Article(id=1276976153155989525, tenantId=1146029695717560320, journalId=1276577828834349082, issueId=1276976057215488893, articleNumber=null, orderNo=null, doi=10.19540/j.cnki.cjcmm.20251010.202, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1749657600000, receivedDateStr=2025-06-12, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1782384439982, onlineDateStr=2026-06-25, pubDate=1768406400000, pubDateStr=2026-01-15, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1782384439982, onlineIssueDateStr=2026-06-25, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1782384439982, creator=13701087609, updateTime=1782384439982, 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=450, endPage=455, ext={EN=ArticleExt(id=1276976153340538903, articleId=1276976153155989525, tenantId=1146029695717560320, journalId=1276577828834349082, language=EN, title=A new chlorinated butenolide from endophytic fungus Aspergillus sp. FH-1 of Valeriana officinalis, columnId=null, journalTitle=Chinese Journal of Traditional Chinese Medicine, columnName=null, runingTitle=null, highlight=null, articleAbstract=

This study aims to investigate the antifungal secondary metabolites produced by the endophytic fungus Aspergillus sp. FH-1 isolated from Valeriana officinalis via a high-salt rice medium. Compounds were isolated and purified by silica gel and ODS column chromatography, semi-preparative HPLC, and other techniques. The chemical structures were elucidated through analysis of physicochemical properties and spectroscopic data of nuclear magnetic resonance (NMR), infrared (IR), and mass spectrometry (MS). The inhibitory effects of all the compounds against Colletotrichum gloeosporioides were evaluated via the mycelial growth rate method. Eight compounds were obtained from the ethyl acetate extract of Aspergillus sp. FH-1. They were identified as asperchoried A (1), butyrolactone Ⅱ (2), isobutyrolactone Ⅱ (3), aspernolide A (4), butyrolactone Ⅴ (5), clavatone (6), 1-hydroxy-6,8-dimethoxy-3-methylanthracene-9,10-dione (7), and (S) -7-methoxy-2, 5-dimethyl-2, 3-dihydrobenzofuran-6-ol (8). Among them, compound 1 is a novel chlorinated butanolide derivative and was designated asperchoried A. Compounds 1, 2, 6, and 7 possessed inhibitory effects on C. gloeosporioides, with EC50 values of 15.08, 77.19, 89.94, and 62.02 μg·mL-1, respectively.

, authors=null, authorsList=Hao FAN, Xin WANG, Meng-xin YU, Yi-xuan WU, Li-yuan ZHAO, Ke-zhen ZHANG, Yu-ze LI, Wei WANG, Xiao-mei SONG, Dong-dong ZHANG, authorCompany=null, correspAuthors=Dong-dong ZHANG, 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=1276976153567031321, articleId=1276976153155989525, tenantId=1146029695717560320, journalId=1276577828834349082, language=CN, title=缬草药材内生真菌Aspergillus sp. FH-1中1个新的氯代丁烯内酯类化合物, columnId=1276976014295167305, journalTitle=中国中药杂志, columnName=化学, runingTitle=null, highlight=null, articleAbstract=

研究缬草药材内生真菌Aspergillus sp. FH-1大米高盐培养基中抗真菌次生代谢产物及其抗菌活性。采用硅胶和ODS柱色谱以及半制备液相色谱等方法进行分离纯化,并结合其理化性质及NMR、IR、MS等波谱学技术进行结构解析。采用菌丝生长速率法测定所有化合物对番木瓜炭疽病菌Colletotrichum gloeosporioides的抗真菌活性。从Aspergillus sp. FH-1菌株的乙酸乙酯提取部位分离得到8个化合物,分别鉴定为asperchoried A(1)、butyrolactone Ⅱ(2)、isobutyrolactone Ⅱ(3)、aspernolide A(4)、butyrolactone Ⅴ(5)、clavatone(6)、1-羟基-6,8-二甲氧基-3-甲基蒽-9,10-二酮(7)、(S)-7-甲氧基-2,5-二甲基-2,3-二氢苯并呋喃-6-醇(8),其中化合物1为氯代丁烯内酯类新化合物。化合物1267抑制番木瓜炭疽病菌活性的EC50分别为15.08、77.19、89.94、62.02 μg·mL-1,表现出抑制番木瓜炭疽病菌活性。

, authors=

樊浩,博士,实验师,主要从事中草药药效物质基础研究,E-mail:

, authorsList=樊浩, 王鑫, 禹梦欣, 吴怡轩, 赵丽媛, 张可桢, 李玉泽, 王薇, 宋小妹, 张东东, authorCompany=null, correspAuthors=张东东, authorNote=null, correspAuthorsNote=

*

张东东,博士,副教授,硕士生导师,主要从事中药药效物质基础研究,E-mail:
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樊浩,博士,实验师,主要从事中草药药效物质基础研究,E-mail:

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缬草药材内生真菌Aspergillus sp. FH-1中1个新的氯代丁烯内酯类化合物
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樊浩 , 王鑫 , 禹梦欣 , 吴怡轩 , 赵丽媛 , 张可桢 , 李玉泽 , 王薇 , 宋小妹 , 张东东 *
中国中药杂志 | 化学 2026,51(2): 450-455
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中国中药杂志 |化学 2026 , 51 (2) : 450 -455
缬草药材内生真菌Aspergillus sp. FH-1中1个新的氯代丁烯内酯类化合物
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药学院 陕西省太白七药研究与应用重点研究室,陕西 咸阳 712046)])])]
樊浩 , 王鑫, 禹梦欣, 吴怡轩, 赵丽媛, 张可桢, 李玉泽, 王薇, 宋小妹, 张东东*
作者信息
  • 陕西中医药大学 药学院 陕西省太白七药研究与应用重点研究室,陕西 咸阳 712046
通讯作者:

*

张东东,博士,副教授,硕士生导师,主要从事中药药效物质基础研究,E-mail:
A new chlorinated butenolide from endophytic fungus Aspergillus sp. FH-1 of Valeriana officinalis
Hao FAN , Xin WANG, Meng-xin YU, Yi-xuan WU, Li-yuan ZHAO, Ke-zhen ZHANG, Yu-ze LI, Wei WANG, Xiao-mei SONG, Dong-dong ZHANG*
Affiliations
  • Shaanxi Key Laboratory of Research and Application of "Taibai Qi Yao", School of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang 712046, China
出版时间: 2026-01-15 doi: 10.19540/j.cnki.cjcmm.20251010.202
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研究缬草药材内生真菌Aspergillus sp. FH-1大米高盐培养基中抗真菌次生代谢产物及其抗菌活性。采用硅胶和ODS柱色谱以及半制备液相色谱等方法进行分离纯化,并结合其理化性质及NMR、IR、MS等波谱学技术进行结构解析。采用菌丝生长速率法测定所有化合物对番木瓜炭疽病菌Colletotrichum gloeosporioides的抗真菌活性。从Aspergillus sp. FH-1菌株的乙酸乙酯提取部位分离得到8个化合物,分别鉴定为asperchoried A(1)、butyrolactone Ⅱ(2)、isobutyrolactone Ⅱ(3)、aspernolide A(4)、butyrolactone Ⅴ(5)、clavatone(6)、1-羟基-6,8-二甲氧基-3-甲基蒽-9,10-二酮(7)、(S)-7-甲氧基-2,5-二甲基-2,3-二氢苯并呋喃-6-醇(8),其中化合物1为氯代丁烯内酯类新化合物。化合物1267抑制番木瓜炭疽病菌活性的EC50分别为15.08、77.19、89.94、62.02 μg·mL-1,表现出抑制番木瓜炭疽病菌活性。

缬草  /  Aspergillus sp. FH-1  /  分离纯化  /  结构鉴定  /  asperchoried A  /  抗真菌

This study aims to investigate the antifungal secondary metabolites produced by the endophytic fungus Aspergillus sp. FH-1 isolated from Valeriana officinalis via a high-salt rice medium. Compounds were isolated and purified by silica gel and ODS column chromatography, semi-preparative HPLC, and other techniques. The chemical structures were elucidated through analysis of physicochemical properties and spectroscopic data of nuclear magnetic resonance (NMR), infrared (IR), and mass spectrometry (MS). The inhibitory effects of all the compounds against Colletotrichum gloeosporioides were evaluated via the mycelial growth rate method. Eight compounds were obtained from the ethyl acetate extract of Aspergillus sp. FH-1. They were identified as asperchoried A (1), butyrolactone Ⅱ (2), isobutyrolactone Ⅱ (3), aspernolide A (4), butyrolactone Ⅴ (5), clavatone (6), 1-hydroxy-6,8-dimethoxy-3-methylanthracene-9,10-dione (7), and (S) -7-methoxy-2, 5-dimethyl-2, 3-dihydrobenzofuran-6-ol (8). Among them, compound 1 is a novel chlorinated butanolide derivative and was designated asperchoried A. Compounds 1, 2, 6, and 7 possessed inhibitory effects on C. gloeosporioides, with EC50 values of 15.08, 77.19, 89.94, and 62.02 μg·mL-1, respectively.

Valeriana officinalis  /  Aspergillus sp. FH-1  /  isolation and purification  /  structural elucidation  /  asperchoried A  /  antifungal effect
樊浩, 王鑫, 禹梦欣, 吴怡轩, 赵丽媛, 张可桢, 李玉泽, 王薇, 宋小妹, 张东东. 缬草药材内生真菌Aspergillus sp. FH-1中1个新的氯代丁烯内酯类化合物. 中国中药杂志, 2026 , 51 (2) : 450 -455 . DOI: 10.19540/j.cnki.cjcmm.20251010.202
Hao FAN, Xin WANG, Meng-xin YU, Yi-xuan WU, Li-yuan ZHAO, Ke-zhen ZHANG, Yu-ze LI, Wei WANG, Xiao-mei SONG, Dong-dong ZHANG. A new chlorinated butenolide from endophytic fungus Aspergillus sp. FH-1 of Valeriana officinalis[J]. Chinese Journal of Traditional Chinese Medicine, 2026 , 51 (2) : 450 -455 . DOI: 10.19540/j.cnki.cjcmm.20251010.202
  • 国家中医药管理局重点学科项目(zyyzdxk-2023202)
  • 秦创原中医药产业创新聚集区项目(L2024-QCY-ZYYJJQ-X81)
  • 陕西中医药大学创新团队项目(2023-CXTD-05)
  • 大学生创新训练计划项目(S202510716010)
  • 陕西省教育厅科学研究项目(25JK0430)
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2026年第51卷第2期
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doi: 10.19540/j.cnki.cjcmm.20251010.202
  • 接收时间:2025-06-12
  • 首发时间:2026-06-25
  • 出版时间:2026-01-15
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  • 收稿日期:2025-06-12
基金
国家中医药管理局重点学科项目(zyyzdxk-2023202)
秦创原中医药产业创新聚集区项目(L2024-QCY-ZYYJJQ-X81)
陕西中医药大学创新团队项目(2023-CXTD-05)
大学生创新训练计划项目(S202510716010)
陕西省教育厅科学研究项目(25JK0430)
作者信息
    陕西中医药大学 药学院 陕西省太白七药研究与应用重点研究室,陕西 咸阳 712046

通讯作者:

*

张东东,博士,副教授,硕士生导师,主要从事中药药效物质基础研究,E-mail:
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https://castjournals.cast.org.cn/joweb/zgzyzz/CN/10.19540/j.cnki.cjcmm.20251010.202
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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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