Xue-Xue Cheng , Ya-Feng Wang , Rui-Jie He , Bing-Yuan Yang , Zhang-Bin Liu , Yong-Lin Huang
{"title":"从栲叶中提取的三种新的喹酸衍生物和一种新的莽草酸衍生物","authors":"Xue-Xue Cheng , Ya-Feng Wang , Rui-Jie He , Bing-Yuan Yang , Zhang-Bin Liu , Yong-Lin Huang","doi":"10.1016/j.phytol.2024.04.014","DOIUrl":null,"url":null,"abstract":"<div><p>Three new quinic acids derivatives, 3-<em>O</em>-<em>trans-</em>caffeoyl-5-<em>O</em>-galloylquinic acid (<strong>1</strong>), 3-<em>O</em>-<em>trans</em>-caffeoly-5-<em>O</em>-galloylquinic acid methyl ester (<strong>2</strong>), 3-<em>O</em>-<em>trans</em>-caffeoyl-4-<em>O</em>-galloylquinic acid methyl ester (<strong>3</strong>), and a new shikimic acid derivative as orthacanthain A (<strong>4</strong>), along with three known compounds, 3-<em>O</em>-caffeoylquinic acid (<strong>5</strong>), methyl-3-<em>O</em>-galloylquinic acid (<strong>6</strong>), and emblifatmin (<strong>7</strong>), were isolated from the 70% methanol extract of the leaves of <em>Castanopsis orthacantha</em> France. The structures of all compounds were identified by optical rotation, MS, UV, IR, 1D and 2D NMR spectral data and comparison with literature. The IC<sub>50</sub> value of compound <strong>3</strong> was (0.024±0.009) mmol/L, which had strong inhibitory activity on α-glucosidase.</p></div>","PeriodicalId":20408,"journal":{"name":"Phytochemistry Letters","volume":"61 ","pages":"Pages 182-186"},"PeriodicalIF":1.3000,"publicationDate":"2024-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Three new quinic acid derivatives and a new shikimic acid derivative from the leaves of Castanopsis orthacantha\",\"authors\":\"Xue-Xue Cheng , Ya-Feng Wang , Rui-Jie He , Bing-Yuan Yang , Zhang-Bin Liu , Yong-Lin Huang\",\"doi\":\"10.1016/j.phytol.2024.04.014\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Three new quinic acids derivatives, 3-<em>O</em>-<em>trans-</em>caffeoyl-5-<em>O</em>-galloylquinic acid (<strong>1</strong>), 3-<em>O</em>-<em>trans</em>-caffeoly-5-<em>O</em>-galloylquinic acid methyl ester (<strong>2</strong>), 3-<em>O</em>-<em>trans</em>-caffeoyl-4-<em>O</em>-galloylquinic acid methyl ester (<strong>3</strong>), and a new shikimic acid derivative as orthacanthain A (<strong>4</strong>), along with three known compounds, 3-<em>O</em>-caffeoylquinic acid (<strong>5</strong>), methyl-3-<em>O</em>-galloylquinic acid (<strong>6</strong>), and emblifatmin (<strong>7</strong>), were isolated from the 70% methanol extract of the leaves of <em>Castanopsis orthacantha</em> France. The structures of all compounds were identified by optical rotation, MS, UV, IR, 1D and 2D NMR spectral data and comparison with literature. The IC<sub>50</sub> value of compound <strong>3</strong> was (0.024±0.009) mmol/L, which had strong inhibitory activity on α-glucosidase.</p></div>\",\"PeriodicalId\":20408,\"journal\":{\"name\":\"Phytochemistry Letters\",\"volume\":\"61 \",\"pages\":\"Pages 182-186\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2024-05-07\",\"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/S1874390024000703\",\"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/S1874390024000703","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 quinic acid derivatives and a new shikimic acid derivative from the leaves of Castanopsis orthacantha
Three new quinic acids derivatives, 3-O-trans-caffeoyl-5-O-galloylquinic acid (1), 3-O-trans-caffeoly-5-O-galloylquinic acid methyl ester (2), 3-O-trans-caffeoyl-4-O-galloylquinic acid methyl ester (3), and a new shikimic acid derivative as orthacanthain A (4), along with three known compounds, 3-O-caffeoylquinic acid (5), methyl-3-O-galloylquinic acid (6), and emblifatmin (7), were isolated from the 70% methanol extract of the leaves of Castanopsis orthacantha France. The structures of all compounds were identified by optical rotation, MS, UV, IR, 1D and 2D NMR spectral data and comparison with literature. The IC50 value of compound 3 was (0.024±0.009) mmol/L, which had strong inhibitory activity on α-glucosidase.
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.