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扩展来自软珊瑚米氏棘软珊瑚的萜类记录。

Extending the Record of Terpenes from Soft Coral Sarcophyton mililatensis.

作者信息

Yang Min, Ge Zeng-Yue, Chen Zi-Hui, Yao Li-Gong, Liang Lin-Fu, Guo Yue-Wei

机构信息

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.

College of Materials Science and Engineering, Central South University of Forestry and Technology, 498 South Shaoshan Road, Changsha, 410004, China.

出版信息

Chem Biodivers. 2023 Apr;20(4):e202300267. doi: 10.1002/cbdv.202300267. Epub 2023 Apr 3.

Abstract

In the present study, a new polyoxygenated cembranoid named sarcomililatol H (1) as well as six known terpenes 2-7 with different skeletons were isolated from South China Sea soft coral Sarcophyton mililatensis. Based on the comprehensive analyses of 1D and 2D NMR spectroscopic data, the structure of the new compound 1 was established. This new cembranoid was characterized by the presence of the rarely encountered tetrahydropyran ring with the ether linkage across C-2 and C-12. By applying the time-dependent density functional theory electronic circular dichroism (TDDFT ECD) approach, the absolute configuration of sarcomililatol H (1) was determined. All of the isolates were subjected to the anti-inflammatory and anti-tumor bioassays. However, none of them was active in these evaluations. Additionally, the preliminary virtual screening of inhibitory against SARS-CoV-2 by molecular docking showed that diterpene 1 could be regarded as a SARS-CoV-2 main protease (M ) inhibitor (binding energy: -7.63 kcal/mol). The discovery of these terpenes has expanded the chemical diversity and complexity of terpenes from the species S. mililatensis.

摘要

在本研究中,从中国南海软珊瑚密枝肉芝软珊瑚(Sarcophyton mililatensis)中分离出一种名为肉芝软珊瑚醇H(1)的新型多氧化柳珊瑚烷类化合物以及六种具有不同骨架的已知萜类化合物2 - 7。基于对一维和二维核磁共振光谱数据的综合分析,确定了新化合物1的结构。这种新的柳珊瑚烷类化合物的特征在于存在罕见的四氢吡喃环,其在C - 2和C - 12之间具有醚键连接。通过应用含时密度泛函理论电子圆二色光谱(TDDFT ECD)方法,确定了肉芝软珊瑚醇H(1)的绝对构型。所有分离物都进行了抗炎和抗肿瘤生物活性测试。然而,它们在这些评估中均无活性。此外,通过分子对接对抑制新型冠状病毒(SARS-CoV-2)的初步虚拟筛选表明,二萜1可被视为一种新型冠状病毒主要蛋白酶(Mpro)抑制剂(结合能:-7.63 kcal/mol)。这些萜类化合物的发现扩展了密枝肉芝软珊瑚中萜类化合物的化学多样性和复杂性。

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