Article(id=1304414867159535668, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414858296971266, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.06.002, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1768060800000, receivedDateStr=2026-01-11, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788926339187, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788926339187, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788926339187, creator=13701087609, updateTime=1788926339187, 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=2016, endPage=2021, ext={EN=ArticleExt(id=1304414867469914166, articleId=1304414867159535668, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Biphenyl compounds isolated from Garcinia yunnanensis , columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the biphenyl compounds in the ethyl acetate-soluble fraction of the twigs of Garcinia yunnanensis . Methods Based on the UV spectral characteristics absorption of biphenyl derivatives, targeted separation and purification were performed using various chromatography techniques, including silica gel column chromatography, Sephadex LH-20 gel column and semi-preparative HPLC. The structures of the isolated compounds were elucidated by means of physicochemical properties and spectral data of the monomer compounds, in combination with relevant literature. The anti-inflammatory activity of the new compound was evaluated by measuring its inhibition effect of nitric oxide (NO) production. Results Eight bipheny derivatives were obtained from the ethyl acetate fraction of G. yunnanensis , elucidated as (R )-5-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-2,3-dihydrobenzofuran-7-ol (1 ), garcibiphenyl C (2 ), cylindrobiphenyl B (3 ), multibiphenyl C (4 ), doitungbiphenyls B (5 ), multiflorabiphenyl B (6 ), honokiol (7 ), and magnolol (8 ). Conclusion Compound 1 is a new compound named yunnabiphenyl A, while compounds 2 —8 were reported from this plant for the first time. Compound 1 showed moderate anti-inflammatory activity, with a median inhibition concentration (IC50 ) value of 21.5 μmol/L., authors=YU Yue, CHEN Yu, PENG Caiying, LIANG Yonghong, LIU Jianqun, SHU Jicheng, authorsList=YU Yue, CHEN Yu, PENG Caiying, LIANG Yonghong, LIU Jianqun, SHU Jicheng, 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=1304414867386028085, articleId=1304414867159535668, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=云南藤黄中联苯类成分研究, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究云南藤黄Garcinia yunnanensis 枝叶醋酸乙酯部位中联苯类化学成分。方法 基于联苯衍生物的紫外光谱特征吸收,综合采用正相硅胶柱、Sephadex LH-20 凝胶柱和半制备HPLC等方法进行目标分离纯化。依据单体化合物的理化性质与波谱数据,并结合相关文献进行结构鉴定。通过抑制一氧化氮生成实验,评价新化合物的抗炎活性。结果 从云南藤黄醋酸乙酯部位中分离得到8个联苯类成分,分别鉴定为 (R )-5-(4-羟基苯基)-2-(2-羟基丙基)-2,3-二氢苯并呋喃-7-醇(1 )、garcibiphenyl C(2 )、cylindrobiphenyl B(3 )、multibiphenyl C(4 )、doitungbiphenyls B(5 )、multiflorabiphenyl B(6 )、和厚朴酚(7 )和厚朴酚(8 )。结论 化合物1 为新化合物,命名为藤黄联苯A(yunnabiphenyl A);化合物2 ~8 均为首次从该植物中分离得到。化合物1 显示一定的抗炎活性,其半数抑制浓度(median inhibition concentration,IC₅₀)为21.5μmol/L。, authors=余越1 , 陈煜2 , 彭财英1 , 梁永红1 , 刘建群1 , 舒积成1 , authorsList=余越, 陈煜, 彭财英, 梁永红, 刘建群, 舒积成, authorCompany=1 江西中医药大学, 现代中药制剂教育部重点实验室, 江西 南昌 330004; 2 中国医学科学院北京协和医学院医药生物技术研究所, 国家新药微生物筛选实验室, 北京 100050, correspAuthors=null, authorNote=余越: 余越(2001-),男,硕士研究生,从事中药药效物质基础研究。E-mail:741563518@qq.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=6dvExOPsVEtKfB5rSu6+1w==, pdfFileSize=979496, 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=国家自然科学基金资助项目 (82160660); 江西省自然科学基金资助项目 (20212ACB206006); 江西中医药大学“1050”工程人才项目 (5142001004))}, authors=null, keywords=[Keyword(id=1304414867595743287, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304414867159535668, language=CN, orderNo=1, keyword=云南藤黄), Keyword(id=1304414867671240760, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304414867159535668, language=CN, orderNo=2, keyword=联苯), Keyword(id=1304414867729961017, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304414867159535668, language=CN, orderNo=3, keyword=抗炎), Keyword(id=1304414867797069882, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304414867159535668, language=CN, orderNo=4, keyword=藤黄联苯A), Keyword(id=1304414867889344571, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304414867159535668, language=CN, orderNo=5, keyword=和厚朴酚), Keyword(id=1304414867969036348, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304414867159535668, language=CN, orderNo=6, keyword=厚朴酚), Keyword(id=1304414868048728125, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304414867159535668, language=CN, orderNo=7, keyword=garcibiphenyl C), Keyword(id=1304414868145197118, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304414867159535668, language=EN, orderNo=1, keyword=Garcinia yunnanensis H. 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Boonyong C, Pattamadilok C, Suttisri R, et al . Benzophenones and xanthone derivatives from Garcinia schomburgkiana -induced P-glycoprotein overexpression in human colorectal Caco-2 cells via oxidative stress-mediated mechanisms[J]. Phytomedicine , 2017, 27: 8-14. Shahid M, Law D, Azfaralariff A, et al . Phytochemicals and biological activities of Garcinia atroviridis : A critical review[J]. Toxics , 2022, 10(11): 656. Rizaldy D, Hartati R, Nadhifa TFI. Chemical compounds and pharmacological activities of Mangosteen (Garcinia mangostana L.)-updated review[J]. Biointerface Res App , 2022, 12(2): 2503-2516. Fu Y G, Huang Y Q, Xu Z H, et al . Polyprenylated acylphloroglucinols from Garcinia species and structural revision of seven analogues[J]. Nat Prod Bioprospect , 2025, 15(1): 34. Lim S H, Lee H S, Lee C H, et al . Pharmacological activity of Garcinia indica (kokum): An updated review[J]. Pharmaceuticals , 2021, 14(12): 1338. Hu X Y, Luo H J, Wei X, et al . Anti-inflammatory bicyclic polyprenylated acylphloroglucinols with diverse architectures including an unprecedented 6/6/6 tricyclic core from Garcinia yunnanensis [J]. Bioorg Chem , 2024, 153: 107864. Nan M M, Yang Y Y, Ying P, et al . Garciyunnanones A-R: Caged polycyclic polyprenylated acylphloroglucinols decorated with a lavandulyl substituent from Garcinia yunnanensis [J]. Phytochemistry , 2024, 224: 114167. Wang S, Liu S Y, Wang S, et al . Garciyndiphenyls a and B, two biphenyl dimers with a caged skeleton from Garcinia yunnanensis [J]. Org Lett , 2025, 27(14): 3800-3805. Chen J J, Peng C F, Huang H Y, et al . Benzopyrans, biphenyls and xanthones from the root of Garcinia linii and their activity against Mycobacterium tuberculosis[J]. Planta Med , 2006, 72(5): 473-477. Mungmee C, Sitthigool S, Buakeaw A, et al . A new biphenyl and other constituents from the wood of Garcinia schomburgkiana [J]. Nat Prod Res , 2013, 27(21): 1949-1955. Li Y K, Wang Z Y, Wu X X, et al . Biphenyl derivatives from the twigs of Garcinia bracteata and their biological activities[J]. Phytochem Lett , 2015, 11: 24-27. Kim C S, Subedi L, Kwon O K, et al . Isolation of bioactive biphenyl compounds from the twigs of Chaenomeles sinensis [J]. Bioorg Med Chem Lett , 2016, 26(2): 351-354. Zheng D, Zhang H, Jiang J M, et al . Prenylated xanthones and biphenyls from Garcinia esculenta with antistaphylococcal activity[J]. Nat Prod Res , 2021, 35(13): 2137-2144. Gao X M, Cui D, Wang S S, et al . New biphenyls from Garcinia lancilimba [J]. Phytochem Lett , 2018, 27: 219-222. Pailee P, Kuhakarn C, Sangsuwan C, et al . Anti-HIV and cytotoxic biphenyls, benzophenones and xanthones from stems, leaves and twigs of Garcinia speciosa [J]. Phytochemistry , 2018, 147: 68-79. Tian D S, Gu W, Wang L P, et al . Cytotoxic and anti-oxidant biphenyl derivatives from the leaves and twigs of Garcinia multiflora [J]. Phytochem Lett , 2017, 19: 132-135. Auranwiwat C, Limtharakul T, Pyne S G, et al . A new xanthone and a biphenyl from the flower and twig extracts of Garcinia mckeaniana [J]. Nat Prod Res , 2021, 35(20): 3404-3409. Chaturonrutsamee S, Kuhakarn C, Surawatanawong P, et al . Polycyclic polyprenylated acylphloroglucinols and biphenyl derivatives from the roots of Garcinia nuntasaenii Ngerns. & Suddee[J]. Phytochemistry , 2018, 146: 63-74. 李圆圆, 卢炜仁, 黄慧莲, 等. 欧洲蕨中8-2' 连接的木脂素类成分研究[J]. 中草药, 2025, 56(21): 7675-7679. Asai T, Luo D, Obara Y, et al . Dihydrobenzofurans as cannabinoid receptor ligands from Cordyceps annullata , an entomopathogenic fungus cultivated in the presence of an HDAC inhibitor[J]. Tetrahedron Lett , 2012, 53(17): 2239-2243. Antus S, Kurtán T, Juhász L, et al . Chiroptical properties of 2, 3-dihydrobenzo[b] furan and chromane chromophores in naturally occurring O -heterocycles[J]. Chirality , 2001, 13(8): 493-506. Chen J J, Peng C F, Huang H Y, et al . Benzopyrans, biphenyls and xanthones from the root of Garcinia linii and their activity against Mycobacterium tuberculosis [J]. Planta Med , 2006, 72(5): 473-477. Sukandar E R, Kaennakam S, Rassamee K, et al . Xanthones and biphenyls from the stems of Garcinia cylindrocarpa and their cytotoxicity[J]. Fitoterapia , 2018, 130: 112-117. Gao X M, Ji B K, Li Y K, et al . New biphenyls from Garcinia multiflora [J]. J Braz Chem Soc , 2015: 27(1): 10-14. Siridechakorn I, Maneerat W, Sripisut T, et al . Biphenyl and xanthone derivatives from the twigs of a Garcinia sp. (Clusiaceae)[J]. Phytochem Lett , 2014, 8: 77-80. Fu W W, Wu M, Zhu L L, et al . Prenylated benzoylphloroglucinols and biphenyl derivatives from the leaves of Garcinia multiflora Champ[J]. RSC Adv , 2015, 5(95): 78259-78267. 邓世明, 程永现, 周俊, 等. 长缘厚朴中的新苯醌及新木脂素类化合物[J]. 云南植物研究, 2001, 23(1): 121-125. Suh W S, Park K J, Kim D H, et al . A biphenyl derivative from the twigs of Chaenomeles speciosa [J]. Bioorg Chem , 2017, 72: 156-160. Phukhatmuen P, Raksat A, Laphookhieo S, et al . Bioassay-guided isolation and identification of antidiabetic compounds from Garcinia cowa leaf extract[J]. Heliyon , 2020, 6(4): e03625. Takaoka S, Nakade K, Fukuyama Y. The first total synthesis and neurotrophic activity of clusiparalicoline A, a prenylated and geranylated biaryl from Clusia paralicola [J]. Tetrahedron Lett , 2002, 43(39): 6919-6923. Zhang X C, Gao R R, Liu Y, et al . Anti-virulence activities of biflavonoids from Mesua ferrea L. flower[J]. Drug Discov Ther , 2019, 13(4): 222-227.)
中草药
|化学成分
2026
, 57
(6) :
2016
-2021
云南藤黄中联苯类成分研究
全屏
余越1 , 陈煜2 , 彭财英1 , 梁永红1 , 刘建群1 , 舒积成1
作者信息
1 江西中医药大学, 现代中药制剂教育部重点实验室, 江西 南昌 330004; 2 中国医学科学院北京协和医学院医药生物技术研究所, 国家新药微生物筛选实验室, 北京 100050
作者简介:
余越: 余越(2001-),男,硕士研究生,从事中药药效物质基础研究。E-mail:741563518@qq.com
Biphenyl compounds isolated from Garcinia yunnanensis
YU Yue, CHEN Yu, PENG Caiying, LIANG Yonghong, LIU Jianqun, SHU Jicheng
Affiliations
doi: 10.7501/j.issn.0253-2670.2026.06.002
文章导航
目的 研究云南藤黄Garcinia yunnanensis 枝叶醋酸乙酯部位中联苯类化学成分。方法 基于联苯衍生物的紫外光谱特征吸收,综合采用正相硅胶柱、Sephadex LH-20 凝胶柱和半制备HPLC等方法进行目标分离纯化。依据单体化合物的理化性质与波谱数据,并结合相关文献进行结构鉴定。通过抑制一氧化氮生成实验,评价新化合物的抗炎活性。结果 从云南藤黄醋酸乙酯部位中分离得到8个联苯类成分,分别鉴定为 (R )-5-(4-羟基苯基)-2-(2-羟基丙基)-2,3-二氢苯并呋喃-7-醇(1 )、garcibiphenyl C(2 )、cylindrobiphenyl B(3 )、multibiphenyl C(4 )、doitungbiphenyls B(5 )、multiflorabiphenyl B(6 )、和厚朴酚(7 )和厚朴酚(8 )。结论 化合物1 为新化合物,命名为藤黄联苯A(yunnabiphenyl A);化合物2 ~8 均为首次从该植物中分离得到。化合物1 显示一定的抗炎活性,其半数抑制浓度(median inhibition concentration,IC₅₀)为21.5μmol/L。
云南藤黄
/
联苯
/
抗炎
/
藤黄联苯A
/
和厚朴酚
/
厚朴酚
/
garcibiphenyl C
Objective To investigate the biphenyl compounds in the ethyl acetate-soluble fraction of the twigs of Garcinia yunnanensis . Methods Based on the UV spectral characteristics absorption of biphenyl derivatives, targeted separation and purification were performed using various chromatography techniques, including silica gel column chromatography, Sephadex LH-20 gel column and semi-preparative HPLC. The structures of the isolated compounds were elucidated by means of physicochemical properties and spectral data of the monomer compounds, in combination with relevant literature. The anti-inflammatory activity of the new compound was evaluated by measuring its inhibition effect of nitric oxide (NO) production. Results Eight bipheny derivatives were obtained from the ethyl acetate fraction of G. yunnanensis , elucidated as (R )-5-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-2,3-dihydrobenzofuran-7-ol (1 ), garcibiphenyl C (2 ), cylindrobiphenyl B (3 ), multibiphenyl C (4 ), doitungbiphenyls B (5 ), multiflorabiphenyl B (6 ), honokiol (7 ), and magnolol (8 ). Conclusion Compound 1 is a new compound named yunnabiphenyl A, while compounds 2 —8 were reported from this plant for the first time. Compound 1 showed moderate anti-inflammatory activity, with a median inhibition concentration (IC50 ) value of 21.5 μmol/L.
Garcinia yunnanensis H. H. Hu
/
biphenyl
/
anti-inflammatory
/
yunnabiphenyl A
/
honokiol
/
magnolol
/
garcibiphenyl C
余越, 陈煜, 彭财英, 梁永红, 刘建群, 舒积成.
云南藤黄中联苯类成分研究.
中草药,
2026
, 57
(6)
: 2016
-2021
.
DOI: 10.7501/j.issn.0253-2670.2026.06.002
YU Yue, CHEN Yu, PENG Caiying, LIANG Yonghong, LIU Jianqun, SHU Jicheng.
Biphenyl compounds isolated from Garcinia yunnanensis [J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(6)
: 2016
-2021
.
DOI: 10.7501/j.issn.0253-2670.2026.06.002
参考文献
引证文献
中国科学院中国植物志编辑委员会. 中国植物志-第六十九卷[M]. 北京: 科学出版社, 1990: 94. 《全国中草药汇编》编写组. 全国中草药汇编(卷三)[M]. 第3版. 北京: 人民卫生出版社, 2014: 675. Boonyong C, Pattamadilok C, Suttisri R, et al . Benzophenones and xanthone derivatives from Garcinia schomburgkiana -induced P-glycoprotein overexpression in human colorectal Caco-2 cells via oxidative stress-mediated mechanisms[J]. Phytomedicine , 2017, 27: 8-14. Shahid M, Law D, Azfaralariff A, et al . Phytochemicals and biological activities of Garcinia atroviridis : A critical review[J]. Toxics , 2022, 10(11): 656. Rizaldy D, Hartati R, Nadhifa TFI. Chemical compounds and pharmacological activities of Mangosteen (Garcinia mangostana L.)-updated review[J]. Biointerface Res App , 2022, 12(2): 2503-2516. Fu Y G, Huang Y Q, Xu Z H, et al . Polyprenylated acylphloroglucinols from Garcinia species and structural revision of seven analogues[J]. Nat Prod Bioprospect , 2025, 15(1): 34. Lim S H, Lee H S, Lee C H, et al . Pharmacological activity of Garcinia indica (kokum): An updated review[J]. Pharmaceuticals , 2021, 14(12): 1338. Hu X Y, Luo H J, Wei X, et al . Anti-inflammatory bicyclic polyprenylated acylphloroglucinols with diverse architectures including an unprecedented 6/6/6 tricyclic core from Garcinia yunnanensis [J]. Bioorg Chem , 2024, 153: 107864. Nan M M, Yang Y Y, Ying P, et al . Garciyunnanones A-R: Caged polycyclic polyprenylated acylphloroglucinols decorated with a lavandulyl substituent from Garcinia yunnanensis [J]. Phytochemistry , 2024, 224: 114167. Wang S, Liu S Y, Wang S, et al . Garciyndiphenyls a and B, two biphenyl dimers with a caged skeleton from Garcinia yunnanensis [J]. Org Lett , 2025, 27(14): 3800-3805. Chen J J, Peng C F, Huang H Y, et al . Benzopyrans, biphenyls and xanthones from the root of Garcinia linii and their activity against Mycobacterium tuberculosis[J]. Planta Med , 2006, 72(5): 473-477. Mungmee C, Sitthigool S, Buakeaw A, et al . A new biphenyl and other constituents from the wood of Garcinia schomburgkiana [J]. Nat Prod Res , 2013, 27(21): 1949-1955. Li Y K, Wang Z Y, Wu X X, et al . Biphenyl derivatives from the twigs of Garcinia bracteata and their biological activities[J]. Phytochem Lett , 2015, 11: 24-27. Kim C S, Subedi L, Kwon O K, et al . Isolation of bioactive biphenyl compounds from the twigs of Chaenomeles sinensis [J]. Bioorg Med Chem Lett , 2016, 26(2): 351-354. Zheng D, Zhang H, Jiang J M, et al . Prenylated xanthones and biphenyls from Garcinia esculenta with antistaphylococcal activity[J]. Nat Prod Res , 2021, 35(13): 2137-2144. Gao X M, Cui D, Wang S S, et al . New biphenyls from Garcinia lancilimba [J]. Phytochem Lett , 2018, 27: 219-222. Pailee P, Kuhakarn C, Sangsuwan C, et al . Anti-HIV and cytotoxic biphenyls, benzophenones and xanthones from stems, leaves and twigs of Garcinia speciosa [J]. Phytochemistry , 2018, 147: 68-79. Tian D S, Gu W, Wang L P, et al . Cytotoxic and anti-oxidant biphenyl derivatives from the leaves and twigs of Garcinia multiflora [J]. Phytochem Lett , 2017, 19: 132-135. Auranwiwat C, Limtharakul T, Pyne S G, et al . A new xanthone and a biphenyl from the flower and twig extracts of Garcinia mckeaniana [J]. Nat Prod Res , 2021, 35(20): 3404-3409. Chaturonrutsamee S, Kuhakarn C, Surawatanawong P, et al . Polycyclic polyprenylated acylphloroglucinols and biphenyl derivatives from the roots of Garcinia nuntasaenii Ngerns. & Suddee[J]. Phytochemistry , 2018, 146: 63-74. 李圆圆, 卢炜仁, 黄慧莲, 等. 欧洲蕨中8-2' 连接的木脂素类成分研究[J]. 中草药, 2025, 56(21): 7675-7679. Asai T, Luo D, Obara Y, et al . Dihydrobenzofurans as cannabinoid receptor ligands from Cordyceps annullata , an entomopathogenic fungus cultivated in the presence of an HDAC inhibitor[J]. Tetrahedron Lett , 2012, 53(17): 2239-2243. Antus S, Kurtán T, Juhász L, et al . Chiroptical properties of 2, 3-dihydrobenzo[b] furan and chromane chromophores in naturally occurring O -heterocycles[J]. Chirality , 2001, 13(8): 493-506. Chen J J, Peng C F, Huang H Y, et al . Benzopyrans, biphenyls and xanthones from the root of Garcinia linii and their activity against Mycobacterium tuberculosis [J]. Planta Med , 2006, 72(5): 473-477. Sukandar E R, Kaennakam S, Rassamee K, et al . Xanthones and biphenyls from the stems of Garcinia cylindrocarpa and their cytotoxicity[J]. Fitoterapia , 2018, 130: 112-117. Gao X M, Ji B K, Li Y K, et al . New biphenyls from Garcinia multiflora [J]. J Braz Chem Soc , 2015: 27(1): 10-14. Siridechakorn I, Maneerat W, Sripisut T, et al . Biphenyl and xanthone derivatives from the twigs of a Garcinia sp. (Clusiaceae)[J]. Phytochem Lett , 2014, 8: 77-80. Fu W W, Wu M, Zhu L L, et al . Prenylated benzoylphloroglucinols and biphenyl derivatives from the leaves of Garcinia multiflora Champ[J]. RSC Adv , 2015, 5(95): 78259-78267. 邓世明, 程永现, 周俊, 等. 长缘厚朴中的新苯醌及新木脂素类化合物[J]. 云南植物研究, 2001, 23(1): 121-125. Suh W S, Park K J, Kim D H, et al . A biphenyl derivative from the twigs of Chaenomeles speciosa [J]. Bioorg Chem , 2017, 72: 156-160. Phukhatmuen P, Raksat A, Laphookhieo S, et al . Bioassay-guided isolation and identification of antidiabetic compounds from Garcinia cowa leaf extract[J]. Heliyon , 2020, 6(4): e03625. Takaoka S, Nakade K, Fukuyama Y. The first total synthesis and neurotrophic activity of clusiparalicoline A, a prenylated and geranylated biaryl from Clusia paralicola [J]. Tetrahedron Lett , 2002, 43(39): 6919-6923. Zhang X C, Gao R R, Liu Y, et al . Anti-virulence activities of biflavonoids from Mesua ferrea L. flower[J]. Drug Discov Ther , 2019, 13(4): 222-227.
2026年第57卷第6期
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doi: 10.7501/j.issn.0253-2670.2026.06.002
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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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