Article(id=1322631196530561117, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631195876242221, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.17.003, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1775491200000, receivedDateStr=2026-04-07, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793269450552, onlineDateStr=2026-10-29, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793269450552, onlineIssueDateStr=2026-10-29, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793269450552, creator=13701087609, updateTime=1793269450552, updator=13701087609, issue=Issue{id=1322631195876242221, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='17', pageStart='6661', pageEnd='7072', issueExtLink='null', onlineDate='null', pubDate='1789142400000', pubDateStr='2026-09-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1793269450396, creator='13701087609', updateTime=1793269538381, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322631565008556693, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631195876242221, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322631565008556694, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631195876242221, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=6677, endPage=6681, ext={EN=ArticleExt(id=1322631196815773791, articleId=1322631196530561117, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Two new naphthoquinones from leaves of Tectona grandis and their antifungal activity, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical constituents of the leaves of Tectona grandis , and search for antifungal active ingredients. Methods The compounds were obtained by silica gel, MCI, and prep-HPLC column chromatography. Their structures were identified by HRESIMS, IR, 1D- and 2D NMR analysis. The isolates were tested for their antifungal activity by 96 well plate microbroth dilution method. Results Two new naphthoquinones, (E )-2,5,8-trihydroxy-3-(4-acetoxy-3-methylbut-2-en-1-yl)-1,4-naphthoquinone (1 ) and (E )-2,5,8-trihydroxy-3-(4-hydroxy-3-methylbut-2-en-1-yl)-1,4-naphthoquinone (2 ), were isolated from the 90% MeOH extract of the leaves of T. grandis . Compounds 1 and 2 exhibited significant antifungal activity when combined with fluconazole, against fluconazole-resistant Candida albicans with MIC50 values of 3.28 and 5.32 μg/mL, respectively. Conclusion Compounds 1 and 2 , named tectonagrandiones A and B, were two new naphthoquinones, and the naphthoquinones might be the active antifungal constituents from T. grandis ., authors=HUANG Chunqiu1 , DI-RI Ke-La2 , QUAN Yongjie2 , DU Wenhao2 , YANG Ye3 , ZUO Aixue2 , XIAO Yan4 , JIANG Zhiyong2 , authorsList=HUANG Chunqiu, DI-RI Ke-La, QUAN Yongjie, DU Wenhao, YANG Ye, ZUO Aixue, XIAO Yan, JIANG Zhiyong, authorCompany=1 Academy of Yunnan Botanical Pharmaceutical Co., Ltd,, Kunming 650500, China; 2 Yunnan University of Chinese Medicine, Key Laboratory of Dai and Yi Medicines in Yunnan Province, Key Laboratory of Modern Research on Ethnic Medicine in Yunnan Provincial Universities, Kunming 650500, China; 3 School of Life Science and Technology, Kunming University of Science & Technology, Kunming 650500, China; 4 Kunming Medical University, Kunming 650500, China, 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=1322631196744470622, articleId=1322631196530561117, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=柚木中2个新的萘醌及其抗真菌活性, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 对柚木Tectona grandis 枝叶进行化学成分研究,寻找其中抗真菌活性成分。方法 采用正反相硅胶柱色谱、MCI、Sephadex LH-20柱色谱以及半制备高效液相色谱等分离手段进行分离纯化,根据HRESIMS、IR、1D和2D NMR等波谱数据和理化性质对化合物进行结构鉴定。采用96孔板微量肉汤稀释法评价其抗真菌活性。结果 从柚木枝叶90%乙醇提取物的石油醚萃取部分中分离鉴定了2个新的萘醌类化合物,分别为 (E )-2,5,8-trihydroxy-3-(4-acetoxy-3-methylbut-2-en-1-yl)-1,4-naphthoquinone(1 )和 (E )-2,5,8-trihydroxy-3-(4-hydroxy-3-methylbut-2-en-1-yl)-1,4-naphthoquinone(2 )。2个化合物均表现出显著的氟康唑(fluconazole,FLC)耐药白色念珠菌抑制活性,与FLC联用时对FLC耐药白色念珠菌的50%最低抑菌浓度(minimum inhibitory concentration,MIC₅₀)值分别为3.28、5.32 μg/mL。结论 化合物1 和2 均为新的萘醌类化合物,分别命名为柚木萘醌A和柚木萘醌B;均具有显著的抗真菌活性。, authors=黄春球1 , 的日克拉2 , 全咏洁2 , 杜文豪2 , 杨野3 , 左爱学2 , 肖艳4 , 江志勇2 , authorsList=黄春球, 的日克拉, 全咏洁, 杜文豪, 杨野, 左爱学, 肖艳, 江志勇, authorCompany=1 云南植物药业有限公司研究院, 云南 昆明 650500; 2 云南中医药大学云南省傣医药彝医药重点实验室 云南省高校民族药现代研究重点实验室, 云南 昆明 650500; 3 昆明理工大学生命科学与技术学院, 云南 昆明 650500; 4 昆明医科大学, 云南昆明 650500, correspAuthors=江志勇, authorNote=黄春球: 黄春球,副研究员,研究方向为药物化学。E-mail:1556231631@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=hxR/sQtWGUZ0KkxwD445Dw==, pdfFileSize=927210, 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=国家自然科学基金项目 (82360688); 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pdfUrlEn=https://castjournals.cast.org.cn/joweb/zcy/EN/PDF/10.7501/j.issn.0253-2670.2026.17.003, aliStartDate=null, aliEndDate=null, collectionFlag=false, citedCount=null, citedUrl=null, previewStatus=0, delFlag=0, hasFullText=0, orderTime=1789142400000, fullTextJson=null, articleText=null, reference=中国科学院中国植物志编辑委员会. 中国植物志(第三十一卷) [M]. 北京: 科学出版社, 1982: 80. 王西洋, 黄桂华, 杨光, 等. 柚木的植物化学与药理学研究进展[J]. 林业与环境科学, 2020, 36(2): 122-132. Dégbé M, Debierre-Grockiego F, Tété-Bénissan A, et al. Extracts of Tectona grandis and Vernonia amygdalina have anti-toxoplasma and pro-inflammatory properties in vitro [J]. Parasite, 2018, 25: 11. Asdaq S M B, Nayeem N, Abida, et al. Tectona grandis L.f: A comprehensive review on its patents, chemical constituents, and biological activities [J]. Saudi J Biol Sci, 2022, 29(3): 1456-1464. Singh N, Dixit K, Kumar K. Pharmacological, and phytochemical profile of Tectona grandis linn (Verbenaceae) – A comprehensive review [J]. Afr J Bio Sci, 2024, 6(13): 6182-6196. Qiu H Y, Liu R, Long L. Analysis of chemical composition of extractives by acetone and the chromatic aberration of teak (Tectona grandis L.F.) from China [J]. Molecules, 2019, 24(10): 1989. Macías F A, Lacret R, Varela R M, et al. Bioactive apocarotenoids from Tectona grandis [J]. Phytochemistry, 2008, 69(15): 2708-2715. Kopa T K, Tchinda A T, Tala M F, et al. Antiplasmodial anthraquinones and hemisynthetic derivatives from the leaves of Tectona grandis (Verbenaceae) [J]. Phytochem Lett, 2014, 8: 41-45. Feroj Hasan A F M, Furumoto T, Begum S, et al. Hydroxysesamone and 2,3-epoxysesamone from roots of Sesamum indicum [J]. Phytochemistry, 2001, 58(8): 1225-1228. Jiang Z Y, Feng J E, Duan L K, et al. Tigliane diterpenoids with larvicidal, antifungal, and α-glucosidase inhibitory activities from Croton damayeshu [J]. J Nat Prod, 2022, 85(2): 405-414. Demarco P V, Farkas E, Doddrell D, et al. Pyridine-induced solvent shifts in the nuclear magnetic resonance spectra of hydroxylic compounds [J]. J Am Chem Soc, 1968, 90(20): 5480-5486. Mantsch H H, Smith I C P. A study of solvent effects on the 13 C nuclear magnetic resonance spectra of cholesterol, pyridine, and uridine [J]. Can J Chem, 1973, 51(9): 1384-1391.)
中草药
|化学成分
2026
, 57
(17) :
6677
-6681
柚木中2个新的萘醌及其抗真菌活性
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黄春球1 , 的日克拉2 , 全咏洁2 , 杜文豪2 , 杨野3 , 左爱学2 , 肖艳4 , 江志勇2
作者信息
1 云南植物药业有限公司研究院, 云南 昆明 650500; 2 云南中医药大学云南省傣医药彝医药重点实验室 云南省高校民族药现代研究重点实验室, 云南 昆明 650500; 3 昆明理工大学生命科学与技术学院, 云南 昆明 650500; 4 昆明医科大学, 云南昆明 650500
通讯作者:
江志勇
作者简介:
黄春球: 黄春球,副研究员,研究方向为药物化学。E-mail:1556231631@qq.com
Two new naphthoquinones from leaves of Tectona grandis and their antifungal activity
HUANG Chunqiu1 , DI-RI Ke-La2 , QUAN Yongjie2 , DU Wenhao2 , YANG Ye3 , ZUO Aixue2 , XIAO Yan4 , JIANG Zhiyong2
Affiliations
1 Academy of Yunnan Botanical Pharmaceutical Co., Ltd,, Kunming 650500, China; 2 Yunnan University of Chinese Medicine, Key Laboratory of Dai and Yi Medicines in Yunnan Province, Key Laboratory of Modern Research on Ethnic Medicine in Yunnan Provincial Universities, Kunming 650500, China; 3 School of Life Science and Technology, Kunming University of Science & Technology, Kunming 650500, China; 4 Kunming Medical University, Kunming 650500, China
doi: 10.7501/j.issn.0253-2670.2026.17.003
文章导航
目的 对柚木Tectona grandis 枝叶进行化学成分研究,寻找其中抗真菌活性成分。方法 采用正反相硅胶柱色谱、MCI、Sephadex LH-20柱色谱以及半制备高效液相色谱等分离手段进行分离纯化,根据HRESIMS、IR、1D和2D NMR等波谱数据和理化性质对化合物进行结构鉴定。采用96孔板微量肉汤稀释法评价其抗真菌活性。结果 从柚木枝叶90%乙醇提取物的石油醚萃取部分中分离鉴定了2个新的萘醌类化合物,分别为 (E )-2,5,8-trihydroxy-3-(4-acetoxy-3-methylbut-2-en-1-yl)-1,4-naphthoquinone(1 )和 (E )-2,5,8-trihydroxy-3-(4-hydroxy-3-methylbut-2-en-1-yl)-1,4-naphthoquinone(2 )。2个化合物均表现出显著的氟康唑(fluconazole,FLC)耐药白色念珠菌抑制活性,与FLC联用时对FLC耐药白色念珠菌的50%最低抑菌浓度(minimum inhibitory concentration,MIC₅₀)值分别为3.28、5.32 μg/mL。结论 化合物1 和2 均为新的萘醌类化合物,分别命名为柚木萘醌A和柚木萘醌B;均具有显著的抗真菌活性。
柚木
/
马鞭草科
/
萘醌
/
抗真菌活性
/
柚木萘醌A
/
柚木萘醌B
Objective To investigate the chemical constituents of the leaves of Tectona grandis , and search for antifungal active ingredients. Methods The compounds were obtained by silica gel, MCI, and prep-HPLC column chromatography. Their structures were identified by HRESIMS, IR, 1D- and 2D NMR analysis. The isolates were tested for their antifungal activity by 96 well plate microbroth dilution method. Results Two new naphthoquinones, (E )-2,5,8-trihydroxy-3-(4-acetoxy-3-methylbut-2-en-1-yl)-1,4-naphthoquinone (1 ) and (E )-2,5,8-trihydroxy-3-(4-hydroxy-3-methylbut-2-en-1-yl)-1,4-naphthoquinone (2 ), were isolated from the 90% MeOH extract of the leaves of T. grandis . Compounds 1 and 2 exhibited significant antifungal activity when combined with fluconazole, against fluconazole-resistant Candida albicans with MIC50 values of 3.28 and 5.32 μg/mL, respectively. Conclusion Compounds 1 and 2 , named tectonagrandiones A and B, were two new naphthoquinones, and the naphthoquinones might be the active antifungal constituents from T. grandis .
Tectona grandis L.
/
Verbenaceae
/
naphthoquinones
/
antifungal activity
/
tectonagrandiones A
/
tectonagrandiones B
黄春球, 的日克拉, 全咏洁, 杜文豪, 杨野, 左爱学, 肖艳, 江志勇.
柚木中2个新的萘醌及其抗真菌活性.
中草药,
2026
, 57
(17)
: 6677
-6681
.
DOI: 10.7501/j.issn.0253-2670.2026.17.003
HUANG Chunqiu, DI-RI Ke-La, QUAN Yongjie, DU Wenhao, YANG Ye, ZUO Aixue, XIAO Yan, JIANG Zhiyong.
Two new naphthoquinones from leaves of Tectona grandis and their antifungal activity[J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(17)
: 6677
-6681
.
DOI: 10.7501/j.issn.0253-2670.2026.17.003
国家自然科学基金项目 (82360688); 云南省中医药联合专项重点项目 (202101AZ070001-164); 云南省教育厅高原特色民族药用植物研究科技创新团队; 国家中医药管理局高水平中医药重点学科建设项目-傣药学 (Zyyzdxk-2023192)
参考文献
引证文献
中国科学院中国植物志编辑委员会. 中国植物志(第三十一卷) [M]. 北京: 科学出版社, 1982: 80. 王西洋, 黄桂华, 杨光, 等. 柚木的植物化学与药理学研究进展[J]. 林业与环境科学, 2020, 36(2): 122-132. Dégbé M, Debierre-Grockiego F, Tété-Bénissan A, et al. Extracts of Tectona grandis and Vernonia amygdalina have anti-toxoplasma and pro-inflammatory properties in vitro [J]. Parasite, 2018, 25: 11. Asdaq S M B, Nayeem N, Abida, et al. Tectona grandis L.f: A comprehensive review on its patents, chemical constituents, and biological activities [J]. Saudi J Biol Sci, 2022, 29(3): 1456-1464. Singh N, Dixit K, Kumar K. Pharmacological, and phytochemical profile of Tectona grandis linn (Verbenaceae) – A comprehensive review [J]. Afr J Bio Sci, 2024, 6(13): 6182-6196. Qiu H Y, Liu R, Long L. Analysis of chemical composition of extractives by acetone and the chromatic aberration of teak (Tectona grandis L.F.) from China [J]. Molecules, 2019, 24(10): 1989. Macías F A, Lacret R, Varela R M, et al. Bioactive apocarotenoids from Tectona grandis [J]. Phytochemistry, 2008, 69(15): 2708-2715. Kopa T K, Tchinda A T, Tala M F, et al. Antiplasmodial anthraquinones and hemisynthetic derivatives from the leaves of Tectona grandis (Verbenaceae) [J]. Phytochem Lett, 2014, 8: 41-45. Feroj Hasan A F M, Furumoto T, Begum S, et al. Hydroxysesamone and 2,3-epoxysesamone from roots of Sesamum indicum [J]. Phytochemistry, 2001, 58(8): 1225-1228. Jiang Z Y, Feng J E, Duan L K, et al. Tigliane diterpenoids with larvicidal, antifungal, and α-glucosidase inhibitory activities from Croton damayeshu [J]. J Nat Prod, 2022, 85(2): 405-414. Demarco P V, Farkas E, Doddrell D, et al. Pyridine-induced solvent shifts in the nuclear magnetic resonance spectra of hydroxylic compounds [J]. J Am Chem Soc, 1968, 90(20): 5480-5486. Mantsch H H, Smith I C P. A study of solvent effects on the 13 C nuclear magnetic resonance spectra of cholesterol, pyridine, and uridine [J]. Can J Chem, 1973, 51(9): 1384-1391.
2026年第57卷第17期
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doi: 10.7501/j.issn.0253-2670.2026.17.003
接收时间:2026-04-07
首发时间:2026-10-29
https://castjournals.cast.org.cn/joweb/zcy/CN/10.7501/j.issn.0253-2670.2026.17.003
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2种不同金属材料的力学参数
科 Family 属数 Number of genus 种数 Number of species 占总种数比例 Percentage of total species (%) 属 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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