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来自柔指软珊瑚的双半萜和西松烷型二萜类化合物。

Biscembranoids and Cembranoids from the Soft Coral Sarcophyton elegans.

作者信息

Li Wei, Zou Yi-Hong, Ge Man-Xi, Lou Lan-Lan, Xu Yun-Shao, Ahmed Abrar, Chen Yun-Yun, Zhang Jun-Sheng, Tang Gui-Hua, Yin Sheng

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.

出版信息

Mar Drugs. 2017 Mar 23;15(4):85. doi: 10.3390/md15040085.

DOI:10.3390/md15040085
PMID:28333090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5408232/
Abstract

Two novel biscembranoids, sarelengans A and B ( and ), five new cembranoids, sarelengans C-G (-), along with two known cembranoids ( and ) were isolated from the South China Sea soft coral . Their structures were determined by spectroscopic and chemical methods, and those of , , , and were confirmed by single crystal X-ray diffraction. Compounds and represent the first example of biscembranoids featuring a -fused A/B-ring conjunction between the two cembranoid units. Their unique structures may shed light on an unusual biosynthetic pathway involving a cembranoid-∆⁸ rather than the normal cembranoid-∆¹ unit in the -Diels-Alder cycloaddition. Compounds and exhibited potential inhibitory effects on nitric oxide production in RAW 264.7 macrophages, with IC values being at 18.2 and 32.5 μM, respectively.

摘要

从中国南海软珊瑚中分离出了两种新型双柏烷类化合物,sarelengans A和B(以及),五种新的柏烷类化合物,sarelengans C-G(-),以及两种已知的柏烷类化合物(和)。通过光谱和化学方法确定了它们的结构,并且通过单晶X射线衍射证实了、、、和的结构。化合物和代表了双柏烷类化合物的首个例子,其在两个柏烷类单元之间具有一个稠合的A/B环连接。它们独特的结构可能为一条不寻常的生物合成途径提供线索,该途径涉及在狄尔斯-阿尔德环加成反应中是柏烷类-Δ⁸而非正常的柏烷类-Δ¹单元。化合物和对RAW 264.7巨噬细胞中一氧化氮的产生表现出潜在的抑制作用,IC值分别为18.2和32.5 μM。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/5e46b9de5c45/marinedrugs-15-00085-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/3a6b9110a4b3/marinedrugs-15-00085-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/1449808bfc77/marinedrugs-15-00085-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/abf29082f853/marinedrugs-15-00085-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/5a1524ace49a/marinedrugs-15-00085-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/909180a368bd/marinedrugs-15-00085-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/94a432eac42c/marinedrugs-15-00085-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/7591af8f8671/marinedrugs-15-00085-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/5e46b9de5c45/marinedrugs-15-00085-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/3a6b9110a4b3/marinedrugs-15-00085-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/1449808bfc77/marinedrugs-15-00085-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/abf29082f853/marinedrugs-15-00085-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/5a1524ace49a/marinedrugs-15-00085-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/909180a368bd/marinedrugs-15-00085-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/94a432eac42c/marinedrugs-15-00085-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/7591af8f8671/marinedrugs-15-00085-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b213/5408232/5e46b9de5c45/marinedrugs-15-00085-g007.jpg

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