Article(id=1304406849072165792, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.01.002, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1762444800000, receivedDateStr=2025-11-07, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788924427525, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788924427525, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788924427525, creator=13701087609, updateTime=1788924427525, updator=13701087609, issue=Issue{id=1304406818550206926, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='1', pageStart='1', pageEnd='389', issueExtLink='null', onlineDate='null', pubDate='1768147200000', pubDateStr='2026-01-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788924420249, creator='13701087609', updateTime=1788924674802, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304407886289986387, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304407886289986388, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406818550206926, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=13, endPage=23, ext={EN=ArticleExt(id=1304406849403515810, articleId=1304406849072165792, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=A new oleanane-type triterpenoid glycoside from n-butanol fraction of Primulina eburnea from Guizhou, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To study the chemical constituents, antioxidant activity and anti-inflammatory activity of the n-butanol fraction from Primulina eburnea. Methods Compounds were separated and purified using chromatographic techniques such as normal-phase and reversed-phase silica gel column chromatography, Sephadex LH-20 gel column chromatography and RP-HPLC. Meanwhile, their structures were identified by spectroscopic techniques including NMR, UV and IR. Subsequently, the antioxidant activities of obtained compounds were evaluated by the DPPH and ABTS assays, while the Griess assay was employed to determine the effect of these compounds on NO production in lipopolysaccharide (LPS)-induced RAW264.7 cells to assess their anti-inflammatory activity. Results A total of 20 compounds were isolated from the n-butanol fraction of P. eburnea and were respectively identified as spathodic acid-28-O-β-D-gentiobioside (1), calceolarioside B (2), 2-(3,4-dihydroxyphenyl)ethanol glucoside (3), salidroside (4), tyrosol (5), 6-hydroxyapigenin-7-O-β-[2-O-β-xyloglucoside] (6), icariol A₂(7), (+)-isolariciresinol (8), 5-methoxy-(+)-isolariciresinol (9), (+)-syringaresinol-4'-O-β-D-glucopyranoside (10), dihydrophaseic acid (11), (6S,9R)-roseoside (12), esculetin (13), p-hydroxybenzoic acid (14), protocatechuic acid (15), vanillic acid (16), syringic acid (17), caffeic acid (18), caffeic acid methyl ester (19) and methyl-3-O-β-D-glucopyranosyl-4-hydroxy caffeic acid (20). Meanwhile, compounds 7, 17 and 18 exhibited significant antioxidant activity. Compounds 3, 5—9 exhibited significant inhibitory effects on the production of NO in LPS-induced RAW264.7 cells. Conclusion Compound 1 is a new triterpenoid glycoside, named eburneoside A. While compounds 4, 6, 9—12, 14, 15 and 20 were isolated for the first time from the genus Primulina. Additionally, compounds 17 and 18 were firstly isolated from P. eburnea. Furthermore, some of these compounds exhibited significant antioxidant and anti-inflammatory activities., authors=HUANG Hongying, CHEN Junlei, LIU Siyan, CHEN Quan, CHEN Xingxin, CHEN Xianrong, HAO Xiaojiang, GU Wei, authorsList=HUANG Hongying, CHEN Junlei, LIU Siyan, CHEN Quan, CHEN Xingxin, CHEN Xianrong, HAO Xiaojiang, GU Wei, authorCompany=null, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1304406849311241121, articleId=1304406849072165792, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=黔产牛耳朵正丁醇部位中1个新的齐墩果烷型三萜糖苷, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究牛耳朵Primulina eburnea正丁醇部位的化学成分及其抗氧化和抗炎活性。方法 运用正、反相硅胶柱色谱、Sephadex LH-20凝胶柱色谱与RP-HPLC等色谱学技术对化合物进行分离纯化，并结合NMR、UV、IR等光谱学技术对其结构进行鉴定。进一步利用1,1-二苯基-2-三硝基苯肼自由基（1,1-diphenyl-2-picrylhydrazyl，DPPH）法和总抗氧化能力检测试剂盒 [total antioxidant capacity (T-AOC) assay kit，ABTS] 法评价所得化合物的抗氧化活性，采用Griess法检测化合物对脂多糖（lipopolysaccharide，LPS）诱导RAW264.7细胞产生NO的影响来评估其抗炎活性。结果 从牛耳朵正丁醇部位中分离得到20个化合物，分别鉴定为火焰木酸-28-O-β-D-龙胆二糖苷（1）、木通苯乙醇苷B（2）、2-(3,4-二羟基苯基)乙醇葡萄糖苷（3）、红景天苷（4）、酪醇（5）、6-hydroxyapigenin-7-O-β-[2-O-β-xyloglucoside]（6）、淫羊藿醇A₂（7）、(＋)-异落叶松脂素（8）、5-甲氧基-(＋)-异落叶松脂素（9）、(＋)-丁香脂素-4¢-O-β-D-吡喃葡萄糖苷（10）、二氢菜豆酸（11）、(6S,9R)-长寿花糖苷（12）、七叶内酯（13）、对羟基苯甲酸（14）、原儿茶酸（15）、香草酸（16）、丁香酸（17）、咖啡酸（18）、咖啡酸甲酯（19）、3-O-β-D-吡喃葡萄糖基-4-羟基咖啡酸甲酯（20）。化合物7、17和18表现出显著的抗氧化活性。化合物3、5～9对LPS诱导的RAW264.7细胞中NO的生成有显著的抑制作用。结论 化合物1为新的三萜糖苷类，命名为牛耳朵苷A，化合物4、6、7、9～12、14、15和20为报春苣苔属植物首次分得，化合物17和18为牛耳朵植物中首次分得，且部分化合物表现出显著抗氧化和抗炎活性。, authors=黄红英¹, 陈俊磊¹, 刘思妍¹, 陈泉¹, 陈兴欣¹, 陈显容¹, 郝小江¹, 顾玮¹, authorsList=黄红英, 陈俊磊, 刘思妍, 陈泉, 陈兴欣, 陈显容, 郝小江, 顾玮, authorCompany=1 中药功效成分发掘与利用全国重点实验室, 贵州医科大学药学院, 贵州省天然产物研究中心, 贵州 贵阳 550014, correspAuthors=郝小江, authorNote=黄红英: 黄红英,硕士研究生,研究方向为天然药物化学。E-mail:2836168052@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=HkaGDCRfp7Xuk2HggO4Hwg==, pdfFileSize=1689525, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=贵州省自然科学基金重点项目 (黔科合基础-ZK[2024]重点084))}, authors=[Author(id=1307432723463827746, tenantId=1146029695717560320, journalId=null, articleId=1304406849072165792, orderNo=null, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=null, email=null, emailSecond=null, emailThird=null, 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