Article(id=1304415534515249702, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304415531491152712, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.09.002, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1769097600000, receivedDateStr=2026-01-23, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788926498296, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788926498296, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788926498296, creator=13701087609, updateTime=1788926498296, updator=13701087609, issue=Issue{id=1304415531491152712, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='9', pageStart='3261', pageEnd='3684', issueExtLink='null', onlineDate='null', pubDate='1778515200000', pubDateStr='2026-05-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788926497576, creator='13701087609', updateTime=1788926796984, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304416787358049066, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304415531491152712, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304416787358049067, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304415531491152712, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=3274, endPage=3280, ext={EN=ArticleExt(id=1304415536226525736, articleId=1304415534515249702, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Chemical constituents of Tibetan medicine Ligularia virgaurea, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical constituents of Tibetan medicine Ligularia virgaurea. Methods The compounds were isolated and purified by silica gel column chromatography, Sephadex LH-20, ODS reversed-phase column chromatography and semi-preparative HPLC, and the structures were identified by spectral data (NMR and MS). Results A total of 19 compounds were isolated and identified as follows 1-[(1S,3aR,4R,7S,7aS)-4-hydroxy-4-hydroxymethyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone (1), 10α-hydroxy-1-oxoeremophila-7(11),8(9)-dien-12,8-olide (2), 6α,10α-dihydroxy-1-oxoeremophila-7(11),8(9)-dien-12,8-olide (3), 3-hydroxycacalolide (4), 6β-acetoxy-9-oxo-10αH-furanoeremophilane (5), pinoresinol (6), medioresinol (7), syringaresinol (8), p-hydroxybenzoic acid (9), methyl 3,4-dihydroxybenzoate (10), syringic acid (11), 3,4,5-trimethoxybenzoic acid (12), dimethy phthalate (13), syringin (14)、lupeol (15), obtusifoliol (16), ethyl linoleate (17), 15-vaccenic acid (18), 10-eicosenoic acid (19). Conclusion Compound 1 is a new compound, designated 14-hydroxy-oplopanone. Compounds 514, 1619 are isolated from L. virgaurea for the first time., authors=WANG Yao, ZHANG Xinyu, LIAO Jiahui, WANG Hongling, authorsList=WANG Yao, ZHANG Xinyu, LIAO Jiahui, WANG Hongling, 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=1304415536125862439, articleId=1304415534515249702, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=藏药黄帚橐吾化学成分研究, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究藏药黄帚橐吾Ligularia virgaurea的化学成分。方法 采用硅胶柱色谱、Sephadex LH-20、ODS反相柱色谱与半制备HPLC对黄帚橐吾进行分离纯化,结合NMR、MS等波谱学方法鉴定化合物结构。结果 从黄帚橐吾石油醚和醋酸乙酯部位中分离得到19个化合物,分别鉴定为1-[(1S,3aR,4R,7S,7aS)-4-羟基-4-羟甲基-7-异丙基-1,2,3,3a,5,6,7,7a-八氢茚-1-基]乙酮(1)、10α-hydroxy-1-oxoeremophila-7(11),8(9)-dien-12,8-olide(2)、6α,10α-dihydroxy-1-oxoeremophila-7(11),8(9)-dien-12,8-olide(3)、3-hydroxycacalolide(4)、6β-acetoxy-9-oxo-10αH-furanoeremophilane(5)、松脂醇(6)、皮树脂醇(7)、丁香脂素(8)、对羟基苯甲酸(9)、3,4-二羟基苯甲酸甲酯(10)、丁香酸(syringic acid,11)、3,4,5-三甲氧基苯甲酸(3,4,5-trimethoxybenzoic acid,12)、邻苯二甲酸二甲酯(13)、紫丁香苷(14)、羽扇豆醇(15)、钝叶醇(16)、亚油酸乙酯(17)、15-十八碳烯酸(18)、10-二十碳烯酸(19)。结论 其中,化合物1为新化合物,命名为黄帚橐吾酮A(14-hydroxy-oplopanone);化合物5141619均为首次从黄帚橐吾中分离得到。, authors=王瑶1, 张馨予1, 廖佳慧1, 王洪玲1, authorsList=王瑶, 张馨予, 廖佳慧, 王洪玲, authorCompany=1 江西中医药大学, 中药资源与民族药研究中心, 江西 南昌 330004, correspAuthors=王洪玲, authorNote=王瑶: 王瑶(2002-),女,汉族,硕士研究生,主要从事中药尤其是民族药药效物质基础研究。E-mail:wangyao1@jxutcm.edu.cn, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=Qbw8Wy+TayOz9ttvU8tGuQ==, pdfFileSize=1023090, 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=国家自然科学基金资助项目(U2202213);国家自然科学基金资助项目(32470428))}, authors=null, keywords=[Keyword(id=1304415536394297897, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304415534515249702, language=CN, orderNo=1, keyword=藏药), Keyword(id=1304415536482378282, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304415534515249702, language=CN, orderNo=2, keyword=黄帚橐吾), Keyword(id=1304415536562070059, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304415534515249702, language=CN, orderNo=3, keyword=黄帚橐吾酮A), Keyword(id=1304415536616596012, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304415534515249702, language=CN, orderNo=4, keyword=松脂醇), Keyword(id=1304415536687899181, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304415534515249702, language=CN, orderNo=5, keyword=皮树脂醇), Keyword(id=1304415536792756782, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304415534515249702, language=CN, orderNo=6, keyword=紫丁香苷), Keyword(id=1304415536868254255, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304415534515249702, language=CN, orderNo=7, keyword=15-十八碳烯酸), Keyword(id=1304415536960528944, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304415534515249702, language=EN, orderNo=1, keyword=Tibetan medicine), Keyword(id=1304415537027637809, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304415534515249702, language=EN, orderNo=2, keyword=Ligularia virgaurea (Maxim.) 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Marcelo D, Olov S, Nelson H. Furanoeremophilanes from Senecio clivicolus Weddell[J]. Bolivian J Chem, 2013,30(1):80-83.
In S J, Seo K H, Song N Y, et al. Lignans and neolignans from the stems of Vibrunum erosum and their neuroprotective and anti-inflammatory activity[J]. Arch Pharmacal Res, 2015, 38(1):26-34.
王威,刘小红,高华,等.东北铁线莲地上部位化学成分研究[J].中草药, 2014, 45(17):2440-2446
邓雪红,郑承剑,吴宇,等.爬岩红化学成分研究[J].中国药学杂志, 2013, 48(10):777-781.
柳建军,刘锡葵.黄连木食用部位化学成分研究[J].中草药, 2009, 40(2):186-189.
Luo X D, Wu S H, Ma Y B, et al. Chemical constituents from Dysoxylum hainanense[J]. Acta Bot Yunnan, 2001,3:368-372.
乔灏祎,叶贤胜,赫军,等.山茱萸中一个新的环烯醚萜苷类化合物[J].中国药学杂志, 2017, 52(14):1212-1216.
吴培云,蔡百祥,王国凯,等.紫藤瘤化学成分研究(II)[J].中药材, 2017, 40(2):338-341.
秦淳,林秀萍,艾文,等.红树林植物无瓣海桑内生真菌Neofusicoccum sp. SaBA3次级代谢产物的研究[J].天然产物研究与开发, 2014, 26(8):1212-1215.
Ahmad G, Soodabeh S, Matin B M, et al. Phytochemical and chemotaxonomic investigation of Stelleropsis iranica[J]. Aust J Basic Appl Sci, 2009, 3(4):3423-3427.
Fotie J, Bohle D S, Leimanis M L, et al. Lupeol long-chain fatty acid esters with antimalarial activity from Holarrhena floribunda[J]. J Nat Prod, 2006, 69(1):62-67.
赵明,孙伟健,陈丽杰,等.狼毒大戟地上部分化学成分研究[J].中草药, 2014, 45(19):2752-2756..
舒朋华,唐荣平,李军萍,等.禹白附化学成分研究[J].时珍国医国药, 2019, 30(5):1058-1060.
龚邦,战凯璇,周雨华,等.沙蓬地上部分化学成分的分离与鉴定(I)[J].中国现代中药, 2012, 14(10):7-11.
韦建华,李亚楠,莫惠雯,等.壮药龙脷叶化学成分的研究(I)[J].时珍国医国药, 2017, 28(2):289-291.
Cheng J, Yi X M, Wang Y H, et al. Phenolics from the roots of hairy fig(Ficus hirta Vahl.)exert prominent antiinflammatory activity[J]. J Funct Foods, 2017, 31:79-88.
Nhiem N X, Kiem P V, Minh C V, et al. Diarylheptanoids and flavonoids from Viscum album inhibit LPS-stimulated production of pro-inflammatory cytokines in bone marrow-derived dendritic cells[J]. J Nat Prod, 2013,76(4):495-502.
Bajpai V K, Alam M B, Quan K T, et al. Attenuation of inflammatory responses by(+)-syringaresinol via MAPKinase-mediated suppression of NF-κB signaling in vitro and in vivo[J]. Sci Rep, 2018, 8:9216.
Ziadlou R, Barbero A, Stoddart M J, et al. Regulation of inflammatory response in human osteoarthritic chondrocytes by novel herbal small molecules[J]. Int J Mol Sci, 2019, 20(22):5745.
Tsai Y C, Chen S H, Lin L C, et al. Anti-inflammatory principles from Sarcandra glabra[J]. J Agric Food Chem,2017, 65(31):6497-6505.
Yoo S R, Jeong S J, Lee N R, et al. Simultaneous determination and anti-inflammatory effects of four phenolic compounds in Dendrobii Herba[J]. Nat Prod Res, 2017, 31(24):2923-2926.)
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藏药黄帚橐吾化学成分研究
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中草药 | 化学成分 2026,57(9): 3274-3280
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中草药 |化学成分 2026 , 57 (9) : 3274 -3280
藏药黄帚橐吾化学成分研究
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王瑶1, 张馨予1, 廖佳慧1, 王洪玲1
作者信息
    1 江西中医药大学, 中药资源与民族药研究中心, 江西 南昌 330004
通讯作者:
王洪玲
作者简介:
王瑶: 王瑶(2002-),女,汉族,硕士研究生,主要从事中药尤其是民族药药效物质基础研究。E-mail:wangyao1@jxutcm.edu.cn
Chemical constituents of Tibetan medicine Ligularia virgaurea
  • WANG Yao, ZHANG Xinyu, LIAO Jiahui, WANG Hongling
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.09.002
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    目的 研究藏药黄帚橐吾Ligularia virgaurea的化学成分。方法 采用硅胶柱色谱、Sephadex LH-20、ODS反相柱色谱与半制备HPLC对黄帚橐吾进行分离纯化,结合NMR、MS等波谱学方法鉴定化合物结构。结果 从黄帚橐吾石油醚和醋酸乙酯部位中分离得到19个化合物,分别鉴定为1-[(1S,3aR,4R,7S,7aS)-4-羟基-4-羟甲基-7-异丙基-1,2,3,3a,5,6,7,7a-八氢茚-1-基]乙酮(1)、10α-hydroxy-1-oxoeremophila-7(11),8(9)-dien-12,8-olide(2)、6α,10α-dihydroxy-1-oxoeremophila-7(11),8(9)-dien-12,8-olide(3)、3-hydroxycacalolide(4)、6β-acetoxy-9-oxo-10αH-furanoeremophilane(5)、松脂醇(6)、皮树脂醇(7)、丁香脂素(8)、对羟基苯甲酸(9)、3,4-二羟基苯甲酸甲酯(10)、丁香酸(syringic acid,11)、3,4,5-三甲氧基苯甲酸(3,4,5-trimethoxybenzoic acid,12)、邻苯二甲酸二甲酯(13)、紫丁香苷(14)、羽扇豆醇(15)、钝叶醇(16)、亚油酸乙酯(17)、15-十八碳烯酸(18)、10-二十碳烯酸(19)。结论 其中,化合物1为新化合物,命名为黄帚橐吾酮A(14-hydroxy-oplopanone);化合物5141619均为首次从黄帚橐吾中分离得到。
    藏药  /  黄帚橐吾  /  黄帚橐吾酮A  /  松脂醇  /  皮树脂醇  /  紫丁香苷  /  15-十八碳烯酸
    Objective To investigate the chemical constituents of Tibetan medicine Ligularia virgaurea. Methods The compounds were isolated and purified by silica gel column chromatography, Sephadex LH-20, ODS reversed-phase column chromatography and semi-preparative HPLC, and the structures were identified by spectral data (NMR and MS). Results A total of 19 compounds were isolated and identified as follows 1-[(1S,3aR,4R,7S,7aS)-4-hydroxy-4-hydroxymethyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone (1), 10α-hydroxy-1-oxoeremophila-7(11),8(9)-dien-12,8-olide (2), 6α,10α-dihydroxy-1-oxoeremophila-7(11),8(9)-dien-12,8-olide (3), 3-hydroxycacalolide (4), 6β-acetoxy-9-oxo-10αH-furanoeremophilane (5), pinoresinol (6), medioresinol (7), syringaresinol (8), p-hydroxybenzoic acid (9), methyl 3,4-dihydroxybenzoate (10), syringic acid (11), 3,4,5-trimethoxybenzoic acid (12), dimethy phthalate (13), syringin (14)、lupeol (15), obtusifoliol (16), ethyl linoleate (17), 15-vaccenic acid (18), 10-eicosenoic acid (19). Conclusion Compound 1 is a new compound, designated 14-hydroxy-oplopanone. Compounds 514, 1619 are isolated from L. virgaurea for the first time.
    Tibetan medicine  /  Ligularia virgaurea (Maxim.) Mattf.  /  14-hydroxy-oplopanone  /  pinoresinol  /  medioresinol  /  syringin  /  15-vaccenic acid
    王瑶, 张馨予, 廖佳慧, 王洪玲. 藏药黄帚橐吾化学成分研究. 中草药, 2026 , 57 (9) : 3274 -3280 . DOI: 10.7501/j.issn.0253-2670.2026.09.002
    WANG Yao, ZHANG Xinyu, LIAO Jiahui, WANG Hongling. Chemical constituents of Tibetan medicine Ligularia virgaurea[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (9) : 3274 -3280 . DOI: 10.7501/j.issn.0253-2670.2026.09.002

      国家自然科学基金资助项目(U2202213);国家自然科学基金资助项目(32470428)

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    Marcelo D, Olov S, Nelson H. Furanoeremophilanes from Senecio clivicolus Weddell[J]. Bolivian J Chem, 2013,30(1):80-83.
    In S J, Seo K H, Song N Y, et al. Lignans and neolignans from the stems of Vibrunum erosum and their neuroprotective and anti-inflammatory activity[J]. Arch Pharmacal Res, 2015, 38(1):26-34.
    王威,刘小红,高华,等.东北铁线莲地上部位化学成分研究[J].中草药, 2014, 45(17):2440-2446
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    Fotie J, Bohle D S, Leimanis M L, et al. Lupeol long-chain fatty acid esters with antimalarial activity from Holarrhena floribunda[J]. J Nat Prod, 2006, 69(1):62-67.
    赵明,孙伟健,陈丽杰,等.狼毒大戟地上部分化学成分研究[J].中草药, 2014, 45(19):2752-2756..
    舒朋华,唐荣平,李军萍,等.禹白附化学成分研究[J].时珍国医国药, 2019, 30(5):1058-1060.
    龚邦,战凯璇,周雨华,等.沙蓬地上部分化学成分的分离与鉴定(I)[J].中国现代中药, 2012, 14(10):7-11.
    韦建华,李亚楠,莫惠雯,等.壮药龙脷叶化学成分的研究(I)[J].时珍国医国药, 2017, 28(2):289-291.
    Cheng J, Yi X M, Wang Y H, et al. Phenolics from the roots of hairy fig(Ficus hirta Vahl.)exert prominent antiinflammatory activity[J]. J Funct Foods, 2017, 31:79-88.
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    Bajpai V K, Alam M B, Quan K T, et al. Attenuation of inflammatory responses by(+)-syringaresinol via MAPKinase-mediated suppression of NF-κB signaling in vitro and in vivo[J]. Sci Rep, 2018, 8:9216.
    Ziadlou R, Barbero A, Stoddart M J, et al. Regulation of inflammatory response in human osteoarthritic chondrocytes by novel herbal small molecules[J]. Int J Mol Sci, 2019, 20(22):5745.
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    Yoo S R, Jeong S J, Lee N R, et al. Simultaneous determination and anti-inflammatory effects of four phenolic compounds in Dendrobii Herba[J]. Nat Prod Res, 2017, 31(24):2923-2926.
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    多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
    红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
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