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作 者:Rihan Xie Linsheng Li Xiaona Fan Jiachen Zi
机构地区:[1]College of Pharmacy,Ji'nan University,Guangzhou 510632,China [2]School of Medicine,Ji'nan University,Guangzhou 510632,China
出 处:《Chinese Chemical Letters》2020年第2期431-433,共3页中国化学快报(英文版)
基 金:financially supported by the National Natural Science Foundation of China(No.81673530);Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program(No.2017BT01Y036)。
摘 要:A novel meroterpenoid,euphoractone(1),was isolated from the extracts of the roots of Euphorbia fischeriana Steud.Its structure was determined by spectroscopic methods and X-ray crystallography.1 possesses an unusual ent-abietane-phloroglucinol skeleton.The plausible biosynthetic pathway for 1 was proposed.1 showed inhibitory activities against human lung cancer H23 and H460 cells with the IC_(50)values of 21.07±3.54 and 20.91±4.07 μmol/L.A novel meroterpenoid,euphoractone(1),was isolated from the extracts of the roots of Euphorbia fischeriana Steud.Its structure was determined by spectroscopic methods and X-ray crystallography.1 possesses an unusual ent-abietane-phloroglucinol skeleton.The plausible biosynthetic pathway for 1 was proposed.1 showed inhibitory activities against human lung cancer H23 and H460 cells with the IC50values of 21.07±3.54 and 20.91±4.07 μmol/L.
关 键 词:EUPHORBIA fischeriana Meroterpenoid ent-Abietane PHLOROGLUCINOL Euphoractone Cytotoxicity
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