Article(id=1304414863804092450, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414858296971266, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.06.003, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1766246400000, receivedDateStr=2025-12-21, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788926338386, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788926338386, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788926338386, creator=13701087609, updateTime=1788926338386, updator=13701087609, issue=Issue{id=1304414858296971266, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='6', pageStart='2009', pageEnd='2444', issueExtLink='null', onlineDate='null', pubDate='1774627200000', pubDateStr='2026-03-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788926337074, creator='13701087609', updateTime=1788926665348, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304416235240841997, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414858296971266, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304416235240841998, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414858296971266, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=2022, endPage=2028, ext={EN=ArticleExt(id=1304414865603448868, articleId=1304414863804092450, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=A new norsesquiterpenoid from Stemona tuberosa in Hainan, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical components and anti-inflammatory activities of the roots of Stemona tuberosa from Hainan province. Methods The chemical constituents of S. tuberosa were isolated and purified using chromatography techniques such as silica gel, gel column chromatography, and semi-preparative high-performance liquid chromatography (HPLC). Subsequently, the structures of the purified compounds were identified by modern spectroscopic methods such as nuclear magnetic resonance (NMR) and mass spectrometry (MS). Finally, the anti-inflammatory activities of the compounds were evaluated using the lipopolysaccharide (LPS)-induced murine monocyte-macrophage RAW264.7 cell model. Results A total of seven compounds were isolated from S. tuberosa, and identified as (4R)-3,5,5-trimethyl-4-(3-methylbut-2-enoyl)cyclohex-2-en-1-one (1 ), oxystemofoline (2 ), methyl 4-hydroxycinnamate (3 ), (-)-stemoamide (4 ), tuberostemospiroline (5 ), stemanthrene C (6 ), stilbostemin F (7 ). Compounds 2 and 3 exhibited inhibitory activity against NO production in LPS-induced RAW264.7 cells, with median inhibition concentration (IC50) values of (42.99 ± 4.96) and (70.22 ± 0.81) μmol/L, respectively. Conclusion Compound 1 was identified as a new compound, named tuberostemoterpenone. Compound 2 was isolated from S. tuberosa for the first time. Compounds 2 and 3 exhibited no significant cytotoxicity within the tested concentration range and demonstrated certain anti-inflammatory activity., authors=ZHU Xiongbo, XU Ruihua, WAN Bowen, WU Fei, WEI Yanmei, CAI Caihong, WANG Hao, DAI Haofu, MEI Wenli, HUANG Shengzhuo, WANG Ruozhong, authorsList=ZHU Xiongbo, XU Ruihua, WAN Bowen, WU Fei, WEI Yanmei, CAI Caihong, WANG Hao, DAI Haofu, MEI Wenli, HUANG Shengzhuo, WANG Ruozhong, 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=1304414865523757091, articleId=1304414863804092450, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=海南产对叶百部中1个新的降倍半萜, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究海南产对叶百部Stemona tuberosa根部的化学成分及其抗炎活性。方法 利用硅胶柱色谱、凝胶柱色谱、半制备高效液相色谱等色谱技术进行分离纯化,再通过核磁共振、质谱等现代波谱学方法进行鉴定,最后通过脂多糖诱导的小鼠单核巨噬细胞RAW264.7抗炎模型测试化合物的抗炎活性。结果 从海南产对叶百部根中分离鉴定得到7个化合物,分别为对叶百部萜酮(1)、羟基百部叶碱(2)、4-羟基肉桂酸甲酯(3)、(-)-百部酰胺(4)、(2S,4R,9'aS)-4-甲基八氢螺[氧杂环戊烷-2,9'-吡咯并[1,2-a]氮杂䓬]-3',5-二酮(5)、2,7-二羟基-4,8-二甲氧基-1,3-二甲基-9,10-二氢菲(6)、3-[2-(3-羟基-2-甲氧基苯基)乙基]-5-甲氧基-2-甲基苯酚(7)。化合物23具有抑制脂多糖诱导的RAW264.7细胞NO生成的活性,半数抑制浓度(median inhibition concentration,IC₅₀)值分别为(42.99±4.96)μmol/L和(70.22±0.81)μmol/L。结论 化合物1为新化合物,命名为对叶百部萜酮;化合物2为首次从海南产对叶百部中分离得到;化合物23在测试浓度范围内无明显细胞毒性且具有一定的抗炎活性。, authors=朱雄波1,2, 许瑞华2, 万博文2, 吴妃2, 魏艳梅2, 蔡彩虹2, 王昊2, 戴好富2,3, 梅文莉2,3, 黄圣卓2,3, 王若仲1, authorsList=朱雄波, 许瑞华, 万博文, 吴妃, 魏艳梅, 蔡彩虹, 王昊, 戴好富, 梅文莉, 黄圣卓, 王若仲, authorCompany=1 湖南农业大学生物科学技术学院 植物激素与生长发育湖南省重点实验室, 湖南 长沙 410128;
2 中国热带农业科学院热带生物技术研究所 海南省黎药资源天然产物研究与利用重点实验室, 海南 海口 571101;
3 中国热带农业科学院三亚研究院, 海南 三亚 572025, correspAuthors=null, authorNote=朱雄波: 朱雄波,男,硕士研究生,研究方向为天然产物化学。E-mail:zoobox@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=0MNQtxuhnG3JRO+N8QlIPw==, pdfFileSize=897455, 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=海南省重点研发项目 (ZDYF2024SHFZ063); 国家自然科学基金面上项目 (82373763); 国家热带农业科学中心科技创新团队 (CATASCXTD202521))}, authors=[Author(id=1307423890658054517, tenantId=1146029695717560320, journalId=null, articleId=1304414863804092450, orderNo=null, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=null, email=null, emailSecond=null, emailThird=null, correspondingAuthor=null, authorType=null, ext={}, 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中国药典[S]. 一部. 2025: 141-142.
Brem B, Seger C, Pacher T, et al. Feeding deterrence and contact toxicity of Stemona alkaloids-a source of potent natural insecticides[J]. J Agric Food Chem, 2002, 50(22): 6383-6388.
胡若瑛. 百部的植物来源及本草考证[J]. 四川中医, 1986, 4(12):33-34.
Nguyen-Thi C, Vo-Cong D, Giang L D, et al. Isolation and bioactivities of Stemona alkaloid: A review[J]. Nat Prod Commun, 2024, 19(5): 1934578X241255457.
Xu Y, Liang J M, Yan Y S, et al. The structure and bioactivities of Stemona alkaloids and alkaloids with[1, 2-α] azepine nucleus (2009-2021)[J]. Phytochem Rev, 2024, 23(3): 657-704.
Zhang N, Xu Y, Yue X Y, et al. Isolation, characterization and anti-inflammatory effect of alkaloids from the roots of Stemona tuberosa Lour[J]. Phytochemistry, 2024, 220: 114013.
Chen Y X, Peng X, Wang Z. Chemistry and biology of Stemona alkaloids[J]. Alkaloids Chem Biol, 2025, 94: 157-274.
Huang S Z, Kong F D, Chen G, et al. A phytochemical investigation of Stemona parviflora roots reveals several compounds with nematocidal activity[J]. Phytochemistry, 2019, 159: 208-215.
罗点. 对叶百部总生物碱HPLC-UPLC-MS指纹图谱建立及其与产地相关性的研究[D]. 南宁: 广西中医药大学, 2017.
罗点, 王晓彤, 吴思宇, 等. 全国不同产地对叶百部HPLC指纹图谱研究[J]. 广西中医药, 2017, 40(4): 72-77.
冯天龙, 黄灵芳, 许翔鸿, 等. 对叶百部药材中四种主要生物碱的分布规律[J]. 中国野生植物资源, 2018, 37(3): 42-47.
杨丹丹, 王晓彤, 吴思宇, 等. 对叶百部遗传多样性的AFLP分析[J]. 时珍国医国药, 2018, 29(10): 2519-2521.
王晓彤. 不同居群对叶百部遗传特征的比较与鉴别[D]. 南宁: 广西中医药大学, 2017.
Mi C N, Wang H, Chen H Q, et al. Polyacetylenes from the roots of Swietenia macrophylla King[J]. Molecules, 2019, 24(7): 1291.
Li M M, Su X Q, Sun J, et al. Anti-inflammatory ursane- and oleanane-type triterpenoids from Vitex negundo var. cannabifolia[J]. J Nat Prod, 2014, 77(10): 2248-2254.
Li Y L, Wang T, Wang H, et al. Nauclofficines A and B, two novel monoterpenoid indole alkaloids from the Li folk herb Nauclea officinalis with anti-allergic inflammatory effects on RBL-2H3 cells[J]. J Ethnopharmacol, 2025, 344: 119533.
Wang P, Chen X, Wang H, et al. Four new picrotoxane-type sesquiterpenes from Dendrobium nobile Lindl[J]. Front Chem, 2019, 7: 812.
Schoch E, Benda I, Schreier P. Bioconversion of alpha-damascone by Botrytis cinerea[J]. Appl Environ Microbiol, 1991, 57(1): 15-18.
林文翰, 徐任生, 钟琼芯. 百部生物碱的化学研究II.细花百部中微量生物碱的结构研究[J]. 化学学报, 1991, 49(10): 1034-1037.
Seifert K, Unger W. Insecticidal and fungicidal compounds from Isatis tinctoria[J]. Z Naturforsch C J Biosci, 1994, 49(1/2): 44-48.
Lin W H, Ye Y, Xu R S. Chemical studies on new Stemona alkaloids, IV. studies on new alkaloids from Stemona tuberosa[J]. J Nat Prod, 1992, 55(5): 571-576.
Jacobi P A, Lee K. Total syntheses of (±)- and (-)-stemoamide[J]. J Am Chem Soc, 2000, 122(18): 4295-4303.
Hu J P, Yang D H, Lin W H, et al. Alkaloids from the roots of Stemona tuberosa[J]. Helv Chim Acta, 2009, 92(10): 2125-2133.
Kostecki K, Engelmeier D, Pacher T, et al. Dihydrophenanthrenes and other antifungal stilbenoids from Stemona cf. pierrei [J]. Phytochemistry, 2004, 65(1): 99-106.
Pacher T, Seger C, Engelmeier D, et al. Antifungal stilbenoids from Stemona collinsae[J]. J Nat Prod, 2002, 65(6): 820-827.
Li H M, He T T, Zhang M, et al. Stilbenoids from the roots of Stemona tuberosa[J]. Nat Prod Res, 2022, 36(3): 695-700.
Qiu X, Geng Y, Cai X Y, et al. Anti-inflammatory activity and underlying mechanism against sepsis-induced acute lung injury of a low-molecular-weight polysaccharide from the root of Stemona tuberosa Lour[J]. Int J Biol Macromol, 2024, 282(Pt 1): 136617.)
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海南产对叶百部中1个新的降倍半萜
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中草药 | 化学成分 2026,57(6): 2022-2028
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中草药 |化学成分 2026 , 57 (6) : 2022 -2028
海南产对叶百部中1个新的降倍半萜
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作者简介:
朱雄波: 朱雄波,男,硕士研究生,研究方向为天然产物化学。E-mail:zoobox@qq.com
A new norsesquiterpenoid from Stemona tuberosa in Hainan
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doi: 10.7501/j.issn.0253-2670.2026.06.003
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目的 研究海南产对叶百部Stemona tuberosa根部的化学成分及其抗炎活性。方法 利用硅胶柱色谱、凝胶柱色谱、半制备高效液相色谱等色谱技术进行分离纯化,再通过核磁共振、质谱等现代波谱学方法进行鉴定,最后通过脂多糖诱导的小鼠单核巨噬细胞RAW264.7抗炎模型测试化合物的抗炎活性。结果 从海南产对叶百部根中分离鉴定得到7个化合物,分别为对叶百部萜酮(1)、羟基百部叶碱(2)、4-羟基肉桂酸甲酯(3)、(-)-百部酰胺(4)、(2S,4R,9'aS)-4-甲基八氢螺[氧杂环戊烷-2,9'-吡咯并[1,2-a]氮杂䓬]-3',5-二酮(5)、2,7-二羟基-4,8-二甲氧基-1,3-二甲基-9,10-二氢菲(6)、3-[2-(3-羟基-2-甲氧基苯基)乙基]-5-甲氧基-2-甲基苯酚(7)。化合物23具有抑制脂多糖诱导的RAW264.7细胞NO生成的活性,半数抑制浓度(median inhibition concentration,IC₅₀)值分别为(42.99±4.96)μmol/L和(70.22±0.81)μmol/L。结论 化合物1为新化合物,命名为对叶百部萜酮;化合物2为首次从海南产对叶百部中分离得到;化合物23在测试浓度范围内无明显细胞毒性且具有一定的抗炎活性。
对叶百部  /  生物碱  /  降倍半萜  /  抗炎活性  /  对叶百部萜酮  /  羟基百部叶碱  /  4-羟基肉桂酸甲酯
Objective To investigate the chemical components and anti-inflammatory activities of the roots of Stemona tuberosa from Hainan province. Methods The chemical constituents of S. tuberosa were isolated and purified using chromatography techniques such as silica gel, gel column chromatography, and semi-preparative high-performance liquid chromatography (HPLC). Subsequently, the structures of the purified compounds were identified by modern spectroscopic methods such as nuclear magnetic resonance (NMR) and mass spectrometry (MS). Finally, the anti-inflammatory activities of the compounds were evaluated using the lipopolysaccharide (LPS)-induced murine monocyte-macrophage RAW264.7 cell model. Results A total of seven compounds were isolated from S. tuberosa, and identified as (4R)-3,5,5-trimethyl-4-(3-methylbut-2-enoyl)cyclohex-2-en-1-one (1 ), oxystemofoline (2 ), methyl 4-hydroxycinnamate (3 ), (-)-stemoamide (4 ), tuberostemospiroline (5 ), stemanthrene C (6 ), stilbostemin F (7 ). Compounds 2 and 3 exhibited inhibitory activity against NO production in LPS-induced RAW264.7 cells, with median inhibition concentration (IC50) values of (42.99 ± 4.96) and (70.22 ± 0.81) μmol/L, respectively. Conclusion Compound 1 was identified as a new compound, named tuberostemoterpenone. Compound 2 was isolated from S. tuberosa for the first time. Compounds 2 and 3 exhibited no significant cytotoxicity within the tested concentration range and demonstrated certain anti-inflammatory activity.
Stemona tuberosa Lour.  /  alkaloids  /  norsesquiterpenoids  /  anti-inflammatory activity  /  tuberostemoterpenone  /  oxystemofoline  /  methyl 4-hydroxycinnamate
朱雄波, 许瑞华, 万博文, 吴妃, 魏艳梅, 蔡彩虹, 王昊, 戴好富, 梅文莉, 黄圣卓, 王若仲. 海南产对叶百部中1个新的降倍半萜. 中草药, 2026 , 57 (6) : 2022 -2028 . DOI: 10.7501/j.issn.0253-2670.2026.06.003
ZHU Xiongbo, XU Ruihua, WAN Bowen, WU Fei, WEI Yanmei, CAI Caihong, WANG Hao, DAI Haofu, MEI Wenli, HUANG Shengzhuo, WANG Ruozhong. A new norsesquiterpenoid from Stemona tuberosa in Hainan[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (6) : 2022 -2028 . DOI: 10.7501/j.issn.0253-2670.2026.06.003

    海南省重点研发项目 (ZDYF2024SHFZ063); 国家自然科学基金面上项目 (82373763); 国家热带农业科学中心科技创新团队 (CATASCXTD202521)

参考文献 引证文献
排序方式:
Kaltenegger E, Brem B, Mereiter K, et al. Insecticidal pyrido[1, 2-a] azepine alkaloids and related derivatives from Stemona species[J]. Phytochemistry, 2003, 63(7): 803-816.
秦燕, 王跃华, 孙卫邦, 等. 百部科植物叶表皮特征及其分类学意义[J]. 植物科学学报, 2018, 36(4): 487-500.
中国药典[S]. 一部. 2025: 141-142.
Brem B, Seger C, Pacher T, et al. Feeding deterrence and contact toxicity of Stemona alkaloids-a source of potent natural insecticides[J]. J Agric Food Chem, 2002, 50(22): 6383-6388.
胡若瑛. 百部的植物来源及本草考证[J]. 四川中医, 1986, 4(12):33-34.
Nguyen-Thi C, Vo-Cong D, Giang L D, et al. Isolation and bioactivities of Stemona alkaloid: A review[J]. Nat Prod Commun, 2024, 19(5): 1934578X241255457.
Xu Y, Liang J M, Yan Y S, et al. The structure and bioactivities of Stemona alkaloids and alkaloids with[1, 2-α] azepine nucleus (2009-2021)[J]. Phytochem Rev, 2024, 23(3): 657-704.
Zhang N, Xu Y, Yue X Y, et al. Isolation, characterization and anti-inflammatory effect of alkaloids from the roots of Stemona tuberosa Lour[J]. Phytochemistry, 2024, 220: 114013.
Chen Y X, Peng X, Wang Z. Chemistry and biology of Stemona alkaloids[J]. Alkaloids Chem Biol, 2025, 94: 157-274.
Huang S Z, Kong F D, Chen G, et al. A phytochemical investigation of Stemona parviflora roots reveals several compounds with nematocidal activity[J]. Phytochemistry, 2019, 159: 208-215.
罗点. 对叶百部总生物碱HPLC-UPLC-MS指纹图谱建立及其与产地相关性的研究[D]. 南宁: 广西中医药大学, 2017.
罗点, 王晓彤, 吴思宇, 等. 全国不同产地对叶百部HPLC指纹图谱研究[J]. 广西中医药, 2017, 40(4): 72-77.
冯天龙, 黄灵芳, 许翔鸿, 等. 对叶百部药材中四种主要生物碱的分布规律[J]. 中国野生植物资源, 2018, 37(3): 42-47.
杨丹丹, 王晓彤, 吴思宇, 等. 对叶百部遗传多样性的AFLP分析[J]. 时珍国医国药, 2018, 29(10): 2519-2521.
王晓彤. 不同居群对叶百部遗传特征的比较与鉴别[D]. 南宁: 广西中医药大学, 2017.
Mi C N, Wang H, Chen H Q, et al. Polyacetylenes from the roots of Swietenia macrophylla King[J]. Molecules, 2019, 24(7): 1291.
Li M M, Su X Q, Sun J, et al. Anti-inflammatory ursane- and oleanane-type triterpenoids from Vitex negundo var. cannabifolia[J]. J Nat Prod, 2014, 77(10): 2248-2254.
Li Y L, Wang T, Wang H, et al. Nauclofficines A and B, two novel monoterpenoid indole alkaloids from the Li folk herb Nauclea officinalis with anti-allergic inflammatory effects on RBL-2H3 cells[J]. J Ethnopharmacol, 2025, 344: 119533.
Wang P, Chen X, Wang H, et al. Four new picrotoxane-type sesquiterpenes from Dendrobium nobile Lindl[J]. Front Chem, 2019, 7: 812.
Schoch E, Benda I, Schreier P. Bioconversion of alpha-damascone by Botrytis cinerea[J]. Appl Environ Microbiol, 1991, 57(1): 15-18.
林文翰, 徐任生, 钟琼芯. 百部生物碱的化学研究II.细花百部中微量生物碱的结构研究[J]. 化学学报, 1991, 49(10): 1034-1037.
Seifert K, Unger W. Insecticidal and fungicidal compounds from Isatis tinctoria[J]. Z Naturforsch C J Biosci, 1994, 49(1/2): 44-48.
Lin W H, Ye Y, Xu R S. Chemical studies on new Stemona alkaloids, IV. studies on new alkaloids from Stemona tuberosa[J]. J Nat Prod, 1992, 55(5): 571-576.
Jacobi P A, Lee K. Total syntheses of (±)- and (-)-stemoamide[J]. J Am Chem Soc, 2000, 122(18): 4295-4303.
Hu J P, Yang D H, Lin W H, et al. Alkaloids from the roots of Stemona tuberosa[J]. Helv Chim Acta, 2009, 92(10): 2125-2133.
Kostecki K, Engelmeier D, Pacher T, et al. Dihydrophenanthrenes and other antifungal stilbenoids from Stemona cf. pierrei [J]. Phytochemistry, 2004, 65(1): 99-106.
Pacher T, Seger C, Engelmeier D, et al. Antifungal stilbenoids from Stemona collinsae[J]. J Nat Prod, 2002, 65(6): 820-827.
Li H M, He T T, Zhang M, et al. Stilbenoids from the roots of Stemona tuberosa[J]. Nat Prod Res, 2022, 36(3): 695-700.
Qiu X, Geng Y, Cai X Y, et al. Anti-inflammatory activity and underlying mechanism against sepsis-induced acute lung injury of a low-molecular-weight polysaccharide from the root of Stemona tuberosa Lour[J]. Int J Biol Macromol, 2024, 282(Pt 1): 136617.
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doi: 10.7501/j.issn.0253-2670.2026.06.003
  • 接收时间:2025-12-21
  • 首发时间:2026-09-09
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2种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

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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