Article(id=1304415019161113104, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414997581427653, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.08.013, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1771344000000, receivedDateStr=2026-02-18, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788926375426, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788926375426, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788926375426, creator=13701087609, updateTime=1788926375426, updator=13701087609, issue=Issue{id=1304414997581427653, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='8', pageStart='2877', pageEnd='3260', issueExtLink='null', onlineDate='null', pubDate='1777305600000', pubDateStr='2026-04-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788926370282, creator='13701087609', updateTime=1788926758667, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304416626649096991, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414997581427653, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304416626649096992, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414997581427653, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=3000, endPage=3005, ext={EN=ArticleExt(id=1304415019484074514, articleId=1304415019161113104, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Study on phenylpropanoids in whole plant from Ferula bungeana , columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To clarify the chemical constituents of the petroleum ether extract from the whole plant of Ferula bungeana . Methods The chemical constituents of petroleum ether extract from the whole plant of F. bungeana were studied using classical silica gel column chromatography and thin-layer chromatography. The spectral data of the isolated compounds were analyzed to determine their structures. Meanwhile, by examining the effect of the isolated compounds on nitric oxide (NO) release in the culture medium of RAW264.7 macrophages induced by lipopolysaccharide (LPS), their inhibitory effect on inflammatory responses was evaluated. Results From the petroleum ether extract of F. bungeana whole plant, eight compounds were isolated and identified as 1-isoprenyloxy-1-(3'-hydroxy-4',5'-methylenedioxy)phenyl-2-angeloyloxy-phenylpropane (1 ), myristicin (2 ), crocatone (3 ), diversivittatin (4 ), 2-epilaserine (5 ), 1-hydroxy-1-(3' -methoxy-4' ,5' -methylenedioxy)-phenylpropane (6 ), 1-hydroxy-1-(3' ,4' -methylenedioxy-2' ,5' -dimethoxy)-phenylpropane (7 ), 1-carbonyl-1-(3' -hydroxy-4' ,5' -methylenedioxy)-phenylpropane (8 ). The activity screening results showed that compounds 1 , 4 , and 5 exhibited good NO inhibitory activity at a concentration of 10 μmol/L, with inhibition rates of 78.5%, 85.9%, and 79.0%, respectively. Conclusions Compound 1 is a new compound, named ferubundiester; Compounds 2 and 5 were isolated from F. bungeana for the first time, and compounds 4 —8 were obtained from plants of the Ferula genus for the first time. Compounds 1 , 4 , and 5 exhibit similar potent anti-inflammatory activity., authors=WANG Qinghu, GAO Qingshan, WANG Haiying, Na-ren-chao-ke-tu, authorsList=WANG Qinghu, GAO Qingshan, WANG Haiying, Na-ren-chao-ke-tu, 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=1304415019408577041, articleId=1304415019161113104, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=砂茴香全草中苯丙烷类化学成分研究, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究砂茴香Ferula bungeana 全草石油醚提取物的化学成分。方法 运用经典硅胶柱色谱及薄层色谱对砂茴香全草石油醚提取物的化学成分进行研究,并对分离得到化合物的波谱数据进行分析,确定其结构。同时,通过考察分离得到化合物对脂多糖(lipopolysaccharide,LPS)诱导的小鼠RAW264.7巨噬细胞培养液中一氧化氮(NO)释放量的影响,评价其对炎症反应的抑制作用。结果 从砂茴香全草石油醚提取物中分离鉴定了8个苯丙烷类化合物,分别为1-异戊烯酰氧基-1-(3' -羟基-4' ,5' -亚甲二氧基)苯基-2-当归酰氧基丙烷(1 )、肉豆蔻醚(2 )、深黄水芹酮(3 )、diversivittatin(4 )、2-epilaserine(5 )、1-羟基-1-(3' -甲氧基-4' ,5' -亚甲二氧基)苯基丙烷(6 )、1-羟基-1-(3' ,4' -亚甲二氧基-2' ,5' -二甲氧基)苯基丙烷(7 )、1-羰基-1-(3' -羟基-4' ,5' -亚甲二氧基)苯基丙烷(8 )。活性筛选结果显示,在10 μmol/L浓度下,化合物1 、4 和5 具有良好的NO抑制活性,其抑制率分别为78.5%、85.9%和79.0%。结论 化合物1 为新化合物,命名为砂茴香二酯;化合物2 和3 为首次从砂茴香中分离得到,而化合物4 ~8 均为首次从阿魏属植物中分离得到。化合物1 、4 和5 具有良好的抗炎活性。, authors=王青虎1 , 高青山1 , 王海英2 , 那仁朝克图1 , authorsList=王青虎, 高青山, 王海英, 那仁朝克图, authorCompany=1 内蒙古民族大学蒙医药学院, 内蒙古 通辽 028000; 2 内蒙古民族大学附属医院, 内蒙古 通辽 028000, correspAuthors=null, authorNote=王青虎: 王青虎,教授,博士生导师,从事蒙药有效物质基础及其药理研究。E-mail:wqh693@163.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, 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totalCitationFrequency=null, icpCode=null, psCode=null, advertisingLicenseCode=null, copyrightInformation=null, country=null, option=, provinceCode=null, provinceName=null, collectFlag=false, interPubPlatform=, interPubPlatformUrl=null), detailUrlCn=https://castjournals.cast.org.cn/joweb/zcy/CN/10.7501/j.issn.0253-2670.2026.08.013, detailUrlEn=https://castjournals.cast.org.cn/joweb/zcy/EN/10.7501/j.issn.0253-2670.2026.08.013, pdfUrlCn=https://castjournals.cast.org.cn/joweb/zcy/CN/PDF/10.7501/j.issn.0253-2670.2026.08.013, pdfUrlEn=https://castjournals.cast.org.cn/joweb/zcy/EN/PDF/10.7501/j.issn.0253-2670.2026.08.013, aliStartDate=null, aliEndDate=null, collectionFlag=false, citedCount=null, citedUrl=null, previewStatus=0, delFlag=0, hasFullText=0, orderTime=1788926375426, fullTextJson=null, articleText=null, reference=王路, 孙睿, 徐萌, 等. 阿魏化学成分、药理作用及毒理研究进展[J]. 世界中医药, 2020, 15(24):3887-3894. 杨秀伟. 阿魏属药用植物的物质基础[J]. 中国现代中药, 2018, 20(2):123-144. 邢亚超, 李宁, 薛洁. 阿魏属植物化学成分研究进展[J]. 沈阳药科大学学报, 2012, 29(9):730-741. Xing Y C, Li N, Zhou D, et al. Sesquiterpene coumarins from Ferula sinkiangensis act as neuroinflammation inhibitors[J]. Planta Med, 2017, 83(1/2):135-142. Teng L, Ma G Z, Li L, et al. Karatavicinol a, a new anti-ulcer sesquiterpene coumarin from Ferula sinkiangensis[J]. Chem Nat Compd, 2013, 49(4):606-609. 高源, 邢亚超, 郭俐含, 等. 新疆阿魏树脂不同极性部位对人肺癌细胞的体外抑制作用研究[J]. 现代药物与临床, 2015, 30(4):366-369. Li G Z, Wang J C, Li X J, et al. An unusual sesquiterpene coumarin from the seeds of Ferula sinkiangensis[J]. J Asian Nat Prod Res, 2016, 18(9):891-896. Ye B G, Wang S, Zhang L. Studies on the detoxification effects and acute toxicity of a mixture of cis-sec-butyl-1-propoenyl disulphide and trans-sec-butyl-1-propoenyl disulphide isolated from crude essential oil of Ferula sinkiangensis K.M. Shen, a Chinese traditional herbal medicine[J]. Nat Prod Res, 2011, 25(12):1161-1170. 王光明, 朝梁, 宋亚伟, 等. 砂茴香化学成分研究[J]. 中国药学杂志, 2024, 59(23):2216-2225. Kang X R, Wu L L, Zhao C L, et al. A new sesquiterpene coumarins from Ferula bungeana Kitagawa[J]. Nat Prod Res, 2025, 39(14):4112-4116. Yang R L, Yan Z H, Lu Y. Cytotoxic phenylpropanoids from carrot[J]. J Agric Food Chem, 2008, 56(9):3024-3027. You C X, Jiang H Y, Zhang W J, et al. Contact toxicity and repellency of the main components from the essential oil of Clausena anisum-olens against two stored product insects[J]. J Insect Sci, 2015, 15(1):87. Babekov A U, Khasanova K I, Eshbakova K A, et al. Chemical constituents of Ferula lapidosa[J]. Chem Nat Compd, 2024, 60(1):177-179. Iranshahi M, Hosseini S T, Sahebkar A H, et al. Diversivittatin, a new phenylpropanoid derivative from the roots of Ferula diversivittata[J]. Chem Nat Compd, 2010, 46(2):192-194. Zhang M M, Kamoldinov K S, Kodirova D R, et al. Chemical constituents from Ferula samarkandica[J]. Chem Nat Compd, 2024, 60(2):367-370. Sreedhar E, Sateesh Chandra Kumar R, Venkateswar Reddy G, et al. The first total synthesis of neohelmanticins A-D, amino derivatives of the 1, 2-dihydroxypropane core and biological evaluation[J]. Tetrahedron Asymmetry, 2009, 20(4):440-448. Sreedhar E, Sateesh Chandra Kumar R, Venkateswar Reddy G, et al. The first total synthesis of neohelmanticins A-D, amino derivatives of the 1, 2-dihydroxypropane core and biological evaluation[J]. Tetrahedron Asymmetry, 2009, 20(4):440-448. Xue G M, Xue J F, Zhao C G, et al. Sesquiterpenoids from Artemisia argyi and their NO production inhibitory activity in RAW264.7 cells[J]. Nat Prod Res, 2021, 35(17):2887-2894. 贾瑶瑶, 冯好, 刘艺, 等. 黑风藤中一个新的降桉叶烷型倍半萜[J]. 药学学报, 2025, 60(9):2858-2862.)
中草药
|化学成分
2026
, 57
(8) :
3000
-3005
砂茴香全草中苯丙烷类化学成分研究
全屏
王青虎1 , 高青山1 , 王海英2 , 那仁朝克图1
作者信息
1 内蒙古民族大学蒙医药学院, 内蒙古 通辽 028000; 2 内蒙古民族大学附属医院, 内蒙古 通辽 028000
作者简介:
王青虎: 王青虎,教授,博士生导师,从事蒙药有效物质基础及其药理研究。E-mail:wqh693@163.com
Study on phenylpropanoids in whole plant from Ferula bungeana
WANG Qinghu, GAO Qingshan, WANG Haiying, Na-ren-chao-ke-tu
Affiliations
doi: 10.7501/j.issn.0253-2670.2026.08.013
文章导航
目的 研究砂茴香Ferula bungeana 全草石油醚提取物的化学成分。方法 运用经典硅胶柱色谱及薄层色谱对砂茴香全草石油醚提取物的化学成分进行研究,并对分离得到化合物的波谱数据进行分析,确定其结构。同时,通过考察分离得到化合物对脂多糖(lipopolysaccharide,LPS)诱导的小鼠RAW264.7巨噬细胞培养液中一氧化氮(NO)释放量的影响,评价其对炎症反应的抑制作用。结果 从砂茴香全草石油醚提取物中分离鉴定了8个苯丙烷类化合物,分别为1-异戊烯酰氧基-1-(3' -羟基-4' ,5' -亚甲二氧基)苯基-2-当归酰氧基丙烷(1 )、肉豆蔻醚(2 )、深黄水芹酮(3 )、diversivittatin(4 )、2-epilaserine(5 )、1-羟基-1-(3' -甲氧基-4' ,5' -亚甲二氧基)苯基丙烷(6 )、1-羟基-1-(3' ,4' -亚甲二氧基-2' ,5' -二甲氧基)苯基丙烷(7 )、1-羰基-1-(3' -羟基-4' ,5' -亚甲二氧基)苯基丙烷(8 )。活性筛选结果显示,在10 μmol/L浓度下,化合物1 、4 和5 具有良好的NO抑制活性,其抑制率分别为78.5%、85.9%和79.0%。结论 化合物1 为新化合物,命名为砂茴香二酯;化合物2 和3 为首次从砂茴香中分离得到,而化合物4 ~8 均为首次从阿魏属植物中分离得到。化合物1 、4 和5 具有良好的抗炎活性。
阿魏属
/
砂茴香
/
苯丙烷类
/
砂茴香二酯
/
肉豆蔻醚
/
深黄水芹酮
/
抗炎活性
Objective To clarify the chemical constituents of the petroleum ether extract from the whole plant of Ferula bungeana . Methods The chemical constituents of petroleum ether extract from the whole plant of F. bungeana were studied using classical silica gel column chromatography and thin-layer chromatography. The spectral data of the isolated compounds were analyzed to determine their structures. Meanwhile, by examining the effect of the isolated compounds on nitric oxide (NO) release in the culture medium of RAW264.7 macrophages induced by lipopolysaccharide (LPS), their inhibitory effect on inflammatory responses was evaluated. Results From the petroleum ether extract of F. bungeana whole plant, eight compounds were isolated and identified as 1-isoprenyloxy-1-(3'-hydroxy-4',5'-methylenedioxy)phenyl-2-angeloyloxy-phenylpropane (1 ), myristicin (2 ), crocatone (3 ), diversivittatin (4 ), 2-epilaserine (5 ), 1-hydroxy-1-(3' -methoxy-4' ,5' -methylenedioxy)-phenylpropane (6 ), 1-hydroxy-1-(3' ,4' -methylenedioxy-2' ,5' -dimethoxy)-phenylpropane (7 ), 1-carbonyl-1-(3' -hydroxy-4' ,5' -methylenedioxy)-phenylpropane (8 ). The activity screening results showed that compounds 1 , 4 , and 5 exhibited good NO inhibitory activity at a concentration of 10 μmol/L, with inhibition rates of 78.5%, 85.9%, and 79.0%, respectively. Conclusions Compound 1 is a new compound, named ferubundiester; Compounds 2 and 5 were isolated from F. bungeana for the first time, and compounds 4 —8 were obtained from plants of the Ferula genus for the first time. Compounds 1 , 4 , and 5 exhibit similar potent anti-inflammatory activity.
Ferula genus
/
Ferula bungeana l Kitagawa
/
phenylpropanoids
/
ferubundiester
/
myristicin
/
crocatone
/
anti-inflammatory activity
王青虎, 高青山, 王海英, 那仁朝克图.
砂茴香全草中苯丙烷类化学成分研究.
中草药,
2026
, 57
(8)
: 3000
-3005
.
DOI: 10.7501/j.issn.0253-2670.2026.08.013
WANG Qinghu, GAO Qingshan, WANG Haiying, Na-ren-chao-ke-tu.
Study on phenylpropanoids in whole plant from Ferula bungeana [J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(8)
: 3000
-3005
.
DOI: 10.7501/j.issn.0253-2670.2026.08.013
内蒙古自治区自然科学基金项目 (2025QN08004); 内蒙古自治区教育厅一流学科专项项目 (YLXKZX-NMD-004); 蒙药研发国家地方联合工程研究中心开放基金项目 (MDK2024010)
参考文献
引证文献
王路, 孙睿, 徐萌, 等. 阿魏化学成分、药理作用及毒理研究进展[J]. 世界中医药, 2020, 15(24):3887-3894. 杨秀伟. 阿魏属药用植物的物质基础[J]. 中国现代中药, 2018, 20(2):123-144. 邢亚超, 李宁, 薛洁. 阿魏属植物化学成分研究进展[J]. 沈阳药科大学学报, 2012, 29(9):730-741. Xing Y C, Li N, Zhou D, et al. Sesquiterpene coumarins from Ferula sinkiangensis act as neuroinflammation inhibitors[J]. Planta Med, 2017, 83(1/2):135-142. Teng L, Ma G Z, Li L, et al. Karatavicinol a, a new anti-ulcer sesquiterpene coumarin from Ferula sinkiangensis[J]. Chem Nat Compd, 2013, 49(4):606-609. 高源, 邢亚超, 郭俐含, 等. 新疆阿魏树脂不同极性部位对人肺癌细胞的体外抑制作用研究[J]. 现代药物与临床, 2015, 30(4):366-369. Li G Z, Wang J C, Li X J, et al. An unusual sesquiterpene coumarin from the seeds of Ferula sinkiangensis[J]. J Asian Nat Prod Res, 2016, 18(9):891-896. Ye B G, Wang S, Zhang L. Studies on the detoxification effects and acute toxicity of a mixture of cis-sec-butyl-1-propoenyl disulphide and trans-sec-butyl-1-propoenyl disulphide isolated from crude essential oil of Ferula sinkiangensis K.M. Shen, a Chinese traditional herbal medicine[J]. Nat Prod Res, 2011, 25(12):1161-1170. 王光明, 朝梁, 宋亚伟, 等. 砂茴香化学成分研究[J]. 中国药学杂志, 2024, 59(23):2216-2225. Kang X R, Wu L L, Zhao C L, et al. A new sesquiterpene coumarins from Ferula bungeana Kitagawa[J]. Nat Prod Res, 2025, 39(14):4112-4116. Yang R L, Yan Z H, Lu Y. Cytotoxic phenylpropanoids from carrot[J]. J Agric Food Chem, 2008, 56(9):3024-3027. You C X, Jiang H Y, Zhang W J, et al. Contact toxicity and repellency of the main components from the essential oil of Clausena anisum-olens against two stored product insects[J]. J Insect Sci, 2015, 15(1):87. Babekov A U, Khasanova K I, Eshbakova K A, et al. Chemical constituents of Ferula lapidosa[J]. Chem Nat Compd, 2024, 60(1):177-179. Iranshahi M, Hosseini S T, Sahebkar A H, et al. Diversivittatin, a new phenylpropanoid derivative from the roots of Ferula diversivittata[J]. Chem Nat Compd, 2010, 46(2):192-194. Zhang M M, Kamoldinov K S, Kodirova D R, et al. Chemical constituents from Ferula samarkandica[J]. Chem Nat Compd, 2024, 60(2):367-370. Sreedhar E, Sateesh Chandra Kumar R, Venkateswar Reddy G, et al. The first total synthesis of neohelmanticins A-D, amino derivatives of the 1, 2-dihydroxypropane core and biological evaluation[J]. Tetrahedron Asymmetry, 2009, 20(4):440-448. Sreedhar E, Sateesh Chandra Kumar R, Venkateswar Reddy G, et al. The first total synthesis of neohelmanticins A-D, amino derivatives of the 1, 2-dihydroxypropane core and biological evaluation[J]. Tetrahedron Asymmetry, 2009, 20(4):440-448. Xue G M, Xue J F, Zhao C G, et al. Sesquiterpenoids from Artemisia argyi and their NO production inhibitory activity in RAW264.7 cells[J]. Nat Prod Res, 2021, 35(17):2887-2894. 贾瑶瑶, 冯好, 刘艺, 等. 黑风藤中一个新的降桉叶烷型倍半萜[J]. 药学学报, 2025, 60(9):2858-2862.
2026年第57卷第8期
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doi: 10.7501/j.issn.0253-2670.2026.08.013
接收时间:2026-02-18
首发时间:2026-09-09
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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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