a College of Pharmacy and Research Institute of Pharmaceutical Sciences , Seoul National University , Seoul , Republic of Korea.
b College of Pharmacy and Integrated Research Institute for Drug Development , Dongguk University-Seoul , Gyeonggi-do , Republic of Korea.
Nat Prod Res. 2019 Jun;33(12):1691-1698. doi: 10.1080/14786419.2018.1431632. Epub 2018 Jan 31.
One new furylhydroquinone derivative () and seven known compounds (-) were isolated from the roots of Sieb. et Zucc (Boraginaceae). The structure of was elucidated by extensive spectroscopic methods using NMR and MS. The absolute configuration of shikonofuran J () 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 () and uridine () remarkably down-regulated the TNF-α-induced synthesis of interleukin-6 (IL-6), a pro-inflammatory cytokine associated with cutaneous inflammation, in HaCaT cells.
从 Sieb. et Zucc(紫草科)的根部分离得到一种新的呋喃并氢醌衍生物()和七种已知化合物(-)。通过使用 NMR 和 MS 的广泛光谱方法阐明了的结构。通过与预测的 ECD 光谱的比较实验 ECD,明确确定了 shikonofuran J()的绝对构型。所有分离物均测试了它们对 TNF-α刺激的 HaCaT 细胞中 IL-6 产生的抑制活性。发现 gracicleistanthoside()和尿苷()显著下调 TNF-α诱导的与皮肤炎症相关的促炎细胞因子白细胞介素-6(IL-6)在 HaCaT 细胞中的合成。