Article(id=1304388245295489857, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388135723496407, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.13.003, 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=1788919992040, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788919992040, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788919992040, creator=13701087609, updateTime=1788919992040, 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=4969, endPage=4978, ext={EN=ArticleExt(id=1304388245714920259, articleId=1304388245295489857, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Chemical constituents of Euphorbia heterophylla and their antioxidant activity, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To study the chemical constituents and in vitro antioxidant activity of Euphorbia heterophylla . Methods Comprehensive separation and purification were performed using normal-phase silica gel column chromatography, Sephadex LH-20 gel column chromatography and semi-preparative HPLC. Their structures were elucidated by comprehensive spectroscopic analyses (1D NMR, 2D NMR, HRMS) combined with single-crystal X-ray diffraction. The in vitro antioxidant activities of the isolated compounds were evaluated by DPPH and ABTS methods. Results A total of 18 compounds were isolated from the ethanol extract of E. heterophylla , their structures were elucidated as (3R ,5R ,8R ,9R ,13S ,14R ,17R ,18R ,21R )-3-hydroxy-21-isopropyl-4,4,9,13,14,17-hexamethyl-cyclopenta[a]chrysen-1(10)-en-2-one (1 ), β-amyrin ferulate (2 ), stigmasterol-4-en-3-one (3 ), isoquercitrin (4 ), quercetin 3-O -α-L -rhamnoside (5 ), kaempferol-3-O -α-arabifuranoside (6 ), kaempferol-3-O -α-L -rhamnoside (7 ), multiflorin A (8 ), 4,6-dimethoxyphthalide (9 ), vanillin (10 ), p -hydroxybenzaldehyde (11 ), protocatechuic acid (12 ), vanillic acid (13 ), 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl) propan-1-one (14 ), ferulic acid (15 ), diethylhexyl adipate (16 ), 13-propylheptacosane (17 ) and 1-n -decanoyl hydroxy-benzoic acid (18 ), respectively. Antioxidant activity evaluation revealed that compounds 5 and 15 exhibited potent DPPH radical scavenging activity, with half maximal inhibitory concentration (IC50 ) values of (15.88 ± 0.84) μg/mL and (15.95 ± 0.75) μg/mL, respectively. Moreover, compound 15 also exhibited potent ABTS radical scavenging activity, with an IC50 value of (2.54 ± 0.57) μg/mL, outperforming the positive control L -ascorbic acid [(IC50 12.25 ± 0.82) μg/mL]. Conclusion Compound 1 is a novel fernane-type triterpenoid and named as euheterophyllfernane A, compounds 2 —3 , 6 —11 , 14 and 16 —18 are isolated from E. heterophylla for the first time., authors=WU Guonan, YUAN Zhenyi, ZOU Kun, WANG Lei, LIU Chengxiong, authorsList=WU Guonan, YUAN Zhenyi, ZOU Kun, WANG Lei, LIU Chengxiong, 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=1304388245534565186, articleId=1304388245295489857, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=白苞猩猩草化学成分及其抗氧化活性, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究白苞猩猩草Euphorbia heterophylla 的化学成分及其体外抗氧化活性。方法 综合运用正、反相硅胶柱色谱、Sephadex LH-20凝胶柱色谱和半制备HPLC等色谱技术对化合物进行分离纯化,并用现代波谱技术(1D NMR、2D NMR、HRMS)及单晶X射线衍射等方法进行化合物的结构鉴定。采用2,2-联苯基-1-苦基肼基(2,2-diphenyl-1-picrylhydrazyl,DPPH)和 2,2-联氮二(3-乙基-苯并噻唑-6-磺酸)二铵盐[2,2'-azinobis-(3-ethylbenzthiazoline-6-sulphonate),ABTS] 法评价单体化合物的体外抗氧化活性。结果 从白苞猩猩草乙醇提取物中分离得到18个化合物,分别鉴定为 (3R ,5R ,8R ,9R ,13S ,14R ,17R , 18R ,21R )-3-羟基-21-异丙基-4,4,9,13,14,17-6甲基-环戊并[a]䓛-1(10)-双键-2-酮(1 )、β-amyrin ferulate(2 )、豆甾-4-烯-3-酮(3 )、异槲皮苷(4 )、槲皮素3-O -α-L -鼠李糖苷(5 )、山柰酚-3-O -α-L 呋喃阿拉伯糖苷(6 )、山柰酚-3-O -α-L -鼠李糖苷(7 )、multiflorin A(8 )、4,6-二甲氧基苯酞(9 )、香草醛(10 )、对羟基苯甲醛(11 )、原儿茶酸(12 )、香草酸(13 )、3-hydroxy-1-(4-hydroxy-3-methoxyphenyl) propan-1-one(14 )、阿魏酸(15 )、己二酸二乙基己酯(16 )、13-丙基-二十五烷(17 )和1-壬酰基羟基苯甲酸(18 )。抗氧化活性研究结果表明,化合物5 和15 对DPPH自由基显示较好的抑制作用,半数抑制浓度(half maximal inhibitory concentration,IC₅₀)值分别为(15.88±0.84)μg/mL和(15.95±0.75)μg/mL。化合物15 对ABTS自由基显示明显的抑制作用,其IC₅₀值为(2.54±0.57)μg/mL,优于阳性药L -抗坏血酸 [IC₅₀为(12.25±0.82)μg/mL]。结论 化合物1 为新的羊齿烷型三萜,命名为白苞羊齿三萜A;化合物2 ~3 、6 ~11 、14 、16 ~18 均为首次从该植物中分离得到。, authors=吴国楠1 , 袁祯熠2 , 邹坤1,2 , 汪蕾1,2 , 刘呈雄2 , authorsList=吴国楠, 袁祯熠, 邹坤, 汪蕾, 刘呈雄, authorCompany=1 三峡大学健康医学院现代药物制剂宜昌市重点实验室, 湖北 宜昌 443002; 2 三峡大学生物与制药学院天然产物研究与利用湖北省重点实验室, 湖北 宜昌 443002, correspAuthors=汪蕾, authorNote=吴国楠: 吴国楠(2001—),女,硕士研究生,研究方向为天然产物化学。E-mail:2912443610@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=UOIzefxc+SSzb/4JYh641w==, pdfFileSize=998507, 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=湖北省中央引导地方科技发展资金项目 (2024BSB016); 三峡大学人才科研启动基金项目 (8253302))}, authors=[Author(id=1307463351588647492, tenantId=1146029695717560320, journalId=null, 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中草药
|化学成分
2026
, 57
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4969
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白苞猩猩草化学成分及其抗氧化活性
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吴国楠, 袁祯熠, 邹坤, 汪蕾, 刘呈雄
作者信息
通讯作者:
汪蕾
作者简介:
吴国楠: 吴国楠(2001—),女,硕士研究生,研究方向为天然产物化学。E-mail:2912443610@qq.com
Chemical constituents of Euphorbia heterophylla and their antioxidant activity
WU Guonan, YUAN Zhenyi, ZOU Kun, WANG Lei, LIU Chengxiong
Affiliations
doi: 10.7501/j.issn.0253-2670.2026.13.003
文章导航
目的 研究白苞猩猩草Euphorbia heterophylla 的化学成分及其体外抗氧化活性。方法 综合运用正、反相硅胶柱色谱、Sephadex LH-20凝胶柱色谱和半制备HPLC等色谱技术对化合物进行分离纯化,并用现代波谱技术(1D NMR、2D NMR、HRMS)及单晶X射线衍射等方法进行化合物的结构鉴定。采用2,2-联苯基-1-苦基肼基(2,2-diphenyl-1-picrylhydrazyl,DPPH)和 2,2-联氮二(3-乙基-苯并噻唑-6-磺酸)二铵盐[2,2'-azinobis-(3-ethylbenzthiazoline-6-sulphonate),ABTS] 法评价单体化合物的体外抗氧化活性。结果 从白苞猩猩草乙醇提取物中分离得到18个化合物,分别鉴定为 (3R ,5R ,8R ,9R ,13S ,14R ,17R , 18R ,21R )-3-羟基-21-异丙基-4,4,9,13,14,17-6甲基-环戊并[a]䓛-1(10)-双键-2-酮(1 )、β-amyrin ferulate(2 )、豆甾-4-烯-3-酮(3 )、异槲皮苷(4 )、槲皮素3-O -α-L -鼠李糖苷(5 )、山柰酚-3-O -α-L 呋喃阿拉伯糖苷(6 )、山柰酚-3-O -α-L -鼠李糖苷(7 )、multiflorin A(8 )、4,6-二甲氧基苯酞(9 )、香草醛(10 )、对羟基苯甲醛(11 )、原儿茶酸(12 )、香草酸(13 )、3-hydroxy-1-(4-hydroxy-3-methoxyphenyl) propan-1-one(14 )、阿魏酸(15 )、己二酸二乙基己酯(16 )、13-丙基-二十五烷(17 )和1-壬酰基羟基苯甲酸(18 )。抗氧化活性研究结果表明,化合物5 和15 对DPPH自由基显示较好的抑制作用,半数抑制浓度(half maximal inhibitory concentration,IC₅₀)值分别为(15.88±0.84)μg/mL和(15.95±0.75)μg/mL。化合物15 对ABTS自由基显示明显的抑制作用,其IC₅₀值为(2.54±0.57)μg/mL,优于阳性药L -抗坏血酸 [IC₅₀为(12.25±0.82)μg/mL]。结论 化合物1 为新的羊齿烷型三萜,命名为白苞羊齿三萜A;化合物2 ~3 、6 ~11 、14 、16 ~18 均为首次从该植物中分离得到。
白苞猩猩草
/
羊齿烷型三萜
/
抗氧化活性
/
白苞羊齿三萜A
/
槲皮素3-O -α-L -鼠李糖苷
/
阿魏酸
Objective To study the chemical constituents and in vitro antioxidant activity of Euphorbia heterophylla . Methods Comprehensive separation and purification were performed using normal-phase silica gel column chromatography, Sephadex LH-20 gel column chromatography and semi-preparative HPLC. Their structures were elucidated by comprehensive spectroscopic analyses (1D NMR, 2D NMR, HRMS) combined with single-crystal X-ray diffraction. The in vitro antioxidant activities of the isolated compounds were evaluated by DPPH and ABTS methods. Results A total of 18 compounds were isolated from the ethanol extract of E. heterophylla , their structures were elucidated as (3R ,5R ,8R ,9R ,13S ,14R ,17R ,18R ,21R )-3-hydroxy-21-isopropyl-4,4,9,13,14,17-hexamethyl-cyclopenta[a]chrysen-1(10)-en-2-one (1 ), β-amyrin ferulate (2 ), stigmasterol-4-en-3-one (3 ), isoquercitrin (4 ), quercetin 3-O -α-L -rhamnoside (5 ), kaempferol-3-O -α-arabifuranoside (6 ), kaempferol-3-O -α-L -rhamnoside (7 ), multiflorin A (8 ), 4,6-dimethoxyphthalide (9 ), vanillin (10 ), p -hydroxybenzaldehyde (11 ), protocatechuic acid (12 ), vanillic acid (13 ), 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl) propan-1-one (14 ), ferulic acid (15 ), diethylhexyl adipate (16 ), 13-propylheptacosane (17 ) and 1-n -decanoyl hydroxy-benzoic acid (18 ), respectively. Antioxidant activity evaluation revealed that compounds 5 and 15 exhibited potent DPPH radical scavenging activity, with half maximal inhibitory concentration (IC50 ) values of (15.88 ± 0.84) μg/mL and (15.95 ± 0.75) μg/mL, respectively. Moreover, compound 15 also exhibited potent ABTS radical scavenging activity, with an IC50 value of (2.54 ± 0.57) μg/mL, outperforming the positive control L -ascorbic acid [(IC50 12.25 ± 0.82) μg/mL]. Conclusion Compound 1 is a novel fernane-type triterpenoid and named as euheterophyllfernane A, compounds 2 —3 , 6 —11 , 14 and 16 —18 are isolated from E. heterophylla for the first time.
Euphorbia heterophylla L.
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fernane-type triterpenoids
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antioxidant activity
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euheterophyllfernane A
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quercetin 3-O -α-L -rhamnoside
/
ferulic acid
吴国楠, 袁祯熠, 邹坤, 汪蕾, 刘呈雄.
白苞猩猩草化学成分及其抗氧化活性.
中草药,
2026
, 57
(13)
: 4969
-4978
.
DOI: 10.7501/j.issn.0253-2670.2026.13.003
WU Guonan, YUAN Zhenyi, ZOU Kun, WANG Lei, LIU Chengxiong.
Chemical constituents of Euphorbia heterophylla and their antioxidant activity[J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(13)
: 4969
-4978
.
DOI: 10.7501/j.issn.0253-2670.2026.13.003
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2026年第57卷第13期
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doi: 10.7501/j.issn.0253-2670.2026.13.003
接收时间:2026-04-07
首发时间:2026-09-09
https://castjournals.cast.org.cn/joweb/zcy/CN/10.7501/j.issn.0253-2670.2026.13.003
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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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