哈卡特
消炎药
紫草科
化学
立体化学
肿瘤坏死因子α
传统医学
生物化学
药理学
生物
植物
医学
免疫学
体外
作者
Jongmin Ahn,Hee‐Sung Chae,Young‐Won Chin,Jinwoong Kim
标识
DOI:10.1080/14786419.2018.1431632
摘要
One new furylhydroquinone derivative (1) and seven known compounds (2-8) were isolated from the roots of Lithospermum erythrorhizon Sieb. et Zucc (Boraginaceae). The structure of 1 was elucidated by extensive spectroscopic methods using NMR and MS. The absolute configuration of shikonofuran J (1) was unambiguously determined by aid of comparison experimental ECD with predicted ECD spectra. All the isolates were tested for their inhibitory activities against IL-6 production in HaCaT cells stimulated by tumor necrosis factor (TNF)-α. It was found that gracicleistanthoside (5) and uridine (7) remarkably down-regulated the TNF-α-induced synthesis of interleukin-6 (IL-6), a pro-inflammatory cytokine associated with cutaneous inflammation, in HaCaT cells.
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