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沉香中倍半萜和三萜的抗癌作用。

Anti-Cancer Effect of Sesquiterpene and Triterpenoids from Agarwood of .

机构信息

State Key Lab of Pharmaceutical Biotechnology, College of Life Sciences, Nanjing University, Nanjing 210023, China.

Health Science Center, Institute for Inheritance-Based Innovation of Chinese Medicine, School of Pharmaceutical Sciences, Shenzhen University, Shenzhen 518060, China.

出版信息

Molecules. 2022 Aug 22;27(16):5350. doi: 10.3390/molecules27165350.

DOI:10.3390/molecules27165350
PMID:36014586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9413513/
Abstract

Two new guaiane sesquiterpenes, aquisinenoids A and B ( and ), two new eudesmane-type sesquiterpenoids, aquisinenoids C and D ( and ), one new cucurbitacin, aquisinenoid E (), and five known cucurbitacins (-) were isolated from agarwood of . The structures of these new compounds, including their absolute configurations, were characterized by spectroscopic and computational methods. The biological evaluation showed that compounds and had an anti-cancer effect on most of the cancer cells at 5 μM, especially in human breast cancer cells. Interestingly, the new compound exhibited more sensitivity on cancer cells than normal cells, highlighting its potential as a novel anti-cancer agent. Mechanically, compound treatment increased the ROS generation and triggered apoptosis of human breast cancer cells.

摘要

从沉香属植物中分离得到两个新的愈创木烷型倍半萜,aquisinenoids A 和 B(和),两个新的桉烷型倍半萜,aquisinenoids C 和 D(和),一个新的葫芦素,aquisinenoid E(),和五个已知的葫芦素(-)。这些新化合物的结构,包括它们的绝对构型,是通过光谱和计算方法来确定的。生物评价表明,化合物和在 5 μM 时对大多数癌细胞具有抗癌作用,特别是对人乳腺癌细胞。有趣的是,新化合物在癌细胞中的敏感性高于正常细胞,这突出了它作为一种新型抗癌药物的潜力。在机制上,化合物处理增加了 ROS 的产生并触发了人乳腺癌细胞的凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/71d72ca9a378/molecules-27-05350-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/b909b9a9e276/molecules-27-05350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/13a9583839a6/molecules-27-05350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/64591d8de327/molecules-27-05350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/438be0fac532/molecules-27-05350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/6ec84d1e8740/molecules-27-05350-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/71d72ca9a378/molecules-27-05350-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/b909b9a9e276/molecules-27-05350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/13a9583839a6/molecules-27-05350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/64591d8de327/molecules-27-05350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/438be0fac532/molecules-27-05350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/6ec84d1e8740/molecules-27-05350-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f4/9413513/71d72ca9a378/molecules-27-05350-g006.jpg

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