{"title":"来自六种硅烯的新 C,O-糖基黄酮","authors":"D. N. Olennikov, N. I. Kashchenko","doi":"10.1007/s10600-025-04620-7","DOIUrl":null,"url":null,"abstract":"<p>An investigation of six species of <i>Silene</i> (Caryophyllaceae) cultivated in Baikal District isolated 22 flavonoids, including new <i>C,O</i>-glycosylflavones <b>1–5</b>. The structures of <b>1</b>–<b>5</b> were established using UV and NMR spectroscopy and mass spectrometry as genkwanin 6-<i>C</i>-(2′′-<i>O</i>-<i>β</i>-D-glucopyranosyl)-<i>β</i>-D-glycopyranoside-4′-<i>O</i>-<i>β</i>-D-glucopyranoside (sileneside H, <b>1</b>) and genkwanin 6-<i>C</i>-[2′′-<i>O</i>-(2′′′-<i>O</i>-caffeyl)-<i>β</i>-D-glucopyranosyl]-<i>β</i>-D-glucopyranoside (sileneside I, <b>2</b>) from <i>S. badachschanica</i> Ovcz. and <i>S. daghestanica</i> Rupr.; isovitexin 2′′-<i>O</i>-(2′′′-<i>O</i>-acetyl)-<i>β</i>-D-glucopyranoside-6′′-<i>O</i>-<i>β</i>-D-glucopyranoside (sileneside J, <b>3</b>) from <i>S. dichotoma</i> Ehrh. and <i>S. iberica</i> M. Bieb.; isovitexin 2′′,6′′-di-<i>O</i>-caffeate (sileneside K, <b>4</b>) from <i>S. turgida</i> M. Bieb. ex Bunge; and schaftoside 2′′-<i>O</i>-caffeate (sileneside L, <b>5</b>) from <i>S. sibirica</i> Pers. Compounds <b>2</b> and <b>5</b> possessed antiradical activity.</p>","PeriodicalId":514,"journal":{"name":"Chemistry of Natural Compounds","volume":"61 2","pages":"231 - 236"},"PeriodicalIF":0.8000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"New C,O-Glycosylflavones from Six Species of Silene\",\"authors\":\"D. N. Olennikov, N. I. Kashchenko\",\"doi\":\"10.1007/s10600-025-04620-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>An investigation of six species of <i>Silene</i> (Caryophyllaceae) cultivated in Baikal District isolated 22 flavonoids, including new <i>C,O</i>-glycosylflavones <b>1–5</b>. The structures of <b>1</b>–<b>5</b> were established using UV and NMR spectroscopy and mass spectrometry as genkwanin 6-<i>C</i>-(2′′-<i>O</i>-<i>β</i>-D-glucopyranosyl)-<i>β</i>-D-glycopyranoside-4′-<i>O</i>-<i>β</i>-D-glucopyranoside (sileneside H, <b>1</b>) and genkwanin 6-<i>C</i>-[2′′-<i>O</i>-(2′′′-<i>O</i>-caffeyl)-<i>β</i>-D-glucopyranosyl]-<i>β</i>-D-glucopyranoside (sileneside I, <b>2</b>) from <i>S. badachschanica</i> Ovcz. and <i>S. daghestanica</i> Rupr.; isovitexin 2′′-<i>O</i>-(2′′′-<i>O</i>-acetyl)-<i>β</i>-D-glucopyranoside-6′′-<i>O</i>-<i>β</i>-D-glucopyranoside (sileneside J, <b>3</b>) from <i>S. dichotoma</i> Ehrh. and <i>S. iberica</i> M. Bieb.; isovitexin 2′′,6′′-di-<i>O</i>-caffeate (sileneside K, <b>4</b>) from <i>S. turgida</i> M. Bieb. ex Bunge; and schaftoside 2′′-<i>O</i>-caffeate (sileneside L, <b>5</b>) from <i>S. sibirica</i> Pers. Compounds <b>2</b> and <b>5</b> possessed antiradical activity.</p>\",\"PeriodicalId\":514,\"journal\":{\"name\":\"Chemistry of Natural Compounds\",\"volume\":\"61 2\",\"pages\":\"231 - 236\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-03-25\",\"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/s10600-025-04620-7\",\"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/s10600-025-04620-7","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
摘要
从贝加尔湖地区种植的6种硅烯(石竹科)植物中分离出22种黄酮类化合物,其中包括新的C, o -糖基黄酮1-5。通过紫外、核磁共振、质谱等方法确定了化合物1 ~ 5的结构,分别为荆芥6-C-(2′- o -β- d -葡萄糖苷)-β- d -甘黄苷-4′- o -β- d -葡萄糖苷(沉默苷H, 1)和荆芥6-C-[2′- o -(2′- o -咖啡基)-β- d -葡萄糖苷]-β- d -葡萄糖苷(沉默苷I, 2)。和大菱鲆;异牡荆素2′- o -(2′' - o -乙酰基)-β- d -葡萄糖苷-6′- o -β- d -葡萄糖苷(sileneside J, 3)。伊比利亚螺;异牡荆素2 ',6 ' -二o -咖啡酸酯(沉默苷K, 4)Bunge交货;和schaftoside 2′-O-caffeate (sileneside L, 5)。化合物2和5具有抗自由基活性。
New C,O-Glycosylflavones from Six Species of Silene
An investigation of six species of Silene (Caryophyllaceae) cultivated in Baikal District isolated 22 flavonoids, including new C,O-glycosylflavones 1–5. The structures of 1–5 were established using UV and NMR spectroscopy and mass spectrometry as genkwanin 6-C-(2′′-O-β-D-glucopyranosyl)-β-D-glycopyranoside-4′-O-β-D-glucopyranoside (sileneside H, 1) and genkwanin 6-C-[2′′-O-(2′′′-O-caffeyl)-β-D-glucopyranosyl]-β-D-glucopyranoside (sileneside I, 2) from S. badachschanica Ovcz. and S. daghestanica Rupr.; isovitexin 2′′-O-(2′′′-O-acetyl)-β-D-glucopyranoside-6′′-O-β-D-glucopyranoside (sileneside J, 3) from S. dichotoma Ehrh. and S. iberica M. Bieb.; isovitexin 2′′,6′′-di-O-caffeate (sileneside K, 4) from S. turgida M. Bieb. ex Bunge; and schaftoside 2′′-O-caffeate (sileneside L, 5) from S. sibirica Pers. Compounds 2 and 5 possessed antiradical activity.
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.