{"title":"从盐肤木叶中提取的三种新的酚苷","authors":"Xin Chen , Zhengxiang Tong , Rongtao Li , Jianguo Zeng","doi":"10.1016/j.phytol.2024.05.002","DOIUrl":null,"url":null,"abstract":"<div><p>Three new phenolic glycosides, including 3-hydroxy-5-methylphenol 1-<em>O</em>-<em>β</em>-D-(6′-<em>O</em>-cinnamoyl)-glucopyranoside (<strong>1</strong>), 3-hydroxy-5-methylphenol 1-<em>O</em>-<em>β</em>-D-(6′-<em>O</em>-<em>p</em>-hydroxycinnamoyl)-glucopyranoside (<strong>2</strong>), 3-hydroxy-5-methylphenol 1-<em>O</em>-<em>β</em>-D-(6′-<em>O</em>-<em>p</em>-hydroxybenzoyl)-glucopyranoside (<strong>3</strong>), were isolated from the leaves of <em>Rhus chinensis</em> Mill, together with seven known compounds (<strong>4-10</strong>). Their structures were elucidated on the basis of extensive NMR spectral and high resolution mass spectrometry analysis. Among the isolated compounds, butein (4), quercetin (5), and ethyl gallate (6) exhibited moderate NO production in RAW264.7 cells induced by LPS with IC<sub>50</sub> values of 21.29 ± 0.54, 34.26 ± 2.09 and 42.59 ± 0.11 <em>μ</em>M, compared with postive control L-NMMA (a nitric oxide synthase inhibitor, IC<sub>50</sub> 38.41 ± 0.32 <em>μ</em>M).</p></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"61 ","pages":"Pages 222-225"},"PeriodicalIF":1.3000,"publicationDate":"2024-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Three new phenolic glycosides from Rhus chinensis leaves\",\"authors\":\"Xin Chen , Zhengxiang Tong , Rongtao Li , Jianguo Zeng\",\"doi\":\"10.1016/j.phytol.2024.05.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Three new phenolic glycosides, including 3-hydroxy-5-methylphenol 1-<em>O</em>-<em>β</em>-D-(6′-<em>O</em>-cinnamoyl)-glucopyranoside (<strong>1</strong>), 3-hydroxy-5-methylphenol 1-<em>O</em>-<em>β</em>-D-(6′-<em>O</em>-<em>p</em>-hydroxycinnamoyl)-glucopyranoside (<strong>2</strong>), 3-hydroxy-5-methylphenol 1-<em>O</em>-<em>β</em>-D-(6′-<em>O</em>-<em>p</em>-hydroxybenzoyl)-glucopyranoside (<strong>3</strong>), were isolated from the leaves of <em>Rhus chinensis</em> Mill, together with seven known compounds (<strong>4-10</strong>). Their structures were elucidated on the basis of extensive NMR spectral and high resolution mass spectrometry analysis. Among the isolated compounds, butein (4), quercetin (5), and ethyl gallate (6) exhibited moderate NO production in RAW264.7 cells induced by LPS with IC<sub>50</sub> values of 21.29 ± 0.54, 34.26 ± 2.09 and 42.59 ± 0.11 <em>μ</em>M, compared with postive control L-NMMA (a nitric oxide synthase inhibitor, IC<sub>50</sub> 38.41 ± 0.32 <em>μ</em>M).</p></div>\",\"PeriodicalId\":20408,\"journal\":{\"name\":\"Phytochemistry Letters\",\"volume\":\"61 \",\"pages\":\"Pages 222-225\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2024-05-21\",\"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/S1874390024000740\",\"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/S1874390024000740","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Three new phenolic glycosides from Rhus chinensis leaves
Three new phenolic glycosides, including 3-hydroxy-5-methylphenol 1-O-β-D-(6′-O-cinnamoyl)-glucopyranoside (1), 3-hydroxy-5-methylphenol 1-O-β-D-(6′-O-p-hydroxycinnamoyl)-glucopyranoside (2), 3-hydroxy-5-methylphenol 1-O-β-D-(6′-O-p-hydroxybenzoyl)-glucopyranoside (3), were isolated from the leaves of Rhus chinensis Mill, together with seven known compounds (4-10). Their structures were elucidated on the basis of extensive NMR spectral and high resolution mass spectrometry analysis. Among the isolated compounds, butein (4), quercetin (5), and ethyl gallate (6) exhibited moderate NO production in RAW264.7 cells induced by LPS with IC50 values of 21.29 ± 0.54, 34.26 ± 2.09 and 42.59 ± 0.11 μM, compared with postive control L-NMMA (a nitric oxide synthase inhibitor, IC50 38.41 ± 0.32 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.