灵芝中的 3,4-seco-三萜类抗炎物质

IF 2.1 3区 化学 Q2 CHEMISTRY, ORGANIC
{"title":"灵芝中的 3,4-seco-三萜类抗炎物质","authors":"","doi":"10.1016/j.tet.2024.134240","DOIUrl":null,"url":null,"abstract":"<div><p>Five new 3,4-<em>seco</em>-lanostane triterpenoids, named ganocochnoids A−E (1−5), along with three known analogues (6−8), were isolated from <em>Ganoderma cochlear</em>. The structures of these new compounds, including their absolute configurations, were characterized by 1D and 2D nuclear magnetic resonance (NMR), computational methods, and HRESIMS. In particular, the structure of compound 1 was confirmed through X-ray crystallographic analysis. The anti-inflammatory activity of all the compounds was evaluated in LPS-induced RAW264.7 cells. The Western blot assay indicated that compounds <strong>4</strong> and <strong>5</strong> were found to have inhibitory effects on iNOS protein expression as well as on mRNA levels of <em>TNF-a</em>, <em>Il-1b</em>, and <em>Il-6</em>, and compound <strong>4</strong> also reduced COX-2 protein expression in LPS-induced RAW264.7 cells.</p></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anti-inflammatory 3,4-seco-triterpenoids from Ganoderma cochlear\",\"authors\":\"\",\"doi\":\"10.1016/j.tet.2024.134240\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Five new 3,4-<em>seco</em>-lanostane triterpenoids, named ganocochnoids A−E (1−5), along with three known analogues (6−8), were isolated from <em>Ganoderma cochlear</em>. The structures of these new compounds, including their absolute configurations, were characterized by 1D and 2D nuclear magnetic resonance (NMR), computational methods, and HRESIMS. In particular, the structure of compound 1 was confirmed through X-ray crystallographic analysis. The anti-inflammatory activity of all the compounds was evaluated in LPS-induced RAW264.7 cells. The Western blot assay indicated that compounds <strong>4</strong> and <strong>5</strong> were found to have inhibitory effects on iNOS protein expression as well as on mRNA levels of <em>TNF-a</em>, <em>Il-1b</em>, and <em>Il-6</em>, and compound <strong>4</strong> also reduced COX-2 protein expression in LPS-induced RAW264.7 cells.</p></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-09-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040402024004204\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040402024004204","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

研究人员从灵芝中分离出了五种新的 3,4-seco-lanostane三萜类化合物,命名为灵芝素 A-E(1-5),以及三种已知的类似物(6-8)。通过一维和二维核磁共振(NMR)、计算方法和 HRESIMS 对这些新化合物的结构(包括其绝对构型)进行了表征。其中,化合物 1 的结构通过 X 射线晶体学分析得到了证实。在 LPS 诱导的 RAW264.7 细胞中评估了所有化合物的抗炎活性。Western 印迹分析表明,化合物 4 和 5 对 LPS 诱导的 RAW264.7 细胞中 iNOS 蛋白表达以及 TNF-a、Il-1b 和 Il-6 的 mRNA 水平有抑制作用,化合物 4 还能降低 COX-2 蛋白表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anti-inflammatory 3,4-seco-triterpenoids from Ganoderma cochlear

Anti-inflammatory 3,4-seco-triterpenoids from Ganoderma cochlear

Five new 3,4-seco-lanostane triterpenoids, named ganocochnoids A−E (1−5), along with three known analogues (6−8), were isolated from Ganoderma cochlear. The structures of these new compounds, including their absolute configurations, were characterized by 1D and 2D nuclear magnetic resonance (NMR), computational methods, and HRESIMS. In particular, the structure of compound 1 was confirmed through X-ray crystallographic analysis. The anti-inflammatory activity of all the compounds was evaluated in LPS-induced RAW264.7 cells. The Western blot assay indicated that compounds 4 and 5 were found to have inhibitory effects on iNOS protein expression as well as on mRNA levels of TNF-a, Il-1b, and Il-6, and compound 4 also reduced COX-2 protein expression in LPS-induced RAW264.7 cells.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Tetrahedron
Tetrahedron 化学-有机化学
CiteScore
3.90
自引率
4.80%
发文量
439
审稿时长
34 days
期刊介绍: Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry. Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters. Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信