{"title":"沙棘果实中具有保肝活性的结构多样性黄酮木脂素","authors":"Qinge Ma, Wenmin Liu, Rongrui Wei","doi":"10.1007/s10600-025-04729-9","DOIUrl":null,"url":null,"abstract":"<p>A novel flavonolignan, named 3,3′,4′,5-tetrahydroxy-3′′′,5′′′-dimethoxy-9′,9′′′dihydroxymethyl-4- hydroxyphenyl-4′′′-hydroxy-3′′′,5′′′-dimethoxyphenylflavonolignan (<b>1</b>), together with five known flavonolignan derivatives (<b>2–6</b>) were isolated from <i>Hippophae rhamnoides</i> L. for the first time. Their structures were determined by extensive and comprehensive IR, UV, NMR, MS spectra, as well as reported references. Compounds <b>1–6</b> were evaluated for their hepatoprotective activities on APAP-treated HepG2 cells. As a result, compounds <b>1</b> and <b>2</b> exhibited moderate hepatoprotective activities.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 4","pages":"648 - 652"},"PeriodicalIF":0.9000,"publicationDate":"2025-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structurally Diverse Flavonolignans with Hepatoprotective Activities from the Fruits of Hippophae rhamnoides\",\"authors\":\"Qinge Ma, Wenmin Liu, Rongrui Wei\",\"doi\":\"10.1007/s10600-025-04729-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A novel flavonolignan, named 3,3′,4′,5-tetrahydroxy-3′′′,5′′′-dimethoxy-9′,9′′′dihydroxymethyl-4- hydroxyphenyl-4′′′-hydroxy-3′′′,5′′′-dimethoxyphenylflavonolignan (<b>1</b>), together with five known flavonolignan derivatives (<b>2–6</b>) were isolated from <i>Hippophae rhamnoides</i> L. for the first time. Their structures were determined by extensive and comprehensive IR, UV, NMR, MS spectra, as well as reported references. Compounds <b>1–6</b> were evaluated for their hepatoprotective activities on APAP-treated HepG2 cells. As a result, compounds <b>1</b> and <b>2</b> exhibited moderate hepatoprotective activities.</p>\",\"PeriodicalId\":514,\"journal\":{\"name\":\"Chemistry of Natural Compounds\",\"volume\":\"61 4\",\"pages\":\"648 - 652\"},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2025-07-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry of Natural Compounds\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10600-025-04729-9\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry of Natural Compounds","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10600-025-04729-9","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Structurally Diverse Flavonolignans with Hepatoprotective Activities from the Fruits of Hippophae rhamnoides
A novel flavonolignan, named 3,3′,4′,5-tetrahydroxy-3′′′,5′′′-dimethoxy-9′,9′′′dihydroxymethyl-4- hydroxyphenyl-4′′′-hydroxy-3′′′,5′′′-dimethoxyphenylflavonolignan (1), together with five known flavonolignan derivatives (2–6) were isolated from Hippophae rhamnoides L. for the first time. Their structures were determined by extensive and comprehensive IR, UV, NMR, MS spectra, as well as reported references. Compounds 1–6 were evaluated for their hepatoprotective activities on APAP-treated HepG2 cells. As a result, compounds 1 and 2 exhibited moderate hepatoprotective activities.
期刊介绍:
Chemistry of Natural Compounds publishes reviews and general articles about the structure of different classes of natural compounds, the chemical characteristics of botanical families, genus, and species, to establish the comparative laws and connection between physiological activity and the structure of substances.