Article(id=1322631248560902461, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631228000424183, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.18.012, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1783440000000, receivedDateStr=2026-07-08, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793269462956, onlineDateStr=2026-10-29, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793269462956, onlineIssueDateStr=2026-10-29, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793269462956, creator=13701087609, updateTime=1793269462956, updator=13701087609, issue=Issue{id=1322631228000424183, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='18', pageStart='7073', pageEnd='7500', issueExtLink='null', onlineDate='null', pubDate='1790524800000', pubDateStr='2026-09-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1793269458054, creator='13701087609', updateTime=1793269548245, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322631606339228314, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631228000424183, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322631606339228315, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1322631228000424183, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=7226, endPage=7232, ext={EN=ArticleExt(id=1322631249852748097, articleId=1322631248560902461, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=A new steroid from Physalis angulata and its anti-inflammatory activity, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical constituents from the whole plant of Physalis angulata and their anti-inflammatory activities. Methods Various chromatographic techniques were employed for the isolation and purification of compounds, and their structures were elucidated by spectroscopic methods including NMR, MS, and UV. The cytotoxicity against mouse macrophage RAW264.7 cells was evaluated using the SRB assay, while the in vitro anti-inflammatory activity was determined via the Griess assay. Results Five compounds were isolated from the methanol extract of the whole plant of P. angulata and identified as 6- 5β,6β:14α,17:14β,26-triepoxy-13α,15β-dihydroxy-1-keto-11,15-cyclo-13,14-secoergostan-2-en-18,26-olide (1), physalin B (2), physalin F (3), physalin XI (4), and aspergillus triazolate A (5). Compounds 2—5 exhibited inhibitory effects on NO production in RAW264.7 cells, with IC50 values ranging from (1.97 ± 0.12) to (6.73 ± 0.71) μmol/L. Conclusion Compound 1 is a new compound, named 5,6-epoxyphysalin IX. Compounds 4 and 5 showed significant anti-inflammatory activities., authors=HE Yue1, HUANG Jielin1, SHEN Huiling1, XU Lili1, YIN Junlin1, authorsList=HE Yue, HUANG Jielin, SHEN Huiling, XU Lili, YIN Junlin, authorCompany=1 Yunnan Key Laboratory of Chiral Functional Substance Research and Application, Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, School of Chemistry and Environment/School of Ethnic Medicine, Yunnan Minzu University, Kunming 650500, 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=1322631249588506944, articleId=1322631248560902461, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=苦蘵中1个新的甾体类化合物及其抗炎活性, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究苦蘵Physalis angulata全株的化学成分及其抗炎活性。方法 综合运用多种色谱技术进行化合物的分离纯化,结合核磁共振、质谱及紫外光谱等波谱学方法鉴定其结构;采用SRB法评价化合物对小鼠巨噬细胞RAW264.7的细胞毒性,同时通过Griess法测定其体外抗炎活性。结果 从苦蘵全株的甲醇提取物中分离得到5个化合物,分别鉴定为6-5β,6β:14α,17:14β,26-三环氧-13α,15β-二羟基-1-酮-11,15-环-13,14-开环麦角甾烷-2-烯-18,26-内酯(1)、酸浆苦素B(2)、酸浆苦素F(3)、酸浆苦素XI(4)、烟曲霉三唑酯A(5)。化合物2~5具有抑制RAW264.7细胞NO生成的活性,半数抑制浓度(median inhibition concentration,IC₅₀)值为(1.97±0.12)~(6.73±0.71)mmol/L。结论 化合物1为新化合物,命名为5,6-环氧酸浆苦素IX;化合物4、5具有显著的抗炎活性。, authors=何月1, 黄杰林1, 沈惠玲1, 徐丽丽1, 尹俊林1, authorsList=何月, 黄杰林, 沈惠玲, 徐丽丽, 尹俊林, authorCompany=1 云南民族大学 化学与环境学院/民族医药学院 民族药资源化学国家民委-教育部重点实验室 云南省手性功能物质研究与应用重点实验室, 云南 昆明 650500, correspAuthors=徐丽丽, authorNote=何月: 何月,女,硕士研究生,主要从事天然药物化学及其生物活性研究。E-mail:1679224399@qq.com, 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钱亚芳,杨波,冯迪,等.“靶点+活性”快速发现苦蘵中靶向Hsp90抗胰腺癌有效成分的研究[J]. 药学学报, 2019, 54(3):475-481.
Sun L J, Zhou L, Chen M C, et al. Amelioration of systemic lupus erythematosus by withangulatin A in MRL/lpr mice[J]. J Cell Biochem, 2011, 112(9):2376-2382.
Meira C S, Guimarães E T, Bastos T M, et al. Physalins B and F, seco-steroids isolated from Physalis angulate L.,strongly inhibit proliferation, ultrastructure and infectivity of Trypanosoma cruzi[J]. Parasitology, 2013, 140(14):1811-1821.
赵国平.中药大辞典[M]. 2版.上海:上海科学技术出版社, 2006:836.
Yu T J, Cheng Y B, Lin L C, et al. Physalis peruvianaderived physapruin a(PHA)inhibits breast cancer cell proliferation and induces oxidative-stress-mediated apoptosis and DNA damage[J]. Antioxidants, 2021, 10(3):393.
Vieceli P S, Juiz P J L, Lauria P S S, et al. Physalis angulata reduces the progression of chronic experimental periodontitis by immunomodulatory mechanisms[J]. J Ethnopharmacol, 2021, 273:113986.
Bauer J A, Sysel A M, Heston A J, et al. Standardized sulforhodamine b colorimetric cell proliferation assay for anticancer activity screening in educational and research laboratories[J]. MethodsX, 2025, 15:103469.
邓茂鑫,张洪川,马开悦,等.双参的化学成分及抗炎活性研究[J]. 中草药, 2026, 57(8):2989-2999.
Sun C P, Qiu C Y, Zhao F, et al. Physalins V-IX, 16, 24-cyclo-13, 14-seco withanolides from Physalis angulata and their antiproliferative and anti-inflammatory activities[J]. Sci Rep, 2017, 7:4057.
许枬,王冰,周翎,等.酸浆化学成分的研究[J]. 中草药, 2009, 40(2):175-178.
Fang L Q, Chai H B, Castillo J J, et al. Cytotoxic constituents of Brachistus stramoniifolius[J]. Phytother Res, 2003, 17(5):520-523.
Boonsombat J, Chawengrum P, Mahidol C, et al. A new22, 26-seco physalin steroid from Physalis angulata[J]. Nat Prod Res, 2020, 34(8):1097-1104.
陈彦君,祝丽君,于红梅,等.霸王鞭内生真菌烟曲霉中1个新的生物碱类化合物[J]. 中草药, 2019, 50(22):5400-5403.)
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苦蘵中1个新的甾体类化合物及其抗炎活性
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中草药 | 化学成分 2026,57(18): 7226-7232
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中草药 |化学成分 2026 , 57 (18) : 7226 -7232
苦蘵中1个新的甾体类化合物及其抗炎活性
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何月1, 黄杰林1, 沈惠玲1, 徐丽丽1, 尹俊林1
作者信息
    1 云南民族大学 化学与环境学院/民族医药学院 民族药资源化学国家民委-教育部重点实验室 云南省手性功能物质研究与应用重点实验室, 云南 昆明 650500
通讯作者:
徐丽丽
作者简介:
何月: 何月,女,硕士研究生,主要从事天然药物化学及其生物活性研究。E-mail:1679224399@qq.com
A new steroid from Physalis angulata and its anti-inflammatory activity
  • HE Yue1, HUANG Jielin1, SHEN Huiling1, XU Lili1, YIN Junlin1
  • Affiliations
      1 Yunnan Key Laboratory of Chiral Functional Substance Research and Application, Key Laboratory of Chemistry in Ethnic Medicinal Resources, State Ethnic Affairs Commission & Ministry of Education, School of Chemistry and Environment/School of Ethnic Medicine, Yunnan Minzu University, Kunming 650500, China
    doi: 10.7501/j.issn.0253-2670.2026.18.012
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    目的 研究苦蘵Physalis angulata全株的化学成分及其抗炎活性。方法 综合运用多种色谱技术进行化合物的分离纯化,结合核磁共振、质谱及紫外光谱等波谱学方法鉴定其结构;采用SRB法评价化合物对小鼠巨噬细胞RAW264.7的细胞毒性,同时通过Griess法测定其体外抗炎活性。结果 从苦蘵全株的甲醇提取物中分离得到5个化合物,分别鉴定为6-5β,6β:14α,17:14β,26-三环氧-13α,15β-二羟基-1-酮-11,15-环-13,14-开环麦角甾烷-2-烯-18,26-内酯(1)、酸浆苦素B(2)、酸浆苦素F(3)、酸浆苦素XI(4)、烟曲霉三唑酯A(5)。化合物2~5具有抑制RAW264.7细胞NO生成的活性,半数抑制浓度(median inhibition concentration,IC₅₀)值为(1.97±0.12)~(6.73±0.71)mmol/L。结论 化合物1为新化合物,命名为5,6-环氧酸浆苦素IX;化合物4、5具有显著的抗炎活性。
    酸浆属  /  苦蘵  /  甾体  /  5,6-环氧酸浆苦素IX  /  酸浆苦素B  /  酸浆苦素XI  /  烟曲霉三唑酯A  /  抗炎活性
    Objective To investigate the chemical constituents from the whole plant of Physalis angulata and their anti-inflammatory activities. Methods Various chromatographic techniques were employed for the isolation and purification of compounds, and their structures were elucidated by spectroscopic methods including NMR, MS, and UV. The cytotoxicity against mouse macrophage RAW264.7 cells was evaluated using the SRB assay, while the in vitro anti-inflammatory activity was determined via the Griess assay. Results Five compounds were isolated from the methanol extract of the whole plant of P. angulata and identified as 6- 5β,6β:14α,17:14β,26-triepoxy-13α,15β-dihydroxy-1-keto-11,15-cyclo-13,14-secoergostan-2-en-18,26-olide (1), physalin B (2), physalin F (3), physalin XI (4), and aspergillus triazolate A (5). Compounds 2—5 exhibited inhibitory effects on NO production in RAW264.7 cells, with IC50 values ranging from (1.97 ± 0.12) to (6.73 ± 0.71) μmol/L. Conclusion Compound 1 is a new compound, named 5,6-epoxyphysalin IX. Compounds 4 and 5 showed significant anti-inflammatory activities.
    Physalis L.  /  Physalis angulate L.  /  steroids  /  5,6-epoxyphysalin IX  /  physalin B  /  physalin XI  /  aspergillus triazolate A  /  anti-inflammatory activity
    何月, 黄杰林, 沈惠玲, 徐丽丽, 尹俊林. 苦蘵中1个新的甾体类化合物及其抗炎活性. 中草药, 2026 , 57 (18) : 7226 -7232 . DOI: 10.7501/j.issn.0253-2670.2026.18.012
    HE Yue, HUANG Jielin, SHEN Huiling, XU Lili, YIN Junlin. A new steroid from Physalis angulata and its anti-inflammatory activity[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (18) : 7226 -7232 . DOI: 10.7501/j.issn.0253-2670.2026.18.012

      国家自然科学基金项目 (21768005); 国家自然科学基金项目 (82660967)

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    Zhang J H, Xu X, Zhao Y, et al. Target separation and potential anticancer activity of withanolide-based glucose transporter protein 1 inhibitors from Physalis angulata var.villosa[J]. J Nat Prod, 2024, 87(1):2-13.
    钱亚芳,杨波,冯迪,等.“靶点+活性”快速发现苦蘵中靶向Hsp90抗胰腺癌有效成分的研究[J]. 药学学报, 2019, 54(3):475-481.
    Sun L J, Zhou L, Chen M C, et al. Amelioration of systemic lupus erythematosus by withangulatin A in MRL/lpr mice[J]. J Cell Biochem, 2011, 112(9):2376-2382.
    Meira C S, Guimarães E T, Bastos T M, et al. Physalins B and F, seco-steroids isolated from Physalis angulate L.,strongly inhibit proliferation, ultrastructure and infectivity of Trypanosoma cruzi[J]. Parasitology, 2013, 140(14):1811-1821.
    赵国平.中药大辞典[M]. 2版.上海:上海科学技术出版社, 2006:836.
    Yu T J, Cheng Y B, Lin L C, et al. Physalis peruvianaderived physapruin a(PHA)inhibits breast cancer cell proliferation and induces oxidative-stress-mediated apoptosis and DNA damage[J]. Antioxidants, 2021, 10(3):393.
    Vieceli P S, Juiz P J L, Lauria P S S, et al. Physalis angulata reduces the progression of chronic experimental periodontitis by immunomodulatory mechanisms[J]. J Ethnopharmacol, 2021, 273:113986.
    Bauer J A, Sysel A M, Heston A J, et al. Standardized sulforhodamine b colorimetric cell proliferation assay for anticancer activity screening in educational and research laboratories[J]. MethodsX, 2025, 15:103469.
    邓茂鑫,张洪川,马开悦,等.双参的化学成分及抗炎活性研究[J]. 中草药, 2026, 57(8):2989-2999.
    Sun C P, Qiu C Y, Zhao F, et al. Physalins V-IX, 16, 24-cyclo-13, 14-seco withanolides from Physalis angulata and their antiproliferative and anti-inflammatory activities[J]. Sci Rep, 2017, 7:4057.
    许枬,王冰,周翎,等.酸浆化学成分的研究[J]. 中草药, 2009, 40(2):175-178.
    Fang L Q, Chai H B, Castillo J J, et al. Cytotoxic constituents of Brachistus stramoniifolius[J]. Phytother Res, 2003, 17(5):520-523.
    Boonsombat J, Chawengrum P, Mahidol C, et al. A new22, 26-seco physalin steroid from Physalis angulata[J]. Nat Prod Res, 2020, 34(8):1097-1104.
    陈彦君,祝丽君,于红梅,等.霸王鞭内生真菌烟曲霉中1个新的生物碱类化合物[J]. 中草药, 2019, 50(22):5400-5403.
    2026年第57卷第18期
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    doi: 10.7501/j.issn.0253-2670.2026.18.012
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    2种不同金属材料的力学参数
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    属数
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    genus
    种数
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    species
    占总种数比例
    Percentage of
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    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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