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来自海南软珊瑚的具有非芳环氧杂环的海松烷二萜

Cembrane Diterpenes Possessing Nonaromatic Oxacycles from the Hainan Soft Coral .

机构信息

College of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004, China.

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zu Chong Zhi Road, Zhangjiang Hi-Tech Park, Shanghai 201203, China.

出版信息

Int J Mol Sci. 2023 Jan 19;24(3):1979. doi: 10.3390/ijms24031979.

Abstract

Documents on the chemical composition of the soft coral are sparse. The present investigation of the Hainan soft coral resulted in the discovery of six new cembrane diterpenes, sarcoxacyclols A-F (-) and four known analogs (-). Their structures were elucidated by extensive spectroscopic analysis along with a comparison with the data in current literature. The nonaromatic oxacycles in their structures were the rarely found tetrahydrofuran ether across C-1 and C-12 and tetrahydropyran ether across C-1 and C-11, respectively. Moreover, the absolute configuration of compound was established unambiguously by X-ray diffraction analysis using Ga Kα radiation ( = 1.34139 Å). Based on the biogenetical consideration, the absolute configurations of other five new compounds were tentatively assumed. Assessment of the bioactivity for these secondary metabolites revealed that compound exhibited significant tumor necrosis factor (TNF)- inhibitory activity (IC = 9.5 μmol/L), similar to the positive control dexamethasone (IC = 8.7 μmol/L), but no obvious cytotoxicity towards RAW264.7 cells (CC > 50 μmol/L). The preliminary molecular docking suggested the crucial roles of the hydroxyl and acetoxyl groups in the computational prediction of the binding mode between the diterpene and the protein.

摘要

关于软珊瑚化学成分的文献资料很少。本研究对海南软珊瑚进行了研究,发现了六种新的海鞘烷二萜,即 sarcoxacyclols A-F(-)和四种已知类似物(-)。通过广泛的光谱分析以及与当前文献数据的比较,确定了它们的结构。其结构中的非芳香环是在 C-1 和 C-12 之间的四氢呋喃醚和在 C-1 和 C-11 之间的四氢吡喃醚,这是很少见的。此外,通过使用 Ga Kα 辐射( = 1.34139 Å)的 X 射线衍射分析,明确确定了化合物的绝对构型。基于生物发生的考虑,暂定假设了其他五种新化合物的绝对构型。对这些次生代谢物的生物活性评估表明,化合物表现出显著的肿瘤坏死因子(TNF)抑制活性(IC = 9.5 μmol/L),与阳性对照地塞米松(IC = 8.7 μmol/L)相似,但对 RAW264.7 细胞无明显细胞毒性(CC > 50 μmol/L)。初步的分子对接表明,羟基和乙酰氧基在计算预测二萜与蛋白质之间的结合模式方面起着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7963/9915928/2b480cd8ce87/ijms-24-01979-g001.jpg

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