Alkaloid Dimers Isolated from Thalictrum baicalense Have Antitumor Activities
作者机构:Key Laboratory of Structure-Based Drug Design&DiscoveryMinistry of EducationShenyang Pharmaceutical UniversityShenyangLiaoning 110016China School of Traditional Chinese Materia MedicaShenyang Pharmaceutical UniversityShenyangLiaoning 110016China School of Pharmaceutical EngineeringShenyang Pharmaceutical UniversityShenyangLiaoning 110016China Wuya College of InnovationShenyang Pharmaceutical UniversityShenyangLiaoning 110016China
出 版 物:《Chinese Journal of Chemistry》 (中国化学(英文版))
年 卷 期:2022年第40卷第15期
页 面:1831-1841页
核心收录:
学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学]
基 金:This work was supported by the National Natural Science Foundationof China(No.82173715)
主 题:Thalictrum baicalense Heterodimeric isoquinoline alkaloid Thalifaberine-type ABI alkaloids Antitumor activity Apoptosis
摘 要:Comprehensive Summary A pair of heterodimeric isoquinoline alkaloid enantiomers,(+)thaliberberine A,five new thalifaberine-type aporphine-benzylisoquinoline(ABl)alkaloids,thalicultratines M-Q,and thirteen known analogues were isolated from the roots of Thalictrum baicalense *** *** structures were determined by extensive spectroscopic methods and ECD *** A featuring a novel carbon skeleton coupled by two different classes of isoquinoline alkaloids,protoberberine and phthalidoisoquinoline,represents the first natural product with the berberine skeleton substituted at *** biosynthetic routes of 1 are proposed.