Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.
Key Laboratory of New Drugs (Traditional Chinese Medicine) for Respiratory Viral Diseases of Yunnan Province, Kunming 650500, China.
Molecules. 2023 Nov 23;28(23):7726. doi: 10.3390/molecules28237726.
An undescribed diterpene, stellerterpenoid A (), and two undescribed sesquiterpenoids, stellerterpenoids B and C (-), together with six known compounds, prostratin () stelleraguaianone B (), chamaejasnoid A (), auranticanol L (), wikstronone C (), and oleodaphnone (), were isolated from the roots of L. Their structures were elucidated by extensive spectroscopic data (1D, 2D NMR, IR, UV, and HR-ESI-MS). The absolute configuration of - was elucidated based on ECD calculation. Among them, stellerterpenoid A was a rare 13, 14-seco nortigliane diterpenoid and stellerterpenoid B was a guaiacane-type sesquiterpenoid with an unusual 1, 2-diketone moiety. The known stelleraguaianone B () exhibited moderate activity for suppressing NO production in lipopolysaccharide (LPS)-treated RAW 264.7 macrophages cells with an IC value of 24.76 ± 0.4 μM. None of the compounds showed anti-influenza virus or anti-tumor activity in vitro.
一种新的二萜类化合物,海鞘萜烯 A(),以及两种新的倍半萜类化合物,海鞘萜烯 B 和 C(),与 6 种已知化合物一起,从 L. 的根部分离出来。通过广泛的光谱数据(1D、2D NMR、IR、UV 和 HR-ESI-MS)阐明了它们的结构。根据 ECD 计算确定了 - 的绝对构型。其中,海鞘萜烯 A 是一种罕见的 13、14-断北里烷二萜,海鞘萜烯 B 是一种具有不寻常 1,2-二酮部分的愈创木烷型倍半萜。已知的海鞘烷酮 B()对脂多糖(LPS)处理的 RAW 264.7 巨噬细胞中 NO 产生的抑制活性具有中等活性,IC 值为 24.76±0.4 μM。这些化合物在体外均无抗流感病毒或抗肿瘤活性。