Article(id=1304388071064101818, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388049975137100, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.11.002, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1774022400000, receivedDateStr=2026-03-21, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788919950499, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788919950499, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788919950499, creator=13701087609, updateTime=1788919950499, updator=13701087609, issue=Issue{id=1304388049975137100, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='11', pageStart='4089', pageEnd='4508', issueExtLink='null', onlineDate='null', pubDate='1781193600000', pubDateStr='2026-06-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788919945471, creator='13701087609', updateTime=1788923432386, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304402675202805770, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388049975137100, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304402675207000075, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388049975137100, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=4096, endPage=4102, ext={EN=ArticleExt(id=1304388071399646141, articleId=1304388071064101818, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Chemical constituents from barks of Spondias pinnata and their anti-inflammatory activities, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the chemical constituents from the ethanol extract of the bark of Spondias pinnata and preliminarily evaluate their anti-inflammatory activity. Methods Various chromatographic techniques were employed to isolate and purify the constituents from the extract. Their structures were elucidated by spectroscopic methods including NMR spectroscopy, as well as GFN2NMR and computational chemistry approaches. The anti-inflammatory activity of the new compound was evaluated using an LPS/IFN-γ-induced MH-S cell inflammation model in vitro . Results Ten compounds were isolated from the ethanol extract of the bark of S. pinnata and identified as (5R ,6S )-6-[(7E ,9R )-9-hydroxy-10-({(15R ,16R )-17-butoxycarbonyl-15,16-dihydroxypropoxy})but-7-en-7-yl]-6-hydroxy-1,1-dimethylcyclohexan-3-one (1 ), ampelopsisionoside (2 ), (2E ,4E ,1'R ,3'S ,5'R ,8'S )-dihydrophaseic acid 3'-O- β-D- glucopyranoside (3 ), N -benzoyl-D- phenylalanine (2R )-2-(benzoylamino)-3-phenylpropyl ester (4 ), isolariciresinol-4-O- β-D- glucopyranoside (5 ), (+)-lyoniresin-4-yl-β-D- glucopyranoside (6 ), demethoxymatteucinol (7 ), 4' -hydroxy-3-O- β-D- glucopyranoside flavone (8 ), (2S )-2-hydroxynaringenin-4'-O- β-D- glucoside (9 ), and (S )-(-)-N -benzoylphenylalaninol (10 ). Compound 1 significantly inhibited the expression of TNF-α (P < 0.05) and IL-6 (P < 0.01) at a concentration of 10 μmol/L. Moreover, at 20 μmol/L, it markedly ameliorated the LPS/IFN-γ-induced morphological changes in MH-S cells. Conclusion Compound 1 is a new compound, named as spondias A. Compounds 2 —4 and 7 —10 were isolated from the genus Spondias for the first time, while compounds 5 —6 were obtained from this species for the first time. The bioassay results indicate that compound 1 inhibits the transformation of MH-S cells to the M1 phenotype, suggesting its potential anti-inflammatory activity., authors=ZHAO Jinna, FU Rong, PIAO Xianmei, WANG Jinhui, WANG Libo, authorsList=ZHAO Jinna, FU Rong, PIAO Xianmei, WANG Jinhui, WANG Libo, 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=1304388071328342972, articleId=1304388071064101818, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=槟榔青树皮中的化学成分及抗炎活性研究, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究槟榔青Spondias pinnata 树皮乙醇提取物中的化学成分,并初步评价其抗炎活性。方法 利用多种色谱技术对提取物进行分离纯化,采用核磁共振等光谱学技术以及GFN2NMR和计算化学等确定化合物的结构。通过体外脂多糖(lipopolysaccharide,LPS)/γ干扰素(interferon gamma,IFN-γ)诱导的MH-S炎症模型考察新化合物的抗炎活性。结果 从槟榔青树皮乙醇提取物中分离得到10个化合物,分别鉴定为 (5R ,6S )-6-[(7E ,9R )-9-hydroxy-10-({(15R ,16R )-17-butoxycarbonyl-15,16-dihydroxypropoxy})but-7-en-7-yl]-6-hydroxy-1,1-dimethyl- cyclohexan-3-one(1 )、ampelopsisionoside(2 )、(2E ,4E ,1¢R ,3¢S , 5¢R ,8¢S )-dihydrophaseic acid 3¢-O- β-D- glucopyranoside(3 )、N -benzoyl-D- phenylalanine (2R )-2-(benzoylamino)-3-phenylpropyl ester(4 )、异落叶松树脂醇-4-O- β-D- 吡喃葡萄糖苷(5 )、(+)-lyoniresin-4-yl-β-D- glucopyranoside(6 )、去甲氧基荚果蕨素(7 )、4¢-羟基-3-O- b-D- 吡喃葡萄糖黄酮苷(8 )、(2S )-2-hydroxynaringenin-4′-O- β-D- glucoside(9 )、(S )-(-)-N -苯甲酰苯丙氨醇(10 )。化合物1 在10 μmol/L浓度下显著抑制肿瘤坏死因子(tumor necrosis factor-α,TNF-α)(P <0.05)和白细胞介素-6(interleukin-6,IL-6)(P <0.01)的表达。在20 μmol/L浓度下其能显著改善LPS/IFN-γ诱导的MH-S细胞形态变化。结论 化合物1 为新化合物,命名为槟榔青素A(spondias A);化合物2 ~4 、7 ~10 为首次从该属中分离得到,化合物5 ~6 为首次从该植物中分离得到。活性实验结果表明化合物1 可抑制MH-S细胞向M1表型转化,具有潜在的抗炎活性。, authors=赵晋娜1 , 付嵘1 , 朴贤美2 , 王金辉1 , 王立波1 , authorsList=赵晋娜, 付嵘, 朴贤美, 王金辉, 王立波, authorCompany=1 哈尔滨医科大学药学院 药物化学与天然药物化学教研室, 黑龙江 哈尔滨 150081; 2 哈尔滨医科大学药学院药理学教研室, 黑龙江 哈尔滨 150081, correspAuthors=王金辉, authorNote=赵晋娜: 赵晋娜,女,博士研究生,研究方向为天然药物化学。E-mail:jinna0902@163.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=0Fg+KxgLXZeBxwi1XwEyfw==, pdfFileSize=911687, 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=国家自然科学基金项目 (81202418); 黑龙江省中医药管理局科研项目 (ZHY2024-134))}, authors=null, keywords=[Keyword(id=1304401310074298522, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388071064101818, language=CN, orderNo=1, keyword=槟榔青), Keyword(id=1304401310258847899, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388071064101818, language=CN, orderNo=2, keyword=抗炎活性), Keyword(id=1304401310397259932, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388071064101818, language=CN, orderNo=3, keyword=槟榔青素A), Keyword(id=1304401310535671965, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388071064101818, language=CN, orderNo=4, keyword=去甲氧基荚果蕨素), Keyword(id=1304401310644723870, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388071064101818, language=CN, orderNo=5, keyword=4¢), Keyword(id=1304401310892187807, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388071064101818, language=CN, orderNo=6, keyword=-羟基-3-O- b-D- 吡喃葡萄糖黄酮苷), Keyword(id=1304401311009628320, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388071064101818, language=CN, orderNo=7, keyword=(S )-(-)-N -苯甲酰苯丙氨醇), Keyword(id=1304401312913842337, tenantId=1146029695717560320, journalId=1302319053441957962, articleId=1304388071064101818, language=EN, orderNo=1, keyword=Spondias pinnata (L. f.) 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submissionFirstDecision=null, sciSubjectClassification=null, casSubjectClassification=null, citeScore=null, totalCitationFrequency=null, icpCode=null, psCode=null, advertisingLicenseCode=null, copyrightInformation=null, country=null, option=, provinceCode=null, provinceName=null, collectFlag=false, interPubPlatform=, interPubPlatformUrl=null), detailUrlCn=https://castjournals.cast.org.cn/joweb/zcy/CN/10.7501/j.issn.0253-2670.2026.11.002, detailUrlEn=https://castjournals.cast.org.cn/joweb/zcy/EN/10.7501/j.issn.0253-2670.2026.11.002, pdfUrlCn=https://castjournals.cast.org.cn/joweb/zcy/CN/PDF/10.7501/j.issn.0253-2670.2026.11.002, pdfUrlEn=https://castjournals.cast.org.cn/joweb/zcy/EN/PDF/10.7501/j.issn.0253-2670.2026.11.002, aliStartDate=null, aliEndDate=null, collectionFlag=false, citedCount=null, citedUrl=null, previewStatus=0, delFlag=0, hasFullText=0, orderTime=1788919950499, fullTextJson=null, articleText=null, reference=马洁, 管艳红, 张丽霞. 槟榔青的应用价值[J]. 时珍国医国药, 2004, 15(10): 727. Ghate N B, Hazra B, Sarkar R, et al. In vitro anticancer activity of Spondias pinnata bark on human lung and breast carcinoma [J]. Cytotechnology, 2014, 66(2): 209-218. Chalise J P, Acharya K, Gurung N, et al. Antioxidant activity and polyphenol content in edible wild fruits from Nepal [J]. Int J Food Sci Nutr, 2010, 61(4): 425-432. Rao B G, RaJu N J. Investigation of hepatoprotective activity of Spondias pinnata [J]. Int. J. Pharm. Sci. Res, 2010, 1(3): 193-198. Li R, Yang J J, Song X Z, et al. Chemical composition and the cytotoxic, antimicrobial, and anti-inflammatory activities of the fruit peel essential oil from Spondias pinnata (Anacardiaceae) in Xishuangbanna, southwest China [J]. Molecules, 2020, 25(2): 343. Pereira C, de Oliveira L L, Gonçalves R, et al. Phytochemical and phylogenetic analysis of Spondias (Anacardiaceae) [J]. Química N, 2015, 38(6): 813-816. Tandon S, Rastogi R. Studies on the chemical constituents of Spondias Pinnata [J]. Planta Med, 1976, 29(2): 190-192. Elufioye T, Obuotor E, Agbedahunsi J, et al. Anticholinesterase constituents from the leaves of Spondias mombin L. (Anacardiaceae) [J]. Biol Targets Ther, 2017, 11: 107-114. De Marino S, Borbone N, Zollo F, et al. Megastigmane and phenolic components from Laurus nobilis L. leaves and their inhibitory effects on nitric oxide production [J]. J Agric Food Chem, 2004, 52(25): 7525-7531. Ai W J, Li J, Cao D S, et al. A very deep graph convolutional network for 13 NMR chemical shift calculations with density functional theory level performance for structure assignment [J]. J Nat Prod, 2024, 87(4): 743-752. 蓝鸣生, 马健雄, 谭昌恒, 等. 红鱼眼化学成分研究[J]. 中草药, 2011, 42(9): 1712-1714. Catalán C A N, de Heluani C S, Kotowicz C, et al. A linear sesterterpene, two squalene derivatives and two peptide derivatives from Croton hieronymi [J]. Phytochemistry, 2003, 64(2): 625-629. 石舒雅. 宽叶打碗花化学成分及其降糖活性初步研究[D]. 广州: 广东药科大学, 2019. Jin H G, Kim A R, Ko H J, et al. A new megastigmane glycoside from Akebia quinata [J]. Arch Pharmacal Res, 2015, 38(5): 591-597. 吴泳樟, 张玉波, 陈能花, 等. 洋蒲桃枝叶化学成分研究[J]. 中药材, 2015, 38(4): 754-757. Lee S G, Karadeniz F, Seo Y, et al. Anti-melanogenic effects of flavonoid glycosides from Limonium tetragonum (Thunb.) Bullock via inhibition of tyrosinase and tyrosinase-related proteins [J]. Molecules, 2017, 22(9): 1480. 曾鹏, 张勇, 潘晨, 等. 巴东过路黄酚类化学成分研究[J]. 药学学报, 2013, 48(3): 377-382. 南彩云, 朱继孝, 蒋伟, 等. 滇结香花的化学成分研究[J]. 中药材, 2017, 40(7): 1618-1621.)
中草药
|化学成分
2026
, 57
(11) :
4096
-4102
槟榔青树皮中的化学成分及抗炎活性研究
全屏
赵晋娜1 , 付嵘1 , 朴贤美2 , 王金辉1 , 王立波1
作者信息
1 哈尔滨医科大学药学院 药物化学与天然药物化学教研室, 黑龙江 哈尔滨 150081; 2 哈尔滨医科大学药学院药理学教研室, 黑龙江 哈尔滨 150081
通讯作者:
王金辉
作者简介:
赵晋娜: 赵晋娜,女,博士研究生,研究方向为天然药物化学。E-mail:jinna0902@163.com
Chemical constituents from barks of Spondias pinnata and their anti-inflammatory activities
ZHAO Jinna, FU Rong, PIAO Xianmei, WANG Jinhui, WANG Libo
Affiliations
doi: 10.7501/j.issn.0253-2670.2026.11.002
文章导航
目的 研究槟榔青Spondias pinnata 树皮乙醇提取物中的化学成分,并初步评价其抗炎活性。方法 利用多种色谱技术对提取物进行分离纯化,采用核磁共振等光谱学技术以及GFN2NMR和计算化学等确定化合物的结构。通过体外脂多糖(lipopolysaccharide,LPS)/γ干扰素(interferon gamma,IFN-γ)诱导的MH-S炎症模型考察新化合物的抗炎活性。结果 从槟榔青树皮乙醇提取物中分离得到10个化合物,分别鉴定为 (5R ,6S )-6-[(7E ,9R )-9-hydroxy-10-({(15R ,16R )-17-butoxycarbonyl-15,16-dihydroxypropoxy})but-7-en-7-yl]-6-hydroxy-1,1-dimethyl- cyclohexan-3-one(1 )、ampelopsisionoside(2 )、(2E ,4E ,1¢R ,3¢S , 5¢R ,8¢S )-dihydrophaseic acid 3¢-O- β-D- glucopyranoside(3 )、N -benzoyl-D- phenylalanine (2R )-2-(benzoylamino)-3-phenylpropyl ester(4 )、异落叶松树脂醇-4-O- β-D- 吡喃葡萄糖苷(5 )、(+)-lyoniresin-4-yl-β-D- glucopyranoside(6 )、去甲氧基荚果蕨素(7 )、4¢-羟基-3-O- b-D- 吡喃葡萄糖黄酮苷(8 )、(2S )-2-hydroxynaringenin-4′-O- β-D- glucoside(9 )、(S )-(-)-N -苯甲酰苯丙氨醇(10 )。化合物1 在10 μmol/L浓度下显著抑制肿瘤坏死因子(tumor necrosis factor-α,TNF-α)(P <0.05)和白细胞介素-6(interleukin-6,IL-6)(P <0.01)的表达。在20 μmol/L浓度下其能显著改善LPS/IFN-γ诱导的MH-S细胞形态变化。结论 化合物1 为新化合物,命名为槟榔青素A(spondias A);化合物2 ~4 、7 ~10 为首次从该属中分离得到,化合物5 ~6 为首次从该植物中分离得到。活性实验结果表明化合物1 可抑制MH-S细胞向M1表型转化,具有潜在的抗炎活性。
槟榔青
/
抗炎活性
/
槟榔青素A
/
去甲氧基荚果蕨素
/
4¢
/
-羟基-3-O- b-D- 吡喃葡萄糖黄酮苷
/
(S )-(-)-N -苯甲酰苯丙氨醇
Objective To investigate the chemical constituents from the ethanol extract of the bark of Spondias pinnata and preliminarily evaluate their anti-inflammatory activity. Methods Various chromatographic techniques were employed to isolate and purify the constituents from the extract. Their structures were elucidated by spectroscopic methods including NMR spectroscopy, as well as GFN2NMR and computational chemistry approaches. The anti-inflammatory activity of the new compound was evaluated using an LPS/IFN-γ-induced MH-S cell inflammation model in vitro . Results Ten compounds were isolated from the ethanol extract of the bark of S. pinnata and identified as (5R ,6S )-6-[(7E ,9R )-9-hydroxy-10-({(15R ,16R )-17-butoxycarbonyl-15,16-dihydroxypropoxy})but-7-en-7-yl]-6-hydroxy-1,1-dimethylcyclohexan-3-one (1 ), ampelopsisionoside (2 ), (2E ,4E ,1'R ,3'S ,5'R ,8'S )-dihydrophaseic acid 3'-O- β-D- glucopyranoside (3 ), N -benzoyl-D- phenylalanine (2R )-2-(benzoylamino)-3-phenylpropyl ester (4 ), isolariciresinol-4-O- β-D- glucopyranoside (5 ), (+)-lyoniresin-4-yl-β-D- glucopyranoside (6 ), demethoxymatteucinol (7 ), 4' -hydroxy-3-O- β-D- glucopyranoside flavone (8 ), (2S )-2-hydroxynaringenin-4'-O- β-D- glucoside (9 ), and (S )-(-)-N -benzoylphenylalaninol (10 ). Compound 1 significantly inhibited the expression of TNF-α (P < 0.05) and IL-6 (P < 0.01) at a concentration of 10 μmol/L. Moreover, at 20 μmol/L, it markedly ameliorated the LPS/IFN-γ-induced morphological changes in MH-S cells. Conclusion Compound 1 is a new compound, named as spondias A. Compounds 2 —4 and 7 —10 were isolated from the genus Spondias for the first time, while compounds 5 —6 were obtained from this species for the first time. The bioassay results indicate that compound 1 inhibits the transformation of MH-S cells to the M1 phenotype, suggesting its potential anti-inflammatory activity.
Spondias pinnata (L. f.) Kurz.
/
anti-inflammatory activity
/
spondias A
/
demethoxymatteucinol
/
4' -hydroxy-3-O- β-D- glucopyranoside flavone
/
(S )-(-)-N -benzoylphenylalaninol
赵晋娜, 付嵘, 朴贤美, 王金辉, 王立波.
槟榔青树皮中的化学成分及抗炎活性研究.
中草药,
2026
, 57
(11)
: 4096
-4102
.
DOI: 10.7501/j.issn.0253-2670.2026.11.002
ZHAO Jinna, FU Rong, PIAO Xianmei, WANG Jinhui, WANG Libo.
Chemical constituents from barks of Spondias pinnata and their anti-inflammatory activities[J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(11)
: 4096
-4102
.
DOI: 10.7501/j.issn.0253-2670.2026.11.002
参考文献
引证文献
马洁, 管艳红, 张丽霞. 槟榔青的应用价值[J]. 时珍国医国药, 2004, 15(10): 727. Ghate N B, Hazra B, Sarkar R, et al. In vitro anticancer activity of Spondias pinnata bark on human lung and breast carcinoma [J]. Cytotechnology, 2014, 66(2): 209-218. Chalise J P, Acharya K, Gurung N, et al. Antioxidant activity and polyphenol content in edible wild fruits from Nepal [J]. Int J Food Sci Nutr, 2010, 61(4): 425-432. Rao B G, RaJu N J. Investigation of hepatoprotective activity of Spondias pinnata [J]. Int. J. Pharm. Sci. Res, 2010, 1(3): 193-198. Li R, Yang J J, Song X Z, et al. Chemical composition and the cytotoxic, antimicrobial, and anti-inflammatory activities of the fruit peel essential oil from Spondias pinnata (Anacardiaceae) in Xishuangbanna, southwest China [J]. Molecules, 2020, 25(2): 343. Pereira C, de Oliveira L L, Gonçalves R, et al. Phytochemical and phylogenetic analysis of Spondias (Anacardiaceae) [J]. Química N, 2015, 38(6): 813-816. Tandon S, Rastogi R. Studies on the chemical constituents of Spondias Pinnata [J]. Planta Med, 1976, 29(2): 190-192. Elufioye T, Obuotor E, Agbedahunsi J, et al. Anticholinesterase constituents from the leaves of Spondias mombin L. (Anacardiaceae) [J]. Biol Targets Ther, 2017, 11: 107-114. De Marino S, Borbone N, Zollo F, et al. Megastigmane and phenolic components from Laurus nobilis L. leaves and their inhibitory effects on nitric oxide production [J]. J Agric Food Chem, 2004, 52(25): 7525-7531. Ai W J, Li J, Cao D S, et al. A very deep graph convolutional network for 13 NMR chemical shift calculations with density functional theory level performance for structure assignment [J]. J Nat Prod, 2024, 87(4): 743-752. 蓝鸣生, 马健雄, 谭昌恒, 等. 红鱼眼化学成分研究[J]. 中草药, 2011, 42(9): 1712-1714. Catalán C A N, de Heluani C S, Kotowicz C, et al. A linear sesterterpene, two squalene derivatives and two peptide derivatives from Croton hieronymi [J]. Phytochemistry, 2003, 64(2): 625-629. 石舒雅. 宽叶打碗花化学成分及其降糖活性初步研究[D]. 广州: 广东药科大学, 2019. Jin H G, Kim A R, Ko H J, et al. A new megastigmane glycoside from Akebia quinata [J]. Arch Pharmacal Res, 2015, 38(5): 591-597. 吴泳樟, 张玉波, 陈能花, 等. 洋蒲桃枝叶化学成分研究[J]. 中药材, 2015, 38(4): 754-757. Lee S G, Karadeniz F, Seo Y, et al. Anti-melanogenic effects of flavonoid glycosides from Limonium tetragonum (Thunb.) Bullock via inhibition of tyrosinase and tyrosinase-related proteins [J]. Molecules, 2017, 22(9): 1480. 曾鹏, 张勇, 潘晨, 等. 巴东过路黄酚类化学成分研究[J]. 药学学报, 2013, 48(3): 377-382. 南彩云, 朱继孝, 蒋伟, 等. 滇结香花的化学成分研究[J]. 中药材, 2017, 40(7): 1618-1621.
2026年第57卷第11期
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doi: 10.7501/j.issn.0253-2670.2026.11.002
接收时间:2026-03-21
首发时间:2026-09-09
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2种不同金属材料的力学参数
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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