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南海软珊瑚来源结构多样的二萜

Structurally Diverse Diterpenes from the South China Sea Soft Coral .

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 Life Sciences, Shanghai Normal University, 100 Guilin Road, Shanghai 200234, China.

出版信息

Mar Drugs. 2023 Jan 20;21(2):69. doi: 10.3390/md21020069.

DOI:10.3390/md21020069
PMID:36827110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9960596/
Abstract

The present investigation of the South China Sea soft coral resulted in the discovery of six new polyoxygenated diterpenes, namely sartrocheliols A-E (, , -) along with four known ones, , , , and . Based on extensive spectroscopic data analysis, sartrocheliol A () was identified as an uncommon capnosane diterpene, while sartrocheliols B-E (, -) were established as cembrane diterpenes. They displayed diverse structural features not only at the distinctly different carbon frameworks but also at the various types of heterocycles, including the epoxide, γ-lactone, furan, and pyran rings. Moreover, their absolute configurations were determined by a combination of quantum mechanical-nuclear magnetic resonance (QM-NMR) approach, modified Mosher's method, and X-ray diffraction analysis. In the anti-tumor bioassay, compound exhibited moderate cytotoxic activities against A549, H1975, MDA-MB-231, and H1299 cells with the IC values ranging from 26.3 to 47.9 μM.

摘要

本研究对南海软珊瑚进行了调查,从中发现了六种新的多氧化二萜,分别为 sartrocheliols A-E(1-6),以及四种已知的化合物 、 、 、 。通过广泛的光谱数据分析,确定 sartrocheliol A(1)为一种不常见的碳烷二萜,而 sartrocheliols B-E(2-6)则被确定为枞烷二萜。它们不仅在明显不同的碳骨架上,而且在各种类型的杂环,包括环氧化物、γ-内酯、呋喃和吡喃环上,显示出不同的结构特征。此外,它们的绝对构型是通过量子力学-核磁共振(QM-NMR)方法、改进的 Mosher 方法和 X 射线衍射分析相结合确定的。在抗肿瘤生物测定中,化合物 6 对 A549、H1975、MDA-MB-231 和 H1299 细胞表现出中等的细胞毒性活性,IC 值范围为 26.3-47.9 μM。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/c51e24d85e2a/marinedrugs-21-00069-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/226d6a1ef408/marinedrugs-21-00069-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/3958f5a0e6c9/marinedrugs-21-00069-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/9ce5bc204b76/marinedrugs-21-00069-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/cfffc3881cf9/marinedrugs-21-00069-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/0dd170011919/marinedrugs-21-00069-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/14e824b08cc8/marinedrugs-21-00069-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/09fdac2d97ae/marinedrugs-21-00069-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/c51e24d85e2a/marinedrugs-21-00069-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/226d6a1ef408/marinedrugs-21-00069-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/3958f5a0e6c9/marinedrugs-21-00069-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/9ce5bc204b76/marinedrugs-21-00069-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/cfffc3881cf9/marinedrugs-21-00069-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/0dd170011919/marinedrugs-21-00069-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/14e824b08cc8/marinedrugs-21-00069-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/09fdac2d97ae/marinedrugs-21-00069-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228f/9960596/c51e24d85e2a/marinedrugs-21-00069-g008.jpg

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