Article(id=1304415005823226298, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414997581427653, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.08.011, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1771948800000, receivedDateStr=2026-02-25, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788926372246, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788926372246, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788926372246, creator=13701087609, updateTime=1788926372246, 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=2981, endPage=2988, ext={EN=ArticleExt(id=1304415006141993404, articleId=1304415005823226298, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=A new E-ring cleavage spirostan isolated from Hosta plantaginea flower, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical components in the Hosta plantaginea flower and evaluate their anti-inflammatory activities. Method The extraction was carried out using 95% and 70% ethanol aqueous solutions through percolation, followed by liquid-liquid extraction with petroleum ether and ethyl acetate. The chemical components were separated and purified by column chromatography methods such as D101 macroporous adsorption resin, silica gel, and ODS, as well as preparative liquid chromatography. Structural identification was conducted using high-resolution mass spectrometry, nuclear magnetic resonance spectroscopy, and circular dichroism spectrum (ECD). Moreover, the anti-inflammatory activities of all compounds were evaluated. Results Ten compounds were obtained from the aqueous layer of the H. plantaginea flower ethanol extract after extraction with ethyl acetate, including three steroids (1–3), four flavonoids (4–7), two alkaloids (8, 9), and one fatty acid (10). They were identified as (8S,9R,10S, 12S,13R,14R,16R,17S,20R,22S,25R,26R)-12,16-hydroxy-22,26-epoxy-26-methoxy-5α-cholest-4-en-3-one (or hostaspirone A, 1), (2α,3β,5α,25R)-2-hydroxyspirostan-3-yl O-β-D-glucopyranosyl-(1→2)-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (2), (25R)-3-(β-D-Glucopyranosyl-(1→2)-[β-D-xylopyranosyl-(1→3)]-β-D-glucopyranosyl-(1→4)-β-D-galactopyranosyl)-5-spirostan-2α-ol (3), rhamnocitrin-3-O-β-D-glucopyranoside (4), quercetin-3-O-β-glucopyranoside (5), isorhamnetin 3-O-glucoside (6), isorhamnetin-3-O-rutinoside (7), thymine (8), uracil (9), and myristic acid (10), respectively. Conclusion Compound 1 is the first steroid identified in this genus to exhibit an E-ring cleavage spirostan. Compounds 4, 6–8, and 10 were isolated for the first time from the family Asparagaceae, and compound 5 is reported here for the first time from the Hosta genus. In addition, compounds 1 and 4 have some anti-inflammatory effects. This study expands the chemical profile of H. plantaginea and provides a scientific foundation for its potential clinical applications., authors=YUAN Fang, XIA Bowei, YANG Li, LIU Kun, DENG Zitong, ZHANG Shouwen, HE Junwei, authorsList=YUAN Fang, XIA Bowei, YANG Li, LIU Kun, DENG Zitong, ZHANG Shouwen, HE Junwei, 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=1304415006053913019, articleId=1304415005823226298, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=玉簪花中1个新的E环开裂螺甾烷, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究玉簪Hosta plantaginea花中的化学成分及其抗炎活性。方法 采用95%和70%乙醇-水溶液渗漉提取,石油醚和醋酸乙酯萃取,通过D101大孔吸附树脂、硅胶、ODS等柱色谱及制备液相柱色谱等方法进行化学成分的分离与纯化,综合运用高分辨质谱、核磁共振谱、ECD等技术进行结构鉴定,并对所有化合物进行了抗炎活性评价。结果 从玉簪花乙醇提取物经醋酸乙酯萃取后的水层部位中得到了10个化合物,包括3个甾体类(1~3)、4个黄酮类(4~7)、2个生物碱类(8、9)和1个脂肪酸(10);分别鉴定为 (8S,9R,10S,12S,13R,14R,16R,17S,20R,22S,25R,26R)-12,16-二羟基-22,26-环氧-26-甲氧基-5α-胆甾-4-烯-3-酮(1)、(2α,3β,5α,25R)-2-羟基螺甾烷-3-O-β-D-吡喃葡萄糖基-(1→2)-O-β-D-吡喃葡萄糖基-(1→4)-β-D-吡喃半乳糖苷(2)、(25R)-2-羟基螺甾烷-3-β-D-吡喃葡萄糖基-(1→2)-[β-D-吡喃木糖基-(1→3)]-β-D-吡喃葡萄糖基-(1→4)-β-D-吡喃半乳糖苷(3)、鼠李柠檬素-3-O-β-D-葡萄糖苷(4)、槲皮素-3-O-葡萄糖苷(5)、异鼠李素-3-O-葡萄糖苷(6)、异鼠李素-3-O-芸香糖苷(7)、胸腺嘧啶(8)、尿嘧啶(9)和肉豆蔻酸(10)。结论 化合物1为新化合物,命名为玉簪螺甾烷甾体A;化合物4、6~8和10为首次从天门冬科中分离得到,化合物5为首次从玉簪属中分离得到。化合物1和4具有一定的抗炎作用。丰富了玉簪花的化学成分,为其应用提供了一定的科学依据。, authors=袁芳1, 夏博伟1, 杨丽2, 刘坤2, 邓紫童2, 张寿文1, 何军伟1, authorsList=袁芳, 夏博伟, 杨丽, 刘坤, 邓紫童, 张寿文, 何军伟, authorCompany=1 江西中医药大学 中药资源与民族药研究中心, 江西 南昌 330004; 2 江西中医药大学药学院, 江西 南昌 330004, correspAuthors=何军伟, authorNote=袁芳: 袁芳,女,硕士研究生,研究方向为民族药学。E-mail:2406874141@qq.com
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Yang L, He J W. Traditional uses, phytochemistry, pharmacology and toxicological aspects of the genus Hosta (Liliaceae):A comprehensive review[J]. J Ethnopharmacol, 2021, 265:113323. He J W, Wang H L, Li X M, et al. Uncovering the benign prostatic hyperplasia protective mechanism of Hosta plantaginea flower fractions:AMPK/JAK pathways inhibition[J]. J Ethnopharmacol, 2025, 353(Pt B):120362. Li X M, Wang J S, Liang J, et al. Hosta plantaginea flower ameliorates chronic pharyngitis by suppressing inflammation via the JAK-STAT/PI3K/MAPK signaling axis in rats[J]. Chem Biodivers, 2025, 22(7):e202403254. Wang H L, Li X M, Xia B W, et al. Amelioration of chronic prostatitis by fractions of Mongolian medicine Hosta plantaginea flowers via inhibition of NF-κB, MAPKs, JAK-STAT, and PI3K-Akt signaling pathways in rats[J]. J Ethnopharmacol, 2023, 307:116245. Wang J S, Cao L, Wang H L, et al. Therapeutic effect of Hosta plantaginea (Lam.) Aschers flowers on acute pharyngitis through inhibition of multi-inflammatory pathways in rats[J]. J Ethnopharmacol, 2024, 318:116966. Wang H L, Mu Z Q, Liang J, et al. Hosta plantaginea (Lam.) Aschers flower modulates inflammation and amino acid metabolism by inhibiting NF-κB/MAPK/JAK-STAT/PI3K-Akt and AMPK pathways to alleviate benign prostatic hyperplasia in rats[J]. J Ethnopharmacol, 2025, 337:118970. Yang L, Zhang F X, He W W, et al. Extraction optimization and constituent analysis of total flavonoid from Hosta plantaginea (Lam.) Aschers flowers and its ameliorative effect on chronic prostatitis via inhibition of multiple inflammatory pathways in rats[J]. J Ethnopharmacol, 2024, 318:116922. Xia B W, Li X M, Zhang Q C, et al. Revealing the anti-inflammatory mechanism and effective constituents of Hosta plantaginea flowers by a strategy integrating network pharmacology, molecular docking, and experimental verification[J]. Eur J Integr Med, 2024, 71:102400. Yang L, He J W. Hosta plantaginea (Lam.) Aschers (Yuzan):An overview on its botany, traditional use, phytochemistry, quality control and pharmacology[J]. RSC Adv, 2019, 9(60):35050-35058. He J W, Yang L, Mu Z Q, et al. Anti-inflammatory and antioxidant activities of flavonoids from the flowers of Hosta plantaginea[J]. RSC Adv, 2018, 8(32):18175-18179. He J W, Huang X Y, Wang Y Q, et al. A new flavonol glycoside from the flowers of Hosta plantaginea with cyclooxygenases-1/2 inhibitory and antioxidant activities[J]. Nat Prod Res, 2019, 33(11):1599-1604. He J W, Guo P, Yang L, et al. Anti-inflammatory constituents isolated from the flowers of Hosta plantaginea via suppression of the NF-κB signaling pathway in LPS-stimulated RAW 264.7 macrophages[J]. RSC Adv, 2023, 13(11):7179-7184. Fang Y W, Yang L, He J W. Plantanone C attenuates LPS-stimulated inflammation by inhibiting NF-κB/iNOS/COX-2/MAPKs/Akt pathways in RAW 264.7 macrophages[J]. Biomed Pharmacother, 2021, 143:112104. Fang Y W, Wang H L, Xia X Y, et al. Kaempferol 3-O-(2G-glucosylrutinoside)-7-O-glucoside isolated from the flowers of Hosta plantaginea exerts anti-inflammatory activity via suppression of NF-κB, MAPKs and Akt pathways in RAW 264.7 cells[J]. Biomed Pharmacother, 2022, 153:113295. Yang L, Jiang S T, Zhou Q G, et al. Chemical constituents from the flower of Hosta plantaginea with cyclooxygenases inhibition and antioxidant activities and their chemotaxonomic significance[J]. Molecules, 2017, 22(11):1825. Yang L, Lin Y M, He Z W, et al. Hostaflavanol A, a new anti-inflammatory and antioxidant activities flavanol from the flowers of Hosta plantaginea[J]. Med Chem Res, 2020, 29(3):426-430. Yang L, Zhu Y Y, He Z W, et al. Plantanone D, a new rare methyl-flavonoid from the flowers of Hosta plantaginea with anti-inflammatory and antioxidant activities[J]. Nat Prod Res, 2021, 35(22):4331-4337. Yang Y T, Xia B W, Ouyang H, et al. Rapid two-step isolation of kaempferol from the Hosta plantaginea flower and its anti-inflammatory mechanism:Evidence from network pharmacology, molecular docking, molecular dynamics simulation, and experimental validation[J]. Separations, 2025, 12(6):138. Yang L, He J W. Anti-inflammatory effects of flavonoids and phenylethanoid glycosides from Hosta plantaginea flowers in LPS-stimulated RAW 264.7 macrophages through inhibition of the NF-κB signaling pathway[J]. BMC Complementary Med Ther, 2022, 22(1):55. Ksebati M B, Schmitz F J. Minabeolides:A group of withanolides from a soft coral, Minabea sp[J]. J Org Chem, 1988, 53(17):3926-3929. Li C S, Liu L X, Pan W T, et al. Potential chiral fluorescent molecular probes based on an α, β-unsaturated ketone for anion detection[J]. Sci Rep, 2019, 9(1):18838. Liu K Y, Yang J, Tang Y Y, et al. Bioassay-guided isolation of anti-leukemic steroids from Aglaia abbreviata by inducing apoptosis[J]. Bioorg Chem, 2024, 144:107147. Wang Y Q, Bao L, Yang X L, et al. Four new cuparene-type sesquiterpenes from Flammulina velutipes[J]. Helv Chim Acta, 2012, 95(2):261-267. Jiang Y, Wang N L, Yao X S, et al. Steroidal saponins from the bulbs of Allium chinense[J]. Stud Plant Sci, 2019, 6:212-219. Yada H, Kimura T, Suzuki M, et al. New steroidal saponin from Hosta sieboldiana[J]. Biosci Biotechnol Biochem, 2010, 74(4):861-864. 吴晓, 刘银芳, 刘春宇. 沙苑子化学成分研究[J]. 安徽中医药大学学报, 2014, 33(3):91-94. Pistelli L, Noccioli C, Bertoli A, et al. Chemical composition and volatile constituents of Anthyllis barba-jovis[J]. Nat Prod Res, 2007, 21(5):418-425. 张援虎, 何丽, 关焕玉, 等. 追风伞中黄酮类成分的研究[J]. 中国中药杂志, 2010, 35(14):1824-1826. Su X C, Chen L, Aisa H A. Flavonoids and sterols from Alhagi sparsifolia[J]. Chem Nat Compd, 2008, 44(3):365. 张兴平, 周轶平, 缪晶茜, 等. 喙尾琵琶甲化学成分的研究[J]. 中草药, 2025, 56(4):1130-1137. 徐丹丹, 周洪波, 房志坚. 粗叶悬钩子的化学成分研究[J]. 广东药学院学报, 2012, 28(2):142-144. Zhong Y L, Zhang Y B, Luo D, et al. Two new compounds from Wedelia chinensis and their anti-inflammatory activities[J]. Chemistry Select, 2018, 3(12):3459-3462.)
Objective To investigate the chemical components in the Hosta plantaginea flower and evaluate their anti-inflammatory activities. Method The extraction was carried out using 95% and 70% ethanol aqueous solutions through percolation, followed by liquid-liquid extraction with petroleum ether and ethyl acetate. The chemical components were separated and purified by column chromatography methods such as D101 macroporous adsorption resin, silica gel, and ODS, as well as preparative liquid chromatography. Structural identification was conducted using high-resolution mass spectrometry, nuclear magnetic resonance spectroscopy, and circular dichroism spectrum (ECD). Moreover, the anti-inflammatory activities of all compounds were evaluated. Results Ten compounds were obtained from the aqueous layer of the H. plantaginea flower ethanol extract after extraction with ethyl acetate, including three steroids (1–3), four flavonoids (4–7), two alkaloids (8, 9), and one fatty acid (10). They were identified as (8S,9R,10S, 12S,13R,14R,16R,17S,20R,22S,25R,26R)-12,16-hydroxy-22,26-epoxy-26-methoxy-5α-cholest-4-en-3-one (or hostaspirone A, 1), (2α,3β,5α,25R)-2-hydroxyspirostan-3-yl O-β-D-glucopyranosyl-(1→2)-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (2), (25R)-3-(β-D-Glucopyranosyl-(1→2)-[β-D-xylopyranosyl-(1→3)]-β-D-glucopyranosyl-(1→4)-β-D-galactopyranosyl)-5-spirostan-2α-ol (3), rhamnocitrin-3-O-β-D-glucopyranoside (4), quercetin-3-O-β-glucopyranoside (5), isorhamnetin 3-O-glucoside (6), isorhamnetin-3-O-rutinoside (7), thymine (8), uracil (9), and myristic acid (10), respectively. Conclusion Compound 1 is the first steroid identified in this genus to exhibit an E-ring cleavage spirostan. Compounds 4, 6–8, and 10 were isolated for the first time from the family Asparagaceae, and compound 5 is reported here for the first time from the Hosta genus. In addition, compounds 1 and 4 have some anti-inflammatory effects. This study expands the chemical profile of H. plantaginea and provides a scientific foundation for its potential clinical applications.
YUAN Fang, XIA Bowei, YANG Li, LIU Kun, DENG Zitong, ZHANG Shouwen, HE Junwei.
A new E-ring cleavage spirostan isolated from Hosta plantaginea flower[J].
Chinese Traditional and Herbal Drugs,
2026
, 57
(8)
: 2981
-2988
.
DOI: 10.7501/j.issn.0253-2670.2026.08.011
基金
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中药资源可持续利用江西省重点实验室项目 (2024SSY07082)
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中国科学院中国植物志编辑委员会. 中国植物志 (第十四卷)[M]. 北京:科学出版社, 1980:49-50. Yang L, He J W. Traditional uses, phytochemistry, pharmacology and toxicological aspects of the genus Hosta (Liliaceae):A comprehensive review[J]. J Ethnopharmacol, 2021, 265:113323. He J W, Wang H L, Li X M, et al. Uncovering the benign prostatic hyperplasia protective mechanism of Hosta plantaginea flower fractions:AMPK/JAK pathways inhibition[J]. J Ethnopharmacol, 2025, 353(Pt B):120362. Li X M, Wang J S, Liang J, et al. Hosta plantaginea flower ameliorates chronic pharyngitis by suppressing inflammation via the JAK-STAT/PI3K/MAPK signaling axis in rats[J]. Chem Biodivers, 2025, 22(7):e202403254. Wang H L, Li X M, Xia B W, et al. Amelioration of chronic prostatitis by fractions of Mongolian medicine Hosta plantaginea flowers via inhibition of NF-κB, MAPKs, JAK-STAT, and PI3K-Akt signaling pathways in rats[J]. J Ethnopharmacol, 2023, 307:116245. Wang J S, Cao L, Wang H L, et al. Therapeutic effect of Hosta plantaginea (Lam.) Aschers flowers on acute pharyngitis through inhibition of multi-inflammatory pathways in rats[J]. J Ethnopharmacol, 2024, 318:116966. Wang H L, Mu Z Q, Liang J, et al. Hosta plantaginea (Lam.) Aschers flower modulates inflammation and amino acid metabolism by inhibiting NF-κB/MAPK/JAK-STAT/PI3K-Akt and AMPK pathways to alleviate benign prostatic hyperplasia in rats[J]. J Ethnopharmacol, 2025, 337:118970. Yang L, Zhang F X, He W W, et al. Extraction optimization and constituent analysis of total flavonoid from Hosta plantaginea (Lam.) Aschers flowers and its ameliorative effect on chronic prostatitis via inhibition of multiple inflammatory pathways in rats[J]. J Ethnopharmacol, 2024, 318:116922. Xia B W, Li X M, Zhang Q C, et al. Revealing the anti-inflammatory mechanism and effective constituents of Hosta plantaginea flowers by a strategy integrating network pharmacology, molecular docking, and experimental verification[J]. Eur J Integr Med, 2024, 71:102400. Yang L, He J W. Hosta plantaginea (Lam.) Aschers (Yuzan):An overview on its botany, traditional use, phytochemistry, quality control and pharmacology[J]. RSC Adv, 2019, 9(60):35050-35058. He J W, Yang L, Mu Z Q, et al. Anti-inflammatory and antioxidant activities of flavonoids from the flowers of Hosta plantaginea[J]. RSC Adv, 2018, 8(32):18175-18179. He J W, Huang X Y, Wang Y Q, et al. A new flavonol glycoside from the flowers of Hosta plantaginea with cyclooxygenases-1/2 inhibitory and antioxidant activities[J]. Nat Prod Res, 2019, 33(11):1599-1604. He J W, Guo P, Yang L, et al. Anti-inflammatory constituents isolated from the flowers of Hosta plantaginea via suppression of the NF-κB signaling pathway in LPS-stimulated RAW 264.7 macrophages[J]. RSC Adv, 2023, 13(11):7179-7184. Fang Y W, Yang L, He J W. Plantanone C attenuates LPS-stimulated inflammation by inhibiting NF-κB/iNOS/COX-2/MAPKs/Akt pathways in RAW 264.7 macrophages[J]. Biomed Pharmacother, 2021, 143:112104. Fang Y W, Wang H L, Xia X Y, et al. Kaempferol 3-O-(2G-glucosylrutinoside)-7-O-glucoside isolated from the flowers of Hosta plantaginea exerts anti-inflammatory activity via suppression of NF-κB, MAPKs and Akt pathways in RAW 264.7 cells[J]. Biomed Pharmacother, 2022, 153:113295. Yang L, Jiang S T, Zhou Q G, et al. Chemical constituents from the flower of Hosta plantaginea with cyclooxygenases inhibition and antioxidant activities and their chemotaxonomic significance[J]. Molecules, 2017, 22(11):1825. Yang L, Lin Y M, He Z W, et al. Hostaflavanol A, a new anti-inflammatory and antioxidant activities flavanol from the flowers of Hosta plantaginea[J]. Med Chem Res, 2020, 29(3):426-430. Yang L, Zhu Y Y, He Z W, et al. Plantanone D, a new rare methyl-flavonoid from the flowers of Hosta plantaginea with anti-inflammatory and antioxidant activities[J]. Nat Prod Res, 2021, 35(22):4331-4337. Yang Y T, Xia B W, Ouyang H, et al. Rapid two-step isolation of kaempferol from the Hosta plantaginea flower and its anti-inflammatory mechanism:Evidence from network pharmacology, molecular docking, molecular dynamics simulation, and experimental validation[J]. Separations, 2025, 12(6):138. Yang L, He J W. Anti-inflammatory effects of flavonoids and phenylethanoid glycosides from Hosta plantaginea flowers in LPS-stimulated RAW 264.7 macrophages through inhibition of the NF-κB signaling pathway[J]. BMC Complementary Med Ther, 2022, 22(1):55. Ksebati M B, Schmitz F J. Minabeolides:A group of withanolides from a soft coral, Minabea sp[J]. J Org Chem, 1988, 53(17):3926-3929. Li C S, Liu L X, Pan W T, et al. Potential chiral fluorescent molecular probes based on an α, β-unsaturated ketone for anion detection[J]. Sci Rep, 2019, 9(1):18838. Liu K Y, Yang J, Tang Y Y, et al. Bioassay-guided isolation of anti-leukemic steroids from Aglaia abbreviata by inducing apoptosis[J]. Bioorg Chem, 2024, 144:107147. Wang Y Q, Bao L, Yang X L, et al. Four new cuparene-type sesquiterpenes from Flammulina velutipes[J]. Helv Chim Acta, 2012, 95(2):261-267. Jiang Y, Wang N L, Yao X S, et al. Steroidal saponins from the bulbs of Allium chinense[J]. Stud Plant Sci, 2019, 6:212-219. Yada H, Kimura T, Suzuki M, et al. New steroidal saponin from Hosta sieboldiana[J]. Biosci Biotechnol Biochem, 2010, 74(4):861-864. 吴晓, 刘银芳, 刘春宇. 沙苑子化学成分研究[J]. 安徽中医药大学学报, 2014, 33(3):91-94. Pistelli L, Noccioli C, Bertoli A, et al. Chemical composition and volatile constituents of Anthyllis barba-jovis[J]. Nat Prod Res, 2007, 21(5):418-425. 张援虎, 何丽, 关焕玉, 等. 追风伞中黄酮类成分的研究[J]. 中国中药杂志, 2010, 35(14):1824-1826. Su X C, Chen L, Aisa H A. Flavonoids and sterols from Alhagi sparsifolia[J]. Chem Nat Compd, 2008, 44(3):365. 张兴平, 周轶平, 缪晶茜, 等. 喙尾琵琶甲化学成分的研究[J]. 中草药, 2025, 56(4):1130-1137. 徐丹丹, 周洪波, 房志坚. 粗叶悬钩子的化学成分研究[J]. 广东药学院学报, 2012, 28(2):142-144. Zhong Y L, Zhang Y B, Luo D, et al. Two new compounds from Wedelia chinensis and their anti-inflammatory activities[J]. Chemistry Select, 2018, 3(12):3459-3462.