Res. 2011 Sep;25(15):1418-22. doi: 10.1080/14786410802496911. Epub 2011 Jul 8.
In a bioassay-guided search for acetylcholinesterase (AChE) inhibitors from Chinese natural resources, eight isoquinoline alkaloids, tetrahydropalmatine (1), corydaline (2), protopine (3), berberine (4), palmatine (5), jatrorrhizine (6), coptisine (7) and dehydrocorydaline (8), were isolated from the methanolic extract of the tubers of Corydalis yanhusuo. Structures of these compounds were identified by spectroscopic techniques. Compounds 4-8 inhibited AChE activity in a dose-dependent manner, and the IC₅₀ values were 0.47 ± 0.01, 0.74 ± 0.06, 2.08 ± 0.09, 1.01 ± 0.03 and 0.62 ± 0.05 µM, respectively. Structure-activity relationship analysis suggested that aromatisation at ring C, as well as substitutions at C-2, C-3, C-9, C-10 and C-13 affect the AChE activity of protoberberine alkaloids.
在一项针对中国天然资源中乙酰胆碱酯酶 (AChE) 抑制剂的生物测定指导的研究中,从延胡索的块茎甲醇提取物中分离得到了 8 种异喹啉生物碱,分别为四氢巴马汀(1)、紫堇碱(2)、原阿片碱(3)、小檗碱(4)、掌叶防己碱(5)、延胡索乙素(6)、黄连碱(7)和脱氢紫堇碱(8)。通过光谱技术鉴定了这些化合物的结构。化合物 4-8 呈剂量依赖性抑制 AChE 活性,IC₅₀ 值分别为 0.47 ± 0.01、0.74 ± 0.06、2.08 ± 0.09、1.01 ± 0.03 和 0.62 ± 0.05 μM。构效关系分析表明,C 环芳构化以及 C-2、C-3、C-9、C-10 和 C-13 的取代会影响原小檗碱类生物碱的 AChE 活性。