Article(id=1304406870513447007, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406828071281069, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.02.002, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1762876800000, receivedDateStr=2025-11-12, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788924432637, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788924432637, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788924432637, creator=13701087609, updateTime=1788924432637, updator=13701087609, issue=Issue{id=1304406828071281069, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='2', pageStart='393', pageEnd='788', issueExtLink='null', onlineDate='null', pubDate='1769529600000', pubDateStr='2026-01-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788924422518, creator='13701087609', updateTime=1788924652596, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304407793138688830, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406828071281069, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304407793138688831, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304406828071281069, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=400, endPage=404, ext={EN=ArticleExt(id=1304406870832214113, articleId=1304406870513447007, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Two new trinorcycloartane triterpenoids from stems and leaves of Astragalus membranaceus, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical constituents and their anti-inflammatory activity of Cynanchum wilfordii. Methods Various chromatographic techniques including silica gel, ODS, and Sephadex LH-20 column chromatography were employed for the isolation and purification of compounds. Their structures were elucidated through comprehensive spectroscopic analysis including HR-ESI-MS, ESI-MS, 1H-NMR, 13C-NMR, HSQC, and HMBC. The anti-inflammatory activity of the compounds was evaluated using the Griess method. Results Two compounds were isolated and identified as (7'R,8'S)-dehydrodiconiferyl alcohol 9'-O-D-xylopyranoside (1) and 3β-[(O-D-glucopyranosyl)-oxy]-8β,14β-trihydroxycarda-5,20-(22)-dienolide (2). Compounds 1 and 2 inhibited NO production by 55.16% and 15.34%, respectively, with a median inhibition concentration (IC50) of 41.37 μmol/L for compound 1. Conclusion Compounds 1 and 2 are both new compounds, belonging to lignan and cardenolide types, respectively. They have been assigned the names cynawilforin A (1) and wilforcardenoside A (2). In vitro anti-inflammatory assays indicated that compound 1 exhibits certain anti-inflammatory activity., authors=ZHANG Luyuan, ZHOU Jing, LOU Hongbo, PU Kailiang, LI Yunlu, CHEN Chao, CHEN Yingfei, XU Xiaoyu, SHEN Yong, authorsList=ZHANG Luyuan, ZHOU Jing, LOU Hongbo, PU Kailiang, LI Yunlu, CHEN Chao, CHEN Yingfei, XU Xiaoyu, SHEN Yong, 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=1304406870744133728, articleId=1304406870513447007, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=隔山牛皮消中2个新化学成分研究, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究隔山牛皮消Cynanchum wilfordii的化学成分及其抗炎活性。方法 采用硅胶、ODS和Sephadex LH-20等多种色谱分离技术开展化合物的分离纯化,运用HR-ESI-MS、ESI-MS、¹H-NMR、¹³C-NMR、HSQC、HMBC多种波谱技术鉴定化合物结构;采用Griess法研究化合物的抗炎活性。结果 从隔山牛皮消块根中分离得到2个化合物,分别鉴定为(7'R,8'S)-dehydrodiconiferyl alcohol 9'-O-D-xylopyranoside(1)和3β-[(O-D-glucopyranosyloxy]-8β,14β-trihydroxycarda-5,20(22)-dienolide(2)。化合物12对NO生成的抑制率分别为55.16%和15.34%,化合物1的半数抑制浓度(median inhibition concentration,IC₅₀)为41.37 μmol/L。结论 化合物12均为新化合物,分别属于木脂素和强心苷类,分别命名为隔山牛皮消素A和隔山牛皮消强心苷A。体外抗炎实验表明,化合物1具有一定的抗炎活性。, authors=张露元1, 周晶1, 娄红波1, 普开亮1, 李云璐1, 陈超1, 陈英飞1, 徐笑宇1, 沈勇1,2, authorsList=张露元, 周晶, 娄红波, 普开亮, 李云璐, 陈超, 陈英飞, 徐笑宇, 沈勇, authorCompany=1 云南农业大学农学与生物技术学院, 云南 昆明 650201;
2 昆明康人生物科技有限公司, 云南 昆明 650000, correspAuthors=徐笑宇, authorNote=张露元: 张露元(2001—),女,硕士研究生,研究方向为药用植物资源化学开发利用。E-mail: 1483669890@qq.com 周晶: 周晶(1999—),男,硕士研究生,研究方向为药用植物资源化学开发利用。E-mail: 2320701463@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=Oavf2sCliFjYmJCGIaRo8w==, pdfFileSize=1702683, 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=云南省高校服务重点产业科技项目 (FWCY-QYCT2024014); 建设面向南亚东南亚科技创新中心专项项目 (202403AP140013))}, authors=null, keywords=[Keyword(id=1304406870974820450, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304406870513447007, language=CN, orderNo=1, keyword=隔山牛皮消), Keyword(id=1304406871046123619, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304406870513447007, language=CN, orderNo=2, keyword=木脂素), Keyword(id=1304406871125815396, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304406870513447007, language=CN, orderNo=3, keyword=强心苷), Keyword(id=1304406871205507173, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304406870513447007, language=CN, orderNo=4, keyword=抗炎活性), Keyword(id=1304406871272616038, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304406870513447007, language=CN, orderNo=5, keyword=隔山牛皮消素A), Keyword(id=1304406871356502119, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304406870513447007, language=CN, orderNo=6, keyword=隔山牛皮消强心苷A), Keyword(id=1304406873046806633, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304406870513447007, language=EN, orderNo=1, keyword=Cynanchum wilfordii(Maxim.) 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Petersen L M, Hoeck C, Frisvad J C, et al. Dereplication guided discovery of secondary metabolites of mixed biosynthetic origin from Aspergillus aculeatu[J]. Molecules, 2014, 19(8):10898-10921.
Shao C L, Wang C Y, Wei M Y, et al. Two new benzaldehyde derivatives from mangrove endophytic fungus (No. ZZF 32)[J]. Chem Nat Compd, 2009, 45(6):779-781.
Lei L R, Gong L Q, Jin M Y, et al. Research advances in the structures and biological activities of secondary metabolites from Talaromyces[J]. Front Microbiol, 2022, 13:984801.)
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隔山牛皮消中2个新化学成分研究
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中草药 | 化学成分 2026,57(2): 400-404
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中草药 |化学成分 2026 , 57 (2) : 400 -404
隔山牛皮消中2个新化学成分研究
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张露元1, 周晶1, 娄红波1, 普开亮1, 李云璐1, 陈超1, 陈英飞1, 徐笑宇1, 沈勇1,2
作者信息
    1 云南农业大学农学与生物技术学院, 云南 昆明 650201;
    2 昆明康人生物科技有限公司, 云南 昆明 650000
通讯作者:
徐笑宇
作者简介:
张露元: 张露元(2001—),女,硕士研究生,研究方向为药用植物资源化学开发利用。E-mail: 1483669890@qq.com 周晶: 周晶(1999—),男,硕士研究生,研究方向为药用植物资源化学开发利用。E-mail: 2320701463@qq.com
Two new trinorcycloartane triterpenoids from stems and leaves of Astragalus membranaceus
  • ZHANG Luyuan, ZHOU Jing, LOU Hongbo, PU Kailiang, LI Yunlu, CHEN Chao, CHEN Yingfei, XU Xiaoyu, SHEN Yong
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.02.002
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    目的 研究隔山牛皮消Cynanchum wilfordii的化学成分及其抗炎活性。方法 采用硅胶、ODS和Sephadex LH-20等多种色谱分离技术开展化合物的分离纯化,运用HR-ESI-MS、ESI-MS、¹H-NMR、¹³C-NMR、HSQC、HMBC多种波谱技术鉴定化合物结构;采用Griess法研究化合物的抗炎活性。结果 从隔山牛皮消块根中分离得到2个化合物,分别鉴定为(7'R,8'S)-dehydrodiconiferyl alcohol 9'-O-D-xylopyranoside(1)和3β-[(O-D-glucopyranosyloxy]-8β,14β-trihydroxycarda-5,20(22)-dienolide(2)。化合物12对NO生成的抑制率分别为55.16%和15.34%,化合物1的半数抑制浓度(median inhibition concentration,IC₅₀)为41.37 μmol/L。结论 化合物12均为新化合物,分别属于木脂素和强心苷类,分别命名为隔山牛皮消素A和隔山牛皮消强心苷A。体外抗炎实验表明,化合物1具有一定的抗炎活性。
    隔山牛皮消  /  木脂素  /  强心苷  /  抗炎活性  /  隔山牛皮消素A  /  隔山牛皮消强心苷A
    Objective To investigate the chemical constituents and their anti-inflammatory activity of Cynanchum wilfordii. Methods Various chromatographic techniques including silica gel, ODS, and Sephadex LH-20 column chromatography were employed for the isolation and purification of compounds. Their structures were elucidated through comprehensive spectroscopic analysis including HR-ESI-MS, ESI-MS, 1H-NMR, 13C-NMR, HSQC, and HMBC. The anti-inflammatory activity of the compounds was evaluated using the Griess method. Results Two compounds were isolated and identified as (7'R,8'S)-dehydrodiconiferyl alcohol 9'-O-D-xylopyranoside (1) and 3β-[(O-D-glucopyranosyl)-oxy]-8β,14β-trihydroxycarda-5,20-(22)-dienolide (2). Compounds 1 and 2 inhibited NO production by 55.16% and 15.34%, respectively, with a median inhibition concentration (IC50) of 41.37 μmol/L for compound 1. Conclusion Compounds 1 and 2 are both new compounds, belonging to lignan and cardenolide types, respectively. They have been assigned the names cynawilforin A (1) and wilforcardenoside A (2). In vitro anti-inflammatory assays indicated that compound 1 exhibits certain anti-inflammatory activity.
    Cynanchum wilfordii(Maxim.) Hemsl  /  lignan  /  cardenolide  /  anti-inflammatory activity  /  cynawilforin A  /  wilforcardenoside A
    张露元, 周晶, 娄红波, 普开亮, 李云璐, 陈超, 陈英飞, 徐笑宇, 沈勇. 隔山牛皮消中2个新化学成分研究. 中草药, 2026 , 57 (2) : 400 -404 . DOI: 10.7501/j.issn.0253-2670.2026.02.002
    ZHANG Luyuan, ZHOU Jing, LOU Hongbo, PU Kailiang, LI Yunlu, CHEN Chao, CHEN Yingfei, XU Xiaoyu, SHEN Yong. Two new trinorcycloartane triterpenoids from stems and leaves of Astragalus membranaceus[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (2) : 400 -404 . DOI: 10.7501/j.issn.0253-2670.2026.02.002

      云南省高校服务重点产业科技项目 (FWCY-QYCT2024014); 建设面向南亚东南亚科技创新中心专项项目 (202403AP140013)

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    Yang S W, Chan T M, Terracciano J, et al. A new hydrogenated azaphilone Sch 725680 from Aspergillus sp[J]. J Antibiot:Tokyo, 2006, 59(11):720-723.
    Petersen L M, Hoeck C, Frisvad J C, et al. Dereplication guided discovery of secondary metabolites of mixed biosynthetic origin from Aspergillus aculeatu[J]. Molecules, 2014, 19(8):10898-10921.
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    Lei L R, Gong L Q, Jin M Y, et al. Research advances in the structures and biological activities of secondary metabolites from Talaromyces[J]. Front Microbiol, 2022, 13:984801.
    2026年第57卷第2期
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    doi: 10.7501/j.issn.0253-2670.2026.02.002
    • 接收时间:2025-11-12
    • 首发时间:2026-09-09
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    2种不同金属材料的力学参数

    Family
    属数
    Number of
    genus
    种数
    Number of
    species
    占总种数比例
    Percentage of
    total species (%)

    Genus
    种数
    Number of
    species
    占总种数比例
    Percentage of total
    species (%)
    鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
    小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
    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
    小菇属 Mycena 11 5.26
    光柄菇属 Pluteus 5 2.39
    红菇属 Russula 17 8.13
    栓菌属 Trametes 5 2.39
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