Wei Hong-Li, Zhao Yao-Peng, Wang Ji-Xia, Han Yang, Li Hao, Zhou Han, Hou Tao, Wang Chang-Jian, Yao Yu-Min, Zhang Xiu-Li, Liu Yan-Fang, Liang Xin-Miao
Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, People's Republic of China.
Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, People's Republic of China; University of Chinese Academy of Sciences, Beijing 100049, People's Republic of China.
Bioorg Chem. 2022 Oct;127:106027. doi: 10.1016/j.bioorg.2022.106027. Epub 2022 Jul 13.
A total of 33 structurally diverse isoquinoline alkaloids were isolated from the rhizomes of Menispermum dauricum, including seventeen benzylisoquinoline analogues (menisperdaurines A-Q, 1-17), five protoberberine analogues (menisperdaurines R-V, 18-22), a quaternary phenanthrene alkaloid (menisperdaurine W, 23) and ten known compounds (24-33). Compound structures, including absolute configurations, were determined by extensive spectroscopic methods, quantum chemical calculations of chemical shifts, and calculated and experimental electronic circular dichroism (ECD) data. Compounds 1-5 were glycosidic benzylisoquinolines with glucose moieties attached at the C-12 position. Compound 8 was the first example that was isolated from the rhizomes of Menispermum dauricum, benzylisoquinoline and an aromatic unit connected by a sugar bridge. Compounds were evaluated for their inhibitory effects on the dopamine D1 receptor. Compounds 1, 8, 21, 24 and 29 showed potent D1 antagonistic activities, with IC values ranging from 1.0 to 4.5 μM. Compound 1 exhibited the highest antagonistic activity with an IC value of 1.0 ± 0.2 μM.
从蝙蝠葛根茎中总共分离出33种结构多样的异喹啉生物碱,包括17种苄基异喹啉类似物(蝙蝠葛碱A - Q,1 - 17)、5种原小檗碱类似物(蝙蝠葛碱R - V,18 - 22)、一种季铵型菲生物碱(蝙蝠葛碱W,23)和10种已知化合物(24 - 33)。通过广泛的光谱方法、化学位移的量子化学计算以及计算和实验电子圆二色光谱(ECD)数据确定了化合物结构,包括绝对构型。化合物1 - 5是在C - 12位带有葡萄糖部分的糖苷化苄基异喹啉。化合物8是从蝙蝠葛根茎中分离得到的首个例子,即苄基异喹啉与一个芳香单元通过糖桥相连。评估了这些化合物对多巴胺D1受体的抑制作用。化合物1、8、21、24和29表现出强效的D1拮抗活性,IC值范围为1.0至4.5 μM。化合物1表现出最高的拮抗活性,IC值为1.0 ± 0.2 μM。