Junzhi Pan , Huayuan Liu , Junpeng Xu , Xiaofeng Xu , Yu Qi , Chaojie Wang , Changle Wu , Zhongmin Sun , Yali Lv , Pengcheng Yan
{"title":"中国海褐藻马尾藻中的五种新的色烷经二萜类化合物","authors":"Junzhi Pan , Huayuan Liu , Junpeng Xu , Xiaofeng Xu , Yu Qi , Chaojie Wang , Changle Wu , Zhongmin Sun , Yali Lv , Pengcheng Yan","doi":"10.1016/j.phytol.2024.11.001","DOIUrl":null,"url":null,"abstract":"<div><div>Five previously undescribed chromane-type meroditerpenoids, sargasilols J–N (<strong>1</strong>–<strong>5</strong>), were isolated from an EtOAc-soluble extract of the brown alga <em>Sargassum siliquastrum</em> collected in the China Sea. The chemical structures of these meroditerpenoids were determined by extensive spectroscopic analyses, including 1D/2D NMR, ECD, and HR-ESI-MS data. Compound <strong>3</strong> exhibited potent anti-neuroinflammatory activity against lipopolysaccharide (LPS)-induced nitric oxide (NO) production in BV-2 microglia cells, with an IC<sub>50</sub> value of 9.9 <em>μ</em>M.</div></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"64 ","pages":"Pages 133-137"},"PeriodicalIF":1.3000,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Five new chromane meroditerpenoids from the brown alga Sargassum siliquastrum of China Sea\",\"authors\":\"Junzhi Pan , Huayuan Liu , Junpeng Xu , Xiaofeng Xu , Yu Qi , Chaojie Wang , Changle Wu , Zhongmin Sun , Yali Lv , Pengcheng Yan\",\"doi\":\"10.1016/j.phytol.2024.11.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Five previously undescribed chromane-type meroditerpenoids, sargasilols J–N (<strong>1</strong>–<strong>5</strong>), were isolated from an EtOAc-soluble extract of the brown alga <em>Sargassum siliquastrum</em> collected in the China Sea. The chemical structures of these meroditerpenoids were determined by extensive spectroscopic analyses, including 1D/2D NMR, ECD, and HR-ESI-MS data. Compound <strong>3</strong> exhibited potent anti-neuroinflammatory activity against lipopolysaccharide (LPS)-induced nitric oxide (NO) production in BV-2 microglia cells, with an IC<sub>50</sub> value of 9.9 <em>μ</em>M.</div></div>\",\"PeriodicalId\":20408,\"journal\":{\"name\":\"Phytochemistry Letters\",\"volume\":\"64 \",\"pages\":\"Pages 133-137\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2024-11-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytochemistry Letters\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1874390024001484\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytochemistry Letters","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1874390024001484","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Five new chromane meroditerpenoids from the brown alga Sargassum siliquastrum of China Sea
Five previously undescribed chromane-type meroditerpenoids, sargasilols J–N (1–5), were isolated from an EtOAc-soluble extract of the brown alga Sargassum siliquastrum collected in the China Sea. The chemical structures of these meroditerpenoids were determined by extensive spectroscopic analyses, including 1D/2D NMR, ECD, and HR-ESI-MS data. Compound 3 exhibited potent anti-neuroinflammatory activity against lipopolysaccharide (LPS)-induced nitric oxide (NO) production in BV-2 microglia cells, with an IC50 value of 9.9 μM.
期刊介绍:
Phytochemistry Letters invites rapid communications on all aspects of natural product research including:
• Structural elucidation of natural products
• Analytical evaluation of herbal medicines
• Clinical efficacy, safety and pharmacovigilance of herbal medicines
• Natural product biosynthesis
• Natural product synthesis and chemical modification
• Natural product metabolism
• Chemical ecology
• Biotechnology
• Bioassay-guided isolation
• Pharmacognosy
• Pharmacology of natural products
• Metabolomics
• Ethnobotany and traditional usage
• Genetics of natural products
Manuscripts that detail the isolation of just one new compound are not substantial enough to be sent out of review and are out of scope. Furthermore, where pharmacology has been performed on one new compound to increase the amount of novel data, the pharmacology must be substantial and/or related to the medicinal use of the producing organism.