Article(id=1276976181564019336, tenantId=1146029695717560320, journalId=1276577828834349082, issueId=1276976057215488893, articleNumber=null, orderNo=null, doi=10.19540/j.cnki.cjcmm.20251009.202, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1748275200000, receivedDateStr=2025-05-27, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1782384446754, onlineDateStr=2026-06-25, pubDate=1768406400000, pubDateStr=2026-01-15, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1782384446754, onlineIssueDateStr=2026-06-25, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1782384446754, creator=13701087609, updateTime=1782384446754, updator=13701087609, issue=Issue{id=1276976057215488893, tenantId=1146029695717560320, journalId=1276577828834349082, year='2026', volume='51', issue='2', pageStart='301', pageEnd='600', issueExtLink='null', onlineDate='null', pubDate='1768406400000', pubDateStr='2026-01-15', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=1, specialIssue=null, createTime=1782384417107, creator='13701087609', updateTime=1782384524478, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1276976507658563977, tenantId=1146029695717560320, journalId=1276577828834349082, issueId=1276976057215488893, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1276976507658563978, tenantId=1146029695717560320, journalId=1276577828834349082, issueId=1276976057215488893, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=444, endPage=449, ext={EN=ArticleExt(id=1276976181752763018, articleId=1276976181564019336, tenantId=1146029695717560320, journalId=1276577828834349082, language=EN, title=Secondary metabolites from Rhododendron molle endophyte Penicillium sp. RM and their inhibitory effects on tumor cell proliferation, columnId=null, journalTitle=Chinese Journal of Traditional Chinese Medicine, columnName=null, runingTitle=null, highlight=null, articleAbstract=

This study investigated the secondary metabolites of the endophytic fungus Penicillium sp. RM isolated from the toxic plant Rhododendron molle. Ten compounds were isolated and purified from the ethyl acetate extract of the fungal fermentation broth by silica gel column chromatography, gel column chromatography, and semi-preparative HPLC. The structures of these compounds were elucidated by comprehensive spectroscopic analyses, including NMR, MS, UV, IR, and CD. The identified compounds were as follows: penicidienone A (1), diversonol (2), alternariol (3), alternariol 9-methyl ether (4), methylated dechloromonilicin (5), norliquexantona (6), alternethanoxin A (7), α-diversonolic ester (8), (±) -asperlone A (9), and verruculotoxin (10). Compound 1 was identified as a new cyclopentenone derivative. Compound 9 showed inhibitory activity against the proliferation of HepG2 (IC50=9.7 μmol·L-1), HGC27 (IC50 = 9.3 μmol·L-1), and U251 (IC50 = 8.4 μmol·L-1) cell lines.

, authors=null, authorsList=Xue WANG, Lei ZHOU, Yi-hang HU, Yang LIU, Xue ZHANG, Yun-bao LIU, authorCompany=null, correspAuthors=Xue ZHANG, Yun-bao LIU, 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=1276976182017004172, articleId=1276976181564019336, tenantId=1146029695717560320, journalId=1276577828834349082, language=CN, title=羊踯躅内生真菌Penicillium sp. RM的次生代谢产物及其肿瘤细胞增殖抑制活性研究, columnId=1276976014295167305, journalTitle=中国中药杂志, columnName=化学, runingTitle=null, highlight=null, articleAbstract=

对羊踯躅内生真菌Penicillium sp. RM的次级代谢产物进行研究,采用硅胶柱色谱、凝胶柱色谱、半制备液相色谱等进行分离纯化,共从Penicillium sp. RM发酵物的乙酸乙酯部位中分离鉴定出10个化合物,利用NMR、MS、UV、IR、CD等现代波谱技术确定了化合物的结构,分别为penicidienone A(1)、diversonol(2)、alternariol(3)、alternariol 9-methyl ether(4)、methylated dechloromonilicin(5)、norliquexantona(6)、alternethanoxin A(7)、α-diversonolic ester(8)、(±)-asperlone A(9)、verruculotoxin (10),其中化合物1是1种新的环戊烯酮衍生物。肿瘤细胞增殖抑制活性筛选结果表明化合物9对HepG2、HGC27、U251细胞具有抑制作用,IC50分别为9.7、9.3、8.4 μmol·L-1

, authors=

王雪,硕士研究生,E-mail:

, authorsList=王雪, 周磊, 胡倚航, 刘洋, 张雪, 刘云宝, authorCompany=null, correspAuthors=张雪, 刘云宝, authorNote=null, correspAuthorsNote=

*

刘云宝,研究员,主要从事特殊生境微生物中新颖结构活性分子的发现及其形成机制研究,Tel:(010)83162679,E-mail:

*

张雪,副教授,主要从事药用植物内生真菌和根际真菌活性次级代谢产物及作用机制研究、中药和天然药物活性成分及质量控制研究,Tel:(024)43520730,E-mail:
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王雪,硕士研究生,E-mail:

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羊踯躅内生真菌Penicillium sp. RM的次生代谢产物及其肿瘤细胞增殖抑制活性研究
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王雪 1 , 周磊 1 , 胡倚航 1 , 刘洋 2 , 张雪 1, * , 刘云宝 2, *
中国中药杂志 | 化学 2026,51(2): 444-449
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中国中药杂志 |化学 2026 , 51 (2) : 444 -449
羊踯躅内生真菌Penicillium sp. RM的次生代谢产物及其肿瘤细胞增殖抑制活性研究
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王雪1 , 周磊1, 胡倚航1, 刘洋2, 张雪1, * , 刘云宝2, *
作者信息
  • 1.沈阳药科大学 中药学院,辽宁 沈阳 110016
  • 2.中国医学科学院 北京协和医学院 药物研究所 天然药物活性物质与功能国家重点实验室,北京 100050
通讯作者:

*

刘云宝,研究员,主要从事特殊生境微生物中新颖结构活性分子的发现及其形成机制研究,Tel:(010)83162679,E-mail:

*

张雪,副教授,主要从事药用植物内生真菌和根际真菌活性次级代谢产物及作用机制研究、中药和天然药物活性成分及质量控制研究,Tel:(024)43520730,E-mail:
Secondary metabolites from Rhododendron molle endophyte Penicillium sp. RM and their inhibitory effects on tumor cell proliferation
Xue WANG1 , Lei ZHOU1, Yi-hang HU1, Yang LIU2, Xue ZHANG1, * , Yun-bao LIU2, *
Affiliations
  • 1.School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, China
  • 2.State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
出版时间: 2026-01-15 doi: 10.19540/j.cnki.cjcmm.20251009.202
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对羊踯躅内生真菌Penicillium sp. RM的次级代谢产物进行研究,采用硅胶柱色谱、凝胶柱色谱、半制备液相色谱等进行分离纯化,共从Penicillium sp. RM发酵物的乙酸乙酯部位中分离鉴定出10个化合物,利用NMR、MS、UV、IR、CD等现代波谱技术确定了化合物的结构,分别为penicidienone A(1)、diversonol(2)、alternariol(3)、alternariol 9-methyl ether(4)、methylated dechloromonilicin(5)、norliquexantona(6)、alternethanoxin A(7)、α-diversonolic ester(8)、(±)-asperlone A(9)、verruculotoxin (10),其中化合物1是1种新的环戊烯酮衍生物。肿瘤细胞增殖抑制活性筛选结果表明化合物9对HepG2、HGC27、U251细胞具有抑制作用,IC50分别为9.7、9.3、8.4 μmol·L-1

羊踯躅  /  内生真菌  /  Penicillium sp. RM  /  次生代谢产物  /  环戊烯酮

This study investigated the secondary metabolites of the endophytic fungus Penicillium sp. RM isolated from the toxic plant Rhododendron molle. Ten compounds were isolated and purified from the ethyl acetate extract of the fungal fermentation broth by silica gel column chromatography, gel column chromatography, and semi-preparative HPLC. The structures of these compounds were elucidated by comprehensive spectroscopic analyses, including NMR, MS, UV, IR, and CD. The identified compounds were as follows: penicidienone A (1), diversonol (2), alternariol (3), alternariol 9-methyl ether (4), methylated dechloromonilicin (5), norliquexantona (6), alternethanoxin A (7), α-diversonolic ester (8), (±) -asperlone A (9), and verruculotoxin (10). Compound 1 was identified as a new cyclopentenone derivative. Compound 9 showed inhibitory activity against the proliferation of HepG2 (IC50=9.7 μmol·L-1), HGC27 (IC50 = 9.3 μmol·L-1), and U251 (IC50 = 8.4 μmol·L-1) cell lines.

Rhododendron molle  /  endophytic fungi  /  Penicillium sp. RM  /  secondary metabolites  /  cyclopentenone derivative
王雪, 周磊, 胡倚航, 刘洋, 张雪, 刘云宝. 羊踯躅内生真菌Penicillium sp. RM的次生代谢产物及其肿瘤细胞增殖抑制活性研究. 中国中药杂志, 2026 , 51 (2) : 444 -449 . DOI: 10.19540/j.cnki.cjcmm.20251009.202
Xue WANG, Lei ZHOU, Yi-hang HU, Yang LIU, Xue ZHANG, Yun-bao LIU. Secondary metabolites from Rhododendron molle endophyte Penicillium sp. RM and their inhibitory effects on tumor cell proliferation[J]. Chinese Journal of Traditional Chinese Medicine, 2026 , 51 (2) : 444 -449 . DOI: 10.19540/j.cnki.cjcmm.20251009.202

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doi: 10.19540/j.cnki.cjcmm.20251009.202
  • 接收时间:2025-05-27
  • 首发时间:2026-06-25
  • 出版时间:2026-01-15
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  • 收稿日期:2025-05-27
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    1.沈阳药科大学 中药学院,辽宁 沈阳 110016
    2.中国医学科学院 北京协和医学院 药物研究所 天然药物活性物质与功能国家重点实验室,北京 100050

通讯作者:

*

刘云宝,研究员,主要从事特殊生境微生物中新颖结构活性分子的发现及其形成机制研究,Tel:(010)83162679,E-mail:

*

张雪,副教授,主要从事药用植物内生真菌和根际真菌活性次级代谢产物及作用机制研究、中药和天然药物活性成分及质量控制研究,Tel:(024)43520730,E-mail:
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https://castjournals.cast.org.cn/joweb/zgzyzz/CN/10.19540/j.cnki.cjcmm.20251009.202
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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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