去甲二氢愈创木酸
化学
抑制性突触后电位
立体化学
生物化学
生物
酶
脂氧合酶
神经科学
作者
Jongmin Ahn,Yihua Pei,Hee‐Sung Chae,Seong-Hwan Kim,Young‐Mi Kim,Young Hee Choi,Joongku Lee,Minsun Chang,Yun Seon Song,Roberto Rodríguez,Dong‐Chan Oh,Jinwoong Kim,Sangho Choi,Sang Woo Joo,Young‐Won Chin
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2018-01-31
卷期号:23 (2): 302-302
被引量:2
标识
DOI:10.3390/molecules23020302
摘要
Bioactivity-guided fractionation for the stems of leaves of Larrea nitida Cav., using interleukin-6 (IL-6) inhibitory assay in human mast cells (HMC-1), led to the isolation of three new compounds with an unprecedented skeleton in nature (1–3) and three known compounds (4–6). Their structures were elucidated through extensive spectroscopic analysis. The three new compounds were elucidated as two new spiroketones, nitidaones A (1), and B (2) and one new biphenyl analog, nitidaol (3). The known compounds were identified as nordihydroguaiaretic acid (4), 7,3′,4′-tri-O-methylquercetin (5) and ayanin (6). All the isolates were tested for their inhibitory activity against IL-6 production in HMC-1 cells. Of them, compounds 1, 3–6 showed potent anti-inflammatory activity, with IC50 values of 12.8, 17.5, 14.9, 22.9, and 17.8 µM, respectively.
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