School of Pharmacy, Xinxiang Medical University, Xinxiang, 453003, P. R. China.
Chem Biodivers. 2020 Jul;17(7):e2000238. doi: 10.1002/cbdv.202000238. Epub 2020 Jun 23.
Six new eudesmane-type sesquiterpene derivatives, artemargyinins A-F were isolated from the leaves of Artemisia argyi. Their structures were elucidated based on the extensive analysis of spectroscopic data. Artemargyinins A-F feature a lactone ring-opening eudesmane-type sesquiterpene with an isoprenoid group at C(8). All compounds were tested for their inhibitory effects on lipopolysaccharide-induced nitric oxide (NO) production in RAW264.7 macrophages. Artemargyinins A-F showed more potent NO production inhibitory activity with IC values ranging from 7.66±0.53 to 61.19±2.54 μM than the positive control quercetin (IC =74.34±1.39 μM). Among them, artemargyinins C and D exhibited strong inhibitory activity with IC values of 8.08±0.21 and 7.66±0.53 μM, respectively.
从艾草的叶子中分离得到了六种新的半日花烷型倍半萜衍生物,即青蒿因 A-F。根据光谱数据分析,确定了它们的结构。青蒿因 A-F 的特征是内酯环开裂的半日花烷型倍半萜,在 C(8) 位具有异戊烯基。所有化合物均测试了其对 RAW264.7 巨噬细胞中脂多糖诱导的一氧化氮(NO)产生的抑制作用。青蒿因 A-F 显示出比阳性对照槲皮素(IC=74.34±1.39 μM)更强的 NO 产生抑制活性,IC 值范围为 7.66±0.53 至 61.19±2.54 μM。其中,青蒿因 C 和 D 表现出较强的抑制活性,IC 值分别为 8.08±0.21 和 7.66±0.53 μM。