Article(id=1322631196262118189, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631195876242221, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.17.002, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1781020800000, receivedDateStr=2026-06-10, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793269450488, onlineDateStr=2026-10-29, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793269450488, onlineIssueDateStr=2026-10-29, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793269450488, creator=13701087609, updateTime=1793269450488, 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=6669, endPage=6676, ext={EN=ArticleExt(id=1322631196618634031, articleId=1322631196262118189, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=A new isoflavone compound isolated from Dalbergia pinnata, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical composition of the rhizome of Dalbergia pinnata. Methods Separation and purification were performed using silica gel, RP-C18, MCI, Sephadex LH-20 column chromatography, semi-preparative high-performance liquid chromatography and recrystallization; compound structures were identified based on spectroscopic techniques, including NMR spectroscopy; and the anti-complement activity of selected isolated monomeric compounds was screened using an in vitro erythrocyte hemolysis assay. Results Fifteen compounds were isolated and identified from the ethyl acetate fraction of D. pinnata, including 5,7,4′-trihydroxy-6,2′,5′-trimethoxyisoflavone (1), 7,3 ¢-dihydroxy-8,4 ¢-dimethoxyisoflavone (2), (&8722;)-vestitol (3), 3-O-acetyloleanolic acid (4), (&8722;)-hydroxymedioresinol (5), (&8722;)-episyringaresinol (6), (&8722;)-liquiritigenin (7), butein (8), (&8722;)- isolariciresinol (9), (+)-lyoniresinol (10), (2R)-3-(3 ¢,4¢-dimethoxyphenyl)-1,2-propanediol (11), (2R)-3-(3 ¢,4 ¢,5 ¢-trimethoxyphenyl)-1,2-propanediol (12), 3,3 ¢,4,4 ¢-tetrahydroxybiphenyl (13), vanillicvanillyric acid (14), cinnamtannin B1 (15). In vitro anti-complement activity assays demonstrated that compounds 1, 3, 7 and 8 exhibited distinct in vitro complement inhibitory activities, with their half-maximal hemolysis-inhibitory concentrations (CH50) measuring (1.21 ± 0.07), (0.57 ± 0.03), (0.12 ± 0.13) and (0.17 ± 0.04) mg/mL respectively. Conclusion Compound 1 is a new compound, designated as dalbergiaisoflavone A, obtained from D. pinnata; compounds 2—6 and 8—15 were obtained from this species for the first time, and compound 7 exhibits significant in vitro anti-complement activity., authors=XIONG Yalan1, ZHU Min1, LIAO Tuhua1, LU Chengsheng2,3, HUANG Sulin1, WANG Guangxian1, WEI Jianhua1,2,3, LIANG Chenyan1,3, FENG Xu1,3, authorsList=XIONG Yalan, ZHU Min, LIAO Tuhua, LU Chengsheng, HUANG Sulin, WANG Guangxian, WEI Jianhua, LIANG Chenyan, FENG Xu, authorCompany=1 School of Pharmacy, Guangxi University of Chinese Medicine, Nanning 530200, China;
2 Teaching Center of Experiment and Practical Training, Guangxi University of Chinese Medicine, Nanning 530200, China;
3 National Demonstration Center for Experimental Chinese Medicine Education, Guangxi University of Chinese Medicine, Nanning 530200, 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=1322631196538942254, articleId=1322631196262118189, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=斜叶黄檀中1个新的异黄酮类化合物, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究斜叶黄檀Dalbergia pinnata 根茎的化学成分。方法 利用硅胶、RP-C₁₈、MCI、Sephadex LH-20柱色谱、半制备型高效液相色谱及重结晶等方法进行分离纯化,通过核磁共振等波谱技术确定化合物的结构;采用体外红细胞溶血法对分离得到的部分单体化合物进行抗补体活性筛选。结果 从斜叶黄檀醋酸乙酯部位中分离鉴定了15个化合物,分别为5,7,4′-三羟基-6,2′,5′-三甲氧基异黄酮(1)、7,3¢-二羟基-8,4¢-二甲氧基异黄酮(2)、(-)-驴食草酚(3)、3-O-乙酰基齐墩果酸(4)、(-)-杜仲树脂酚(5)、(-)-表丁香脂素(6)、(-)-甘草素(7)、紫铆因(8)、(-)-异落叶松脂素(9)、(+)-南烛木树脂酚(10)、(2R)-3-(3¢,4¢-二甲氧基苯基)-1,2-丙二醇(11)、(2R)-3-(3¢,4¢,5¢-三甲氧基苯基)-1,2-丙二醇(12)、3,3¢,4,4¢-四羟基联苯(13)、香草酸(14)、桂皮鞣质B1(15)。体外抗补体活性结果表明,化合物1、3、7、8具有不同的体外补体抑制活性,其半数抑制溶血浓度(50% hemolytic complement activity,CH₅₀)分别为(1.21±0.07)、(0.57±0.03)、(0.12±0.13)、(0.17±0.04)mg/mL。结论 化合物1为新化合物,命名为斜叶异黄酮A,化合物2~6、8~15为首次从该植物中分离得到,化合物7具有显著的体外抗补体活性。, authors=熊亚兰1, 朱敏1, 廖土花1, 卢澄生2,3, 黄嫊琳1, 王广贤1, 韦建华1,2,3, 梁臣艳1,3, 冯旭1,3, authorsList=熊亚兰, 朱敏, 廖土花, 卢澄生, 黄嫊琳, 王广贤, 韦建华, 梁臣艳, 冯旭, authorCompany=1 广西中医药大学药学院, 广西南宁 530200;
2 广西中医药大学 教学实验实训中心, 广西 南宁 530200;
3 广西中医药大学中药学国家级实验教学示范中心, 广西 南宁 530200, correspAuthors=梁臣艳, authorNote=熊亚兰: 熊亚兰(2001—),女,硕士研究生,研究方向为中药化学。E-mail:2408266811@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=ogv0K10QPHloFTcTfc7G3A==, pdfFileSize=1204429, 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=广西自然科学基金项目 (2024GXNSFAA010266); 广西自然科学基金项目 (2024GXNSFAA010326); 广西特色中药现代化产业学院2024年大学生创新创业训练计划立项项目 (C202409); 广西中医药大学自然科学基金项目 (2022MS031))}, authors=null, keywords=[Keyword(id=1322634592297800079, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631196262118189, language=CN, orderNo=1, keyword=斜叶黄檀), Keyword(id=1322634592390074768, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631196262118189, language=CN, orderNo=2, keyword=斜叶异黄酮A), Keyword(id=1322634592465572241, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631196262118189, language=CN, orderNo=3, keyword=7,3 ¢), Keyword(id=1322634592549458322, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631196262118189, language=CN, orderNo=4, keyword=-二羟基-8,4 ¢), Keyword(id=1322634592633344403, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631196262118189, language=CN, orderNo=5, keyword=-二甲氧基异黄酮), Keyword(id=1322634592692064660, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631196262118189, language=CN, orderNo=6, keyword=(-)-甘草素), Keyword(id=1322634592788533653, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631196262118189, language=CN, orderNo=7, keyword=(-)-异落叶松脂素), Keyword(id=1322634592868225430, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631196262118189, language=CN, orderNo=8, keyword=抗补体活性), Keyword(id=1322634593048580503, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1322631196262118189, language=EN, orderNo=1, keyword=Dalbergia pinnata (Lour.) 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pdfUrlEn=https://castjournals.cast.org.cn/joweb/zcy/EN/PDF/10.7501/j.issn.0253-2670.2026.17.002, aliStartDate=null, aliEndDate=null, collectionFlag=false, citedCount=null, citedUrl=null, previewStatus=0, delFlag=0, hasFullText=0, orderTime=1789142400000, fullTextJson=null, articleText=null, reference=黄燮才. 广西民族药简编[M]. 南宁: 广西壮族自治区卫生局药品检验所, 1980: 126.
中国科学院中国植物志编辑委员会. 中国植物志(第四十卷) [M]. 北京: 科学出版社, 1994: 112-113.
国家中医药管理局《中华本草》编委会. 中华本草(第4卷) [M]. 上海: 科学技术出版社, 1999: 3107.
何欢, 王维玉, 朱敏, 等. 壮药斜叶黄檀中黄酮类成分研究[J]. 中药材, 2023, 46(1): 106-110.
覃川娴, 丘君凤, 黄清霞, 等. 斜叶黄檀薄层鉴别方法的建立[J]. 壮瑶药研究, 2023(3): 92-96.
李浩杰. 斜叶黄檀结香木的识别特征及等级划分[D]. 雅安: 四川农业大学, 2023.
梁居红, 杜丽敏, 麦有专, 等. 海南霸王岭的斜叶檀野生资源调查[J]. 热带林业, 2015, 43(3): 34-35.
苏妙铃, 杨健妮, 周秀悄, 等. 斜叶黄檀心材精油成分的GC-MS分析[J]. 广东化工, 2020, 47(5): 14-17.
鲁轮, 赵维波, 于兵兵, 等. 不同产地斜叶檀挥发油成分的比较分析研究[J]. 中国现代应用药学, 2021, 38(3): 299-304.
张姣, 德吉, 付爱玲, 等. 密枝圆柏的化学成分及其抗补体、抗氧化活性[J]. 中草药, 2019, 50(13): 3008-3016.
张贵杰, 李宁, 熊元君, 等. 骆驼刺的化学成分研究[J]. 中国药学杂志, 2009, 44(12): 897-899.
Zhao X B, Mei W L, Gong M F, et al. Antibacterial activity of the flavonoids from Dalbergia odorifera on Ralstonia solanacearum [J]. Molecules, 2011, 16(12): 9775-9782.
李江, 李䶮, 穆淑珍, 等. 黔产昆明山海棠化学成分及其抑菌活性研究[J]. 广西植物, 2019, 39(11): 1505-1511.
李汉芬, 秦诗慧, 周泽琴, 等. 大苞鞘石斛酚类化学成分研究[J]. 中草药, 2024, 55(3): 711-719.
徐志贫, 王彦志, 郭燕, 等. 牛膝地上部位化学成分的分离鉴定[J]. 国际药学研究杂志, 2020, 47(6): 450-455.
缪丽兰, 陈孝礼, 江文婧, 等. 刺槐根化学成分的研究[J]. 中成药, 2023, 45(9): 2929-2933.
姜李红, 张胜男, 龚桂芬, 等. 鬼针草化学成分及α-葡萄糖苷酶抑制活性研究[J]. 中南药学, 2022, 20(12): 2740-2746.
曾发古, 苏倩. 油茶果壳乙酸乙酯部位化学成分的研究[J]. 山东化工, 2023, 52(23): 55-57.
曾雨娴, 廖广凤, 李金玲, 等. 毛草龙化学成分及其细胞毒活性研究[J]. 广西植物, 2024, 44(6): 1195-1204.
Ban N K, Truong L H, Linh T M, et al. Phenolic compounds from Trigonostemon honbaensis and their cytotoxic activity [J]. Vietnam J Chem, 2020, 58(6): 759-764.
潘兰, 贾新岳, 贾晓光, 等. 狭叶锦鸡儿根化学成分研究[J]. 国际药学研究杂志, 2020, 47(12): 1152-1157.
刘健, 肖朝江, 崔淑君, 等. 匙萼金丝桃化学成分及镇痛与抗疟活性研究[J]. 中国药学杂志, 2019, 54(8): 614-619.
杜伟东, 吴蓓, 李志峰, 等. 小花清风藤化学成分的分离与鉴定(II) [J]. 中草药, 2019, 50(18): 4277-4280.
张朝凤. 乌药与鼎湖钓樟的化学成分及抗HIV-1整合酶活性研究[D]. 沈阳: 沈阳药科大学, 2002.)
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斜叶黄檀中1个新的异黄酮类化合物
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中草药 | 化学成分 2026,57(17): 6669-6676
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中草药 |化学成分 2026 , 57 (17) : 6669 -6676
斜叶黄檀中1个新的异黄酮类化合物
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熊亚兰1, 朱敏1, 廖土花1, 卢澄生2,3, 黄嫊琳1, 王广贤1, 韦建华1,2,3, 梁臣艳1,3, 冯旭1,3
作者信息
    1 广西中医药大学药学院, 广西南宁 530200;
    2 广西中医药大学 教学实验实训中心, 广西 南宁 530200;
    3 广西中医药大学中药学国家级实验教学示范中心, 广西 南宁 530200
通讯作者:
梁臣艳
作者简介:
熊亚兰: 熊亚兰(2001—),女,硕士研究生,研究方向为中药化学。E-mail:2408266811@qq.com
A new isoflavone compound isolated from Dalbergia pinnata
  • XIONG Yalan1, ZHU Min1, LIAO Tuhua1, LU Chengsheng2,3, HUANG Sulin1, WANG Guangxian1, WEI Jianhua1,2,3, LIANG Chenyan1,3, FENG Xu1,3
  • Affiliations
      1 School of Pharmacy, Guangxi University of Chinese Medicine, Nanning 530200, China;
      2 Teaching Center of Experiment and Practical Training, Guangxi University of Chinese Medicine, Nanning 530200, China;
      3 National Demonstration Center for Experimental Chinese Medicine Education, Guangxi University of Chinese Medicine, Nanning 530200, China
    doi: 10.7501/j.issn.0253-2670.2026.17.002
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    目的 研究斜叶黄檀Dalbergia pinnata 根茎的化学成分。方法 利用硅胶、RP-C₁₈、MCI、Sephadex LH-20柱色谱、半制备型高效液相色谱及重结晶等方法进行分离纯化,通过核磁共振等波谱技术确定化合物的结构;采用体外红细胞溶血法对分离得到的部分单体化合物进行抗补体活性筛选。结果 从斜叶黄檀醋酸乙酯部位中分离鉴定了15个化合物,分别为5,7,4′-三羟基-6,2′,5′-三甲氧基异黄酮(1)、7,3¢-二羟基-8,4¢-二甲氧基异黄酮(2)、(-)-驴食草酚(3)、3-O-乙酰基齐墩果酸(4)、(-)-杜仲树脂酚(5)、(-)-表丁香脂素(6)、(-)-甘草素(7)、紫铆因(8)、(-)-异落叶松脂素(9)、(+)-南烛木树脂酚(10)、(2R)-3-(3¢,4¢-二甲氧基苯基)-1,2-丙二醇(11)、(2R)-3-(3¢,4¢,5¢-三甲氧基苯基)-1,2-丙二醇(12)、3,3¢,4,4¢-四羟基联苯(13)、香草酸(14)、桂皮鞣质B1(15)。体外抗补体活性结果表明,化合物1、3、7、8具有不同的体外补体抑制活性,其半数抑制溶血浓度(50% hemolytic complement activity,CH₅₀)分别为(1.21±0.07)、(0.57±0.03)、(0.12±0.13)、(0.17±0.04)mg/mL。结论 化合物1为新化合物,命名为斜叶异黄酮A,化合物2~6、8~15为首次从该植物中分离得到,化合物7具有显著的体外抗补体活性。
    斜叶黄檀  /  斜叶异黄酮A  /  7,3 ¢  /  -二羟基-8,4 ¢  /  -二甲氧基异黄酮  /  (-)-甘草素  /  (-)-异落叶松脂素  /  抗补体活性
    Objective To investigate the chemical composition of the rhizome of Dalbergia pinnata. Methods Separation and purification were performed using silica gel, RP-C18, MCI, Sephadex LH-20 column chromatography, semi-preparative high-performance liquid chromatography and recrystallization; compound structures were identified based on spectroscopic techniques, including NMR spectroscopy; and the anti-complement activity of selected isolated monomeric compounds was screened using an in vitro erythrocyte hemolysis assay. Results Fifteen compounds were isolated and identified from the ethyl acetate fraction of D. pinnata, including 5,7,4′-trihydroxy-6,2′,5′-trimethoxyisoflavone (1), 7,3 ¢-dihydroxy-8,4 ¢-dimethoxyisoflavone (2), (&8722;)-vestitol (3), 3-O-acetyloleanolic acid (4), (&8722;)-hydroxymedioresinol (5), (&8722;)-episyringaresinol (6), (&8722;)-liquiritigenin (7), butein (8), (&8722;)- isolariciresinol (9), (+)-lyoniresinol (10), (2R)-3-(3 ¢,4¢-dimethoxyphenyl)-1,2-propanediol (11), (2R)-3-(3 ¢,4 ¢,5 ¢-trimethoxyphenyl)-1,2-propanediol (12), 3,3 ¢,4,4 ¢-tetrahydroxybiphenyl (13), vanillicvanillyric acid (14), cinnamtannin B1 (15). In vitro anti-complement activity assays demonstrated that compounds 1, 3, 7 and 8 exhibited distinct in vitro complement inhibitory activities, with their half-maximal hemolysis-inhibitory concentrations (CH50) measuring (1.21 ± 0.07), (0.57 ± 0.03), (0.12 ± 0.13) and (0.17 ± 0.04) mg/mL respectively. Conclusion Compound 1 is a new compound, designated as dalbergiaisoflavone A, obtained from D. pinnata; compounds 2—6 and 8—15 were obtained from this species for the first time, and compound 7 exhibits significant in vitro anti-complement activity.
    Dalbergia pinnata (Lour.) Prain  /  dalbergiaisoflavone A  /  3 ¢  /  ,7-dihydroxy-8,4 ¢  /  -dimethoxyisoflavone  /  (-)-liquiritigenin  /  (-)-isolariciresinol  /  anti-complement activity
    熊亚兰, 朱敏, 廖土花, 卢澄生, 黄嫊琳, 王广贤, 韦建华, 梁臣艳, 冯旭. 斜叶黄檀中1个新的异黄酮类化合物. 中草药, 2026 , 57 (17) : 6669 -6676 . DOI: 10.7501/j.issn.0253-2670.2026.17.002
    XIONG Yalan, ZHU Min, LIAO Tuhua, LU Chengsheng, HUANG Sulin, WANG Guangxian, WEI Jianhua, LIANG Chenyan, FENG Xu. A new isoflavone compound isolated from Dalbergia pinnata[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (17) : 6669 -6676 . DOI: 10.7501/j.issn.0253-2670.2026.17.002

      广西自然科学基金项目 (2024GXNSFAA010266); 广西自然科学基金项目 (2024GXNSFAA010326); 广西特色中药现代化产业学院2024年大学生创新创业训练计划立项项目 (C202409); 广西中医药大学自然科学基金项目 (2022MS031)

    参考文献 引证文献
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    黄燮才. 广西民族药简编[M]. 南宁: 广西壮族自治区卫生局药品检验所, 1980: 126.
    中国科学院中国植物志编辑委员会. 中国植物志(第四十卷) [M]. 北京: 科学出版社, 1994: 112-113.
    国家中医药管理局《中华本草》编委会. 中华本草(第4卷) [M]. 上海: 科学技术出版社, 1999: 3107.
    何欢, 王维玉, 朱敏, 等. 壮药斜叶黄檀中黄酮类成分研究[J]. 中药材, 2023, 46(1): 106-110.
    覃川娴, 丘君凤, 黄清霞, 等. 斜叶黄檀薄层鉴别方法的建立[J]. 壮瑶药研究, 2023(3): 92-96.
    李浩杰. 斜叶黄檀结香木的识别特征及等级划分[D]. 雅安: 四川农业大学, 2023.
    梁居红, 杜丽敏, 麦有专, 等. 海南霸王岭的斜叶檀野生资源调查[J]. 热带林业, 2015, 43(3): 34-35.
    苏妙铃, 杨健妮, 周秀悄, 等. 斜叶黄檀心材精油成分的GC-MS分析[J]. 广东化工, 2020, 47(5): 14-17.
    鲁轮, 赵维波, 于兵兵, 等. 不同产地斜叶檀挥发油成分的比较分析研究[J]. 中国现代应用药学, 2021, 38(3): 299-304.
    张姣, 德吉, 付爱玲, 等. 密枝圆柏的化学成分及其抗补体、抗氧化活性[J]. 中草药, 2019, 50(13): 3008-3016.
    张贵杰, 李宁, 熊元君, 等. 骆驼刺的化学成分研究[J]. 中国药学杂志, 2009, 44(12): 897-899.
    Zhao X B, Mei W L, Gong M F, et al. Antibacterial activity of the flavonoids from Dalbergia odorifera on Ralstonia solanacearum [J]. Molecules, 2011, 16(12): 9775-9782.
    李江, 李䶮, 穆淑珍, 等. 黔产昆明山海棠化学成分及其抑菌活性研究[J]. 广西植物, 2019, 39(11): 1505-1511.
    李汉芬, 秦诗慧, 周泽琴, 等. 大苞鞘石斛酚类化学成分研究[J]. 中草药, 2024, 55(3): 711-719.
    徐志贫, 王彦志, 郭燕, 等. 牛膝地上部位化学成分的分离鉴定[J]. 国际药学研究杂志, 2020, 47(6): 450-455.
    缪丽兰, 陈孝礼, 江文婧, 等. 刺槐根化学成分的研究[J]. 中成药, 2023, 45(9): 2929-2933.
    姜李红, 张胜男, 龚桂芬, 等. 鬼针草化学成分及α-葡萄糖苷酶抑制活性研究[J]. 中南药学, 2022, 20(12): 2740-2746.
    曾发古, 苏倩. 油茶果壳乙酸乙酯部位化学成分的研究[J]. 山东化工, 2023, 52(23): 55-57.
    曾雨娴, 廖广凤, 李金玲, 等. 毛草龙化学成分及其细胞毒活性研究[J]. 广西植物, 2024, 44(6): 1195-1204.
    Ban N K, Truong L H, Linh T M, et al. Phenolic compounds from Trigonostemon honbaensis and their cytotoxic activity [J]. Vietnam J Chem, 2020, 58(6): 759-764.
    潘兰, 贾新岳, 贾晓光, 等. 狭叶锦鸡儿根化学成分研究[J]. 国际药学研究杂志, 2020, 47(12): 1152-1157.
    刘健, 肖朝江, 崔淑君, 等. 匙萼金丝桃化学成分及镇痛与抗疟活性研究[J]. 中国药学杂志, 2019, 54(8): 614-619.
    杜伟东, 吴蓓, 李志峰, 等. 小花清风藤化学成分的分离与鉴定(II) [J]. 中草药, 2019, 50(18): 4277-4280.
    张朝凤. 乌药与鼎湖钓樟的化学成分及抗HIV-1整合酶活性研究[D]. 沈阳: 沈阳药科大学, 2002.
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