Sappanumols A–C, Three Homoisoflavonoids with Antiinflammatory Activities from Sappan lignum

IF 5 1区 化学 Q1 CHEMISTRY, ORGANIC
Qi-Qi Wang, Hao-Jie Liu, Guo-Qing Qin, Chen Hong, Jun Lin, Ping Yang, Yue Shen, Ke-Wu Zeng, Qing-Ying Zhang* and Peng-Fei Tu*, 
{"title":"Sappanumols A–C, Three Homoisoflavonoids with Antiinflammatory Activities from Sappan lignum","authors":"Qi-Qi Wang,&nbsp;Hao-Jie Liu,&nbsp;Guo-Qing Qin,&nbsp;Chen Hong,&nbsp;Jun Lin,&nbsp;Ping Yang,&nbsp;Yue Shen,&nbsp;Ke-Wu Zeng,&nbsp;Qing-Ying Zhang* and Peng-Fei Tu*,&nbsp;","doi":"10.1021/acs.orglett.5c02020","DOIUrl":null,"url":null,"abstract":"<p >Sappanumols A–C (<b>1</b>–<b>3</b>, respectively), three unprecedented homoisoflavonoids, were isolated from <i>Sappan lignum</i>. Their structures were elucidated by comprehensive spectroscopic analysis and ECD computation methods. Compound <b>3</b> demonstrated inhibitory effects on LPS-induced NO production in BV-2 cells with an IC<sub>50</sub> value of 16.99 <i>μ</i>M. Compound <b>3</b> decreased the levels of TNF-α and IL-6 in a dose-dependent manner and exhibited significant anti-inflammatory activity in a zebrafish inflammation model.</p>","PeriodicalId":54,"journal":{"name":"Organic Letters","volume":"27 29","pages":"7822–7826"},"PeriodicalIF":5.0000,"publicationDate":"2025-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Letters","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.orglett.5c02020","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

Sappanumols A–C (13, respectively), three unprecedented homoisoflavonoids, were isolated from Sappan lignum. Their structures were elucidated by comprehensive spectroscopic analysis and ECD computation methods. Compound 3 demonstrated inhibitory effects on LPS-induced NO production in BV-2 cells with an IC50 value of 16.99 μM. Compound 3 decreased the levels of TNF-α and IL-6 in a dose-dependent manner and exhibited significant anti-inflammatory activity in a zebrafish inflammation model.

Abstract Image

三种具有抗炎活性的参木同型异黄酮。
从皂荚木中分离到三种同源异黄酮,分别为A-C(1-3)。通过综合光谱分析和ECD计算方法对其结构进行了分析。化合物3对lps诱导的BV-2细胞NO生成有抑制作用,IC50值为16.99 μM。化合物3在斑马鱼炎症模型中呈剂量依赖性降低TNF-α和IL-6水平,并表现出显著的抗炎活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Organic Letters
Organic Letters 化学-有机化学
CiteScore
9.30
自引率
11.50%
发文量
1607
审稿时长
1.5 months
期刊介绍: Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.
×
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:604180095
Book学术官方微信