Article(id=1304388247577191250, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388135723496407, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.13.002, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1777478400000, receivedDateStr=2026-04-30, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788919992584, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788919992584, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788919992584, creator=13701087609, updateTime=1788919992584, updator=13701087609, issue=Issue{id=1304388135723496407, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='13', pageStart='4949', pageEnd='5352', issueExtLink='null', onlineDate='null', pubDate='1783785600000', pubDateStr='2026-07-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788919965916, creator='13701087609', updateTime=1788923489765, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304402915871977875, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388135723496407, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304402915871977876, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388135723496407, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=4964, endPage=4968, ext={EN=ArticleExt(id=1304388247900152660, articleId=1304388247577191250, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Two new diphenyl ethers from Cyperus rotundus , columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical constituents and their antitumor activities isolated from Cyperus rotundus . Methods The isolates were isolated and purified by silica gel, Sephadex gel, reversed-phase C18 column chromatography, and semi-preparative high-performance liquid chromatography (HPLC). The structures of the obtained compounds were elucidated by spectroscopic methods such as nuclear magnetic resonance (NMR) and mass spectrometry (MS). Finally, all compounds were subjected to MTT assays to evaluate their anti-tumor activities. Results Two new diphenyl ethers were obtained from C. rotundus , specifically as 2,3′-dihydroxy-5,2′,5′-trimethoxy diphenyl ether (1 ) and 2,3′-dihydroxy-4,2′,5′-trimethoxy diphenyl ether (2 ). Both compounds exhibited moderate inhibitory effects on human colon cancer cell line HCT116, with median inhibition concentration (IC50 ) values of (24.20 ± 0.77) and (25.26 ± 0.65) μmol/L, respectively. Conclusion Compounds 1 and 2 are new compounds with anti-tumor potential, named cydipethers A (1 ) and B (2 ). Diphenyl ethers were identified from C. rotundus for the first time., authors=HU Yali, LIU Qingyun, WANG Ruyuan, authorsList=HU Yali, LIU Qingyun, WANG Ruyuan, 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=1304388247820460883, articleId=1304388247577191250, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=香附中2个新的二苯醚类化合物, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究香附Cyperus rotundus 的化学成分及其抗肿瘤活性。方法 采用硅胶柱色谱、反相C₁₈柱色谱、凝胶柱色谱、半制备高效液相色谱等技术进行分离纯化,再通过核磁共振、质谱等波谱学手段鉴定结构,最后通过MTT法对分离的化合物进行抗肿瘤细胞毒性测定。结果 从中药香附中分离得到了2个新的二苯醚类化合物,分别鉴定为2,3′-二羟基-5,2′,5′-三甲氧基二苯醚(1 )和2,3′-二羟基-4,2′,5′-三甲氧基二苯醚(2 );二者对人源结肠癌细胞HCT116表现出一定的抑制作用,半数抑制浓度(median inhibition concentration,IC₅₀)值分别为(24.20±0.77)μmol/L和(25.26±0.65)μmol/L。结论 化合物1 和2 均为新化合物,分别命名为香附二苯醚A(1 )和香附二苯醚B(2 ),并具有一定的抗肿瘤潜力。二苯醚类为首次从香附中分离得到的新结构类群化合物。, authors=胡雅丽1 , 刘青云1 , 汪汝渊1 , authorsList=胡雅丽, 刘青云, 汪汝渊, authorCompany=1 云南大学附属医院, 云南昆明 650021, correspAuthors=null, authorNote=胡雅丽: 胡雅丽(1993—),女,博士,主管药师,研究方向为天然药物化学。E-mail:807478014@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=2Vd0xJeMVgGlBQNmkA2KAw==, pdfFileSize=825992, 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=云南省教育厅科学研究基金项目-青年人才基础研究专项 (2025J0009); 云南大学医学科研基金-青年项目 (YDYXJJ2024-0050))}, authors=null, keywords=[Keyword(id=1304401943279988741, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388247577191250, language=CN, orderNo=1, keyword=莎草科), Keyword(id=1304401943376457734, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388247577191250, language=CN, orderNo=2, keyword=香附), Keyword(id=1304401943456149511, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388247577191250, language=CN, orderNo=3, keyword=二苯醚), Keyword(id=1304401943531646984, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388247577191250, language=CN, orderNo=4, keyword=抗肿瘤), Keyword(id=1304401943615533065, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388247577191250, language=CN, orderNo=5, keyword=香附二苯醚A), Keyword(id=1304401943678447626, tenantId=1146029695717560320, 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aliStartDate=null, aliEndDate=null, collectionFlag=false, citedCount=null, citedUrl=null, previewStatus=0, delFlag=0, hasFullText=0, orderTime=1788919992584, fullTextJson=null, articleText=null, reference=林永水. 中国植物志 (第四十卷) [M]. 北京: 科学出版社, 1994. 中国药典 [S]. 一部. 2025: 278. 王凤霞, 钱琪, 李葆林, 等. 香附化学成分和药理作用研究进展及质量标志物 (Q-Marker) 预测分析 [J]. 中草药, 2022, 53(16): 5225-5234. 张玉萱, 李医明. 基于UPLC-Q-Exactive Orbitrap-MS分析香附化学成分 [J]. 中华中医药杂志, 2025, 40(6): 3111-3117. 韩建卫, 孙延平, 杨炳友, 等. 香附的化学成分及其体外抗炎活性研究 [J]. 中南药学, 2024, 22(2): 322-328. 付琳, 王伟明. 香附化学成分及药理作用研究进展 [J]. 中医药学报, 2025, 53(8): 120-124. 许娜, 梁媛媛, 李文兵, 等. 香附挥发油研究进展 [J]. 中成药, 2022, 44(6): 1882-1888. 王培辰, 陈飞翔, 马双双, 等. 香附抗肿瘤作用机制研究进展 [J]. 中成药, 2025, 47(9): 3011-3020. Wang F K, Song X, Ma S S, et al . The treatment role of Cyperus rotundus L. to triple-negative breast cancer cells [J]. Biosci Rep , 2019, 39(6): BSR20190502. Mohamed A I, Beseni B K, Msomi N Z, et al . The antioxidant and antidiabetic potentials of polyphenolic-rich extracts of Cyperus rotundus (Linn.) [J]. J Biomol Struct Dyn , 2022, 40(22): 12075-12087. Babiaka S B, Moumbock A F A, Günther S, et al . Natural products in Cyperus rotundus L. (Cyperaceae): An update of the chemistry and pharmacological activities [J]. RSC Adv , 2021, 11(25): 15060-15077. 陈元惠, 罗霄, 廖婉, 等. 基于CiteSpace可视化图谱分析香附的研究动态及热点 [J]. 中草药, 2025, 56(5): 1717-1730. 乔俊昊, 杨颜溶, 孙静洋, 等. 基于HPLC指纹图谱结合化学模式识别及多指标成分定量评价香附质量 [J]. 中草药, 2024, 55(17): 5999-6008. Dechakhamphu A, Wongchum N, Chumroenphat T, et al . In vitro and in vivo evaluation for antioxidant and anti-diabetic properties of Cyperus rotundus L. kombucha [J]. Foods , 2023, 12(22): 4059. Wang Y N, Mou Y H, Dong Y, et al . Diphenyl ethers from a marine-derived Aspergillus sydowii [J]. Mar Drugs , 2018, 16(11): 451. 张梦雨, 刘娇, 刘畅, 等. 穿心草全草中两个新的二苯醚类化合物 [J]. 药学学报, 2024, 59(12): 3335-3341. Liu B, Wang Y X, Chen N, et al . Diphenyl ethers: Isolation, bioactivities and biosynthesis [J]. Mini Rev Org Chem , 2024, 21(6): 590-598. Hu Y L, Yue G G, Li X R, et al . Structurally diverse spirocyclic polycyclic polyprenylated acylphloroglucinols from Hypericum ascyron Linn. and their anti-tumor activity [J]. Phytochemistry , 2023, 212: 113727. Yan X T, An Z, Tang D, et al . Hyperelatosides A–E, biphenyl ether glycosides from Hypericum elatoides , with neurotrophic activity [J]. RSC Adv , 2018, 8(47): 26646-26655. 吴正治, 魏江春, 金星漂, 等. 一种异戊烯基间苯三酚醚类化合物及其制备方法和应用: 中国, CN119143699B [P]. 2025-05-16.)
中草药
|化学成分
2026
, 57
(13) :
4964
-4968
香附中2个新的二苯醚类化合物
全屏
胡雅丽1 , 刘青云1 , 汪汝渊1
作者信息
作者简介:
胡雅丽: 胡雅丽(1993—),女,博士,主管药师,研究方向为天然药物化学。E-mail:807478014@qq.com
Two new diphenyl ethers from Cyperus rotundus
HU Yali, LIU Qingyun, WANG Ruyuan
Affiliations
doi: 10.7501/j.issn.0253-2670.2026.13.002
文章导航
目的 研究香附Cyperus rotundus 的化学成分及其抗肿瘤活性。方法 采用硅胶柱色谱、反相C₁₈柱色谱、凝胶柱色谱、半制备高效液相色谱等技术进行分离纯化,再通过核磁共振、质谱等波谱学手段鉴定结构,最后通过MTT法对分离的化合物进行抗肿瘤细胞毒性测定。结果 从中药香附中分离得到了2个新的二苯醚类化合物,分别鉴定为2,3′-二羟基-5,2′,5′-三甲氧基二苯醚(1 )和2,3′-二羟基-4,2′,5′-三甲氧基二苯醚(2 );二者对人源结肠癌细胞HCT116表现出一定的抑制作用,半数抑制浓度(median inhibition concentration,IC₅₀)值分别为(24.20±0.77)μmol/L和(25.26±0.65)μmol/L。结论 化合物1 和2 均为新化合物,分别命名为香附二苯醚A(1 )和香附二苯醚B(2 ),并具有一定的抗肿瘤潜力。二苯醚类为首次从香附中分离得到的新结构类群化合物。
莎草科
/
香附
/
二苯醚
/
抗肿瘤
/
香附二苯醚A
/
香附二苯醚B
Objective To investigate the chemical constituents and their antitumor activities isolated from Cyperus rotundus . Methods The isolates were isolated and purified by silica gel, Sephadex gel, reversed-phase C18 column chromatography, and semi-preparative high-performance liquid chromatography (HPLC). The structures of the obtained compounds were elucidated by spectroscopic methods such as nuclear magnetic resonance (NMR) and mass spectrometry (MS). Finally, all compounds were subjected to MTT assays to evaluate their anti-tumor activities. Results Two new diphenyl ethers were obtained from C. rotundus , specifically as 2,3′-dihydroxy-5,2′,5′-trimethoxy diphenyl ether (1 ) and 2,3′-dihydroxy-4,2′,5′-trimethoxy diphenyl ether (2 ). Both compounds exhibited moderate inhibitory effects on human colon cancer cell line HCT116, with median inhibition concentration (IC50 ) values of (24.20 ± 0.77) and (25.26 ± 0.65) μmol/L, respectively. Conclusion Compounds 1 and 2 are new compounds with anti-tumor potential, named cydipethers A (1 ) and B (2 ). Diphenyl ethers were identified from C. rotundus for the first time.
Cyperaceae
/
Cyperus rotundus L.
/
diphenyl ether
/
antitumor
/
cydipethers A
/
cydipethers B
胡雅丽, 刘青云, 汪汝渊.
香附中2个新的二苯醚类化合物.
中草药,
2026
, 57
(13)
: 4964
-4968
.
DOI: 10.7501/j.issn.0253-2670.2026.13.002
HU Yali, LIU Qingyun, WANG Ruyuan.
Two new diphenyl ethers from Cyperus rotundus [J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(13)
: 4964
-4968
.
DOI: 10.7501/j.issn.0253-2670.2026.13.002
参考文献
引证文献
林永水. 中国植物志 (第四十卷) [M]. 北京: 科学出版社, 1994. 中国药典 [S]. 一部. 2025: 278. 王凤霞, 钱琪, 李葆林, 等. 香附化学成分和药理作用研究进展及质量标志物 (Q-Marker) 预测分析 [J]. 中草药, 2022, 53(16): 5225-5234. 张玉萱, 李医明. 基于UPLC-Q-Exactive Orbitrap-MS分析香附化学成分 [J]. 中华中医药杂志, 2025, 40(6): 3111-3117. 韩建卫, 孙延平, 杨炳友, 等. 香附的化学成分及其体外抗炎活性研究 [J]. 中南药学, 2024, 22(2): 322-328. 付琳, 王伟明. 香附化学成分及药理作用研究进展 [J]. 中医药学报, 2025, 53(8): 120-124. 许娜, 梁媛媛, 李文兵, 等. 香附挥发油研究进展 [J]. 中成药, 2022, 44(6): 1882-1888. 王培辰, 陈飞翔, 马双双, 等. 香附抗肿瘤作用机制研究进展 [J]. 中成药, 2025, 47(9): 3011-3020. Wang F K, Song X, Ma S S, et al . The treatment role of Cyperus rotundus L. to triple-negative breast cancer cells [J]. Biosci Rep , 2019, 39(6): BSR20190502. Mohamed A I, Beseni B K, Msomi N Z, et al . The antioxidant and antidiabetic potentials of polyphenolic-rich extracts of Cyperus rotundus (Linn.) [J]. J Biomol Struct Dyn , 2022, 40(22): 12075-12087. Babiaka S B, Moumbock A F A, Günther S, et al . Natural products in Cyperus rotundus L. (Cyperaceae): An update of the chemistry and pharmacological activities [J]. RSC Adv , 2021, 11(25): 15060-15077. 陈元惠, 罗霄, 廖婉, 等. 基于CiteSpace可视化图谱分析香附的研究动态及热点 [J]. 中草药, 2025, 56(5): 1717-1730. 乔俊昊, 杨颜溶, 孙静洋, 等. 基于HPLC指纹图谱结合化学模式识别及多指标成分定量评价香附质量 [J]. 中草药, 2024, 55(17): 5999-6008. Dechakhamphu A, Wongchum N, Chumroenphat T, et al . In vitro and in vivo evaluation for antioxidant and anti-diabetic properties of Cyperus rotundus L. kombucha [J]. Foods , 2023, 12(22): 4059. Wang Y N, Mou Y H, Dong Y, et al . Diphenyl ethers from a marine-derived Aspergillus sydowii [J]. Mar Drugs , 2018, 16(11): 451. 张梦雨, 刘娇, 刘畅, 等. 穿心草全草中两个新的二苯醚类化合物 [J]. 药学学报, 2024, 59(12): 3335-3341. Liu B, Wang Y X, Chen N, et al . Diphenyl ethers: Isolation, bioactivities and biosynthesis [J]. Mini Rev Org Chem , 2024, 21(6): 590-598. Hu Y L, Yue G G, Li X R, et al . Structurally diverse spirocyclic polycyclic polyprenylated acylphloroglucinols from Hypericum ascyron Linn. and their anti-tumor activity [J]. Phytochemistry , 2023, 212: 113727. Yan X T, An Z, Tang D, et al . Hyperelatosides A–E, biphenyl ether glycosides from Hypericum elatoides , with neurotrophic activity [J]. RSC Adv , 2018, 8(47): 26646-26655. 吴正治, 魏江春, 金星漂, 等. 一种异戊烯基间苯三酚醚类化合物及其制备方法和应用: 中国, CN119143699B [P]. 2025-05-16.
2026年第57卷第13期
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doi: 10.7501/j.issn.0253-2670.2026.13.002
接收时间:2026-04-30
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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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