Article(id=1304388180749345268, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388157621948709, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.15.001, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1778515200000, receivedDateStr=2026-05-12, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788919976650, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788919976650, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788919976650, creator=13701087609, updateTime=1788919976650, updator=13701087609, issue=Issue{id=1304388157621948709, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='15', pageStart='5789', pageEnd='6208', issueExtLink='null', onlineDate='null', pubDate='1786464000000', pubDateStr='2026-08-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=1, specialIssue=null, createTime=1788919971137, creator='13701087609', updateTime=1788923514106, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304403017982300207, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388157621948709, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304403017982300208, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304388157621948709, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=5789, endPage=5798, ext={EN=ArticleExt(id=1304388181055529462, articleId=1304388180749345268, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=A new labdane-type diterpenoid from branches and leaves of Aphanamixis polystachya , columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To study chemical constituents and neuroprotective activities of the branches and leaves of Aphanamixis polystachya . Methods Monomer compounds were obtained through separation and purification using various chromatographic techniques including silica gel column chromatography, reversed-phase ODS column, Sephadex LH-20, semi-preparative HPLC, and recrystallization. Their structures were elucidated by modern spectroscopic methods including nuclear magnetic resonance (NMR), high-resolution electrospray ionization mass spectrometry (HRESIMS), infrared spectroscopy (IR), ultraviolet spectroscopy (UV), and single-crystal X-ray diffraction analysis. Results A total of 21 compounds were isolated from the branches and leaves of A. polystachya , identified as, (2R ,5R ,8S ,9S ,10R )-1-[(E )-5-hydroxy-3-methylpent-3-en-1-yl]-4,4,8,10-tetramethyldecahydronaphthalene-2,8-diol (1 ), (1S ,4aS ,7R ,8R ,8aS )-decahydro-8-[(3E )-5-hydroxy-3-methyl-3-penten-1-yl]-4,4,7,8a-tetramethyl-1,7-naphthalenediol (2 ), 3β,8α,15-trihydroxy-13-labdane (3 ), 8β,15-dihydroxy-ent-labda-13E -en-3-one (4 ), labd-13(E )-ene-8α,15-diol (5 ), labd-13(E )-ene-8α-hydroxy-15-acetate (6 ), labda-7,13E -dien-15-ol (7 ), labda-8,13E -dien-15-ol (8 ), brachytylin D (9 ), labda-8(17),13E -dien-15-ol (10 ), selin-11-en-4α-ol (11 ), (±)-selin-11-en-4α-ol (12 ), (1S ,5R ,9R )-10,10-dimethyl-2,6-dimethylenebicyclo[7.2.0]undecane-5-ol (13 ), caryophyllenol-II (14 ), ciwujiatone (15 ), lyoniresinol (16 ), isolariciresinol (17 ), (±)-ficusesquilignan A (18 ), ficusesquilignan B (19 ), syringaresinol (20 ), methyl rosmarinate (21 ). Conclusion Compound 1 is a novel compound designated as labdane diterpenoid Z. Compounds 2 -4 , 9 , 11 -15 , and 18 -21 are isolated from genus Aphanamixis for the first time, which further enriches the chemical component database of the genus Aphanamixis . Furthermore, biological activity assays reveals that compound 21 exhibits neuroprotective activity., authors=SUN Chuxiang, PU Wanjun, LI Jinyu, LIU Hanfei, ZHANG Ni, PAN Weidong, authorsList=SUN Chuxiang, PU Wanjun, LI Jinyu, LIU Hanfei, ZHANG Ni, PAN Weidong, 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=1304388180980031989, articleId=1304388180749345268, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=山楝枝叶中1个新的半日花烷型二萜, columnId=1304140187169214944, journalTitle=中草药, columnName=化学成分, runingTitle=null, highlight=null, articleAbstract=目的 研究山楝Aphanamixis polystachya 枝叶的化学成分及神经保护活性。方法 利用硅胶、反相ODS、葡聚糖凝胶(Sephadex LH-20)、半制备型HPLC、重结晶等多种技术进行分离纯化,得到单体化合物。综合使用核磁共振波谱(NMR)、高分辨质谱(HRESIMS)、红外光谱(IR)、紫外光谱(UV)、X-ray单晶衍射等现代分析手段对单体化合物进行结构鉴定。结果 从山楝枝叶90%乙醇提取物中分离得到21个化合物,分别鉴定为 (2R ,5R ,8S ,9S ,10R )-1-[(E )-5-hydroxy-3-methylpent-3-en-1-yl]-4,4,8,10-tetramethyldecahydronaphthalene-2,8-diol(1 )、(1S ,4aS ,7R ,8R ,8aS )-十氢-8-[(3E )-5-羟基-3-甲基-3-戊烯-1-基]-4,4,7,8a-四甲基-1,7-萘二醇(2 )、3β,8α,15-三羟基-13-半日花烷(3 )、8β,15-二羟基-对映-13E -半日花烯-3-酮(4 )、13E -半日花烯-8α,15-二醇(5 )、13E -半日花烯-8α-羟基-15-乙酸酯(6 )、7,13E -半日花二烯-15-醇(7 )、8,13E -半日花二烯-15-醇(8 )、brachytylin D(9 )、labda-8(17),13E -dien-15-ol(10 )、α-网翼藻萜醇(11 )、(±)-selin-11-en-4α-ol(12 )、(1S ,5R ,9R )-10,10-dimethyl-2,6-dimethylenebicyclo[7.2.0]undecane-5-ol(13 )、石竹烯醇-II(14 )、刺五加酮(15 )、南烛木树脂酚(16 )、异落叶松脂素(17 )、(±)-ficusesquilignan A(18 )、ficusesquilignan B(19 )、丁香脂素(20 )、迷迭香酸甲酯(21 )。结论 化合物1 为新化合物,命名为半日花烷型二萜Z。化合物2 ~4 、9 、11 ~15 、18 ~21 均为首次从山楝属植物中分离得到,该研究进一步丰富了山楝属植物的化学成分数据库,且生物活性研究发现化合物21 具有神经保护活性。, authors=孙出香1,2 , 蒲婉君2 , 李金玉2,3 , 刘翰飞2,3 , 张妮2,3 , 潘卫东2,3 , authorsList=孙出香, 蒲婉君, 李金玉, 刘翰飞, 张妮, 潘卫东, authorCompany=1 贵州中医药大学, 贵州 贵阳 550025; 2 贵州医科大学中药功效成分发掘与利用全国重点实验室, 贵州 贵阳 550014; 3 贵州省天然产物研究中心, 贵州 贵阳 550014, correspAuthors=张妮, authorNote=孙出香: 孙出香,女,硕士研究生,研究方向为天然药物化学。E-mail:2649842443@qq.com
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Inhibitory effects of phenolic compounds from needles of Pinus densiflora on nitric oxide and PGE2 production [J]. Arch Pharmacal Res, 2010, 33(12): 2011-2016. Wen L R, You L J, Yang X M, et al. Identification of phenolics in Litchi and evaluation of anticancer cell proliferation activity and intracellular antioxidant activity [J]. Free Radic Biol Med, 2015, 84: 171-184. Mahmoud B K, Samy M N, Hamed A N E, et al. Bignanoside A “a new neolignan glucoside” and bignanoside B “a new iridoid glucoside” from Bignonia binata leaves [J]. Phytochem Lett, 2020, 35: 200-205. Zhang Y, Wang J S, Gu Y C, et al. Diverse prieurianin-type limonoid derivatives from the fruits of Aphanamixis grandifolia and their absolute configuration determination [J]. Tetrahedron, 2014, 70(37): 6594-6606. Zhang Y, Wang J S, Luo J, et al. Novel nortriterpenoids from Aphanamixis grandifolia [J]. Chem Pharm Bull, 2011, 59(2): 282-286. Wang X B, Zhang Y, Wang J S, et al. Novel ring A rearranged isomers with γ-lactone from the fruits of Aphanamixis grandifolia [J]. Tetrahedron Lett, 2013, 54(45): 6023-6028. Chen Y W, Wu S L, Dong F W, et al. Four new tirucallane-type triterpenoids from Aphanamixis polystachya [J]. J Asian Nat Prod Res, 2024, 26(8): 883-891. Zeng Q, Guan B, Qin J J, et al. 2,3-Seco- and 3,4-seco-tirucallane triterpenoid derivatives from the stems of Aphanamixis grandifolia Blume [J]. Phytochemistry, 2012, 80: 148-155. Zeng Q, Guan B, Ren J, et al. Aphanamgrandiol A, a new triterpenoid with a unique carbon skeleton from Aphanamixis grandifolia [J]. Fitoterapia, 2013, 86: 217-221. Wang X Y, Tang G H, Yuan C M, et al. Two new tirucallane triterpenoids from Aphanamixis grandifolia [J]. Nat Prod Bioprospect, 2012, 2(5): 222-226. Yang X, Wu S L, Li B J, et al. Triterpenoids from the fruits of Aphanamixis polystachya and their inhibitory activities on nitric oxide production [J]. Fitoterapia, 2023, 171: 105709. Wang D T, Xue Y Y, Zhang Y F, et al. Lignans and phenylpropanoids from the liquid juice of Phyllostachys edulis [J]. Nat Prod Res, 2021, 35(19): 3241-3247. Liao S G, Yuan T, Zhang C, et al. Cinnacassides A–E, five geranylphenylacetate glycosides from Cinnamomum Cassia [J]. Tetrahedron, 2009, 65(4): 883-887. Dagne E, Bisrat D, Van Wyk B E, et al. 10-Hydroxyaloin B 6'-O-acetate, an oxanthrone from Aloe claviflora [J]. J Nat Prod, 1998, 61(2): 256-257. Forster P G, Ghisalberti E L, Jefferies P R. Labdane diterpenes from an Acacia species [J]. Phytochemistry, 1985, 24(12): 2991-2993. Koukoulitsa C, Zervou M, Demetzos C, et al. Comparative docking studies of labdane-type diterpenes with forskolin at the active site of adenylyl cyclase [J]. Bioorg Med Chem, 2008, 16(17): 8237-8243. Zdero C, Bohlmann F, Niemeyer H M. Seco-labdanes and other constituents from Ophryosporus floribundus [J]. Phytochemistry, 1990, 29(10): 3247-3253. Koukoulitsa C, Zervou M, Demetzos C, et al. Comparative docking studies of labdane-type diterpenes with forskolin at the active site of adenylyl cyclase [J]. Bioorg Med Chem, 2008, 16(17): 8237-8243. 秦天丽, 陈彦伍, 吴石丽, 等. 山楝枝叶中两个新的倍半萜[J]. 天然产物研究与开发, 2021, 33(2): 222-226. 张勇, 石倪霏, 谢珍, 等. 黄牛木枝叶中化学成分及其抑制滑膜成纤维细胞增殖活性研究[J]. 中国中药杂志, 2023, 48(18): 5014-5023. Lago J H G, Brochini C B, Roque N F. Terpenes from leaves of Guarea macrophylla (Meliaceae) [J]. Phytochemistry, 2000, 55(7): 727-731. Jiang W, Xiong J, Zang Y, et al. Phytochemical and biological studies on rare and endangered plants endemic to China. Part XIV. Structurally diverse terpenoids from the twigs and needles of the endangered plant Picea brachytyla [J]. Phytochemistry, 2020, 169: 112161. 陈彦伍, 秦天丽, 吴石丽, 等. 华山楝枝叶的化学成分及抗菌活性研究[J]. 中草药, 2020, 51(18): 4614-4619. Taber D F, Bhamidipati R S, Yet L. Phenyldimethylsilyl as an alcohol surrogate in intramolecular Diels-Alder cycloaddition: Synthesis of alpha-dictyopterol [J]. J Org Chem, 1995, 60(17): 5537-5539. Waβmuth-Wagner I, Kalinowski H O, Jork H. Isolation and identification of 11-selinen-4α, 7β-ol and 10-aromadendranol in the essential oil of Murraya koenigii [J]. Planta Med, 1995, 61(2): 196-197. Stakanovs G, Blazevica A, Belyakov S, et al. Semisynthesis of linariophyllenes A–C and rumphellolide H, structure revisions and proposed biosynthesis pathways [J]. J Nat Prod, 2023, 86(10): 2368-2378. Izdihar G, Naini A A, Harneti D, et al. Sesquiterpenoids from the stem bark of Aglaia simplicifolia and their cytotoxic activity against B16-F10 melanoma skin cancer cell [J]. Indones J Chem, 2021, 21(6): 1560. 贾自立, 田文静, 杨任靖, 等. 仙鹤草中木脂素类成分的研究[J]. 中国中药杂志, 2022, 47(11): 2982-2988. 黎灵. 细叶勾儿茶的化学成分研究[D]. 遵义: 遵义医科大学, 2025. Jutiviboonsuk A, Zhang H J, Tan G T, et al. Bioactive constituents from roots of Bursera tonkinensis [J]. Phytochemistry, 2005, 66(23): 2745-2751. 丁雯倩, 史国茹, 庾石山. 龙牙花根中化学成分的研究[J]. 中国中药杂志, 2019, 44(14): 3064-3069. Lu Q R, Wang Y, Tang Z Y, et al. Chemical constituents of Wikstroemia alternifolia and their neuroprotective activities [J]. Nat Prod Res, 2024, 38(6): 986-993. 麦德尚, 陈采欣, 曹嘉敏, 等. 佛手的化学成分研究[J]. 中草药, 2025, 56(2): 421-429. Aung H T, Nikai T, Niwa M, et al. Rosmarinic acid in Argusia argentea inhibits snake venom-induced hemorrhage [J]. J Nat Med, 2010, 64(4): 482-486.)
中草药
|化学成分
2026
, 57
(15) :
5789
-5798
山楝枝叶中1个新的半日花烷型二萜
全屏
孙出香1,2 , 蒲婉君2 , 李金玉2,3 , 刘翰飞2,3 , 张妮2,3 , 潘卫东2,3
作者信息
1 贵州中医药大学, 贵州 贵阳 550025; 2 贵州医科大学中药功效成分发掘与利用全国重点实验室, 贵州 贵阳 550014; 3 贵州省天然产物研究中心, 贵州 贵阳 550014
通讯作者:
张妮
作者简介:
孙出香: 孙出香,女,硕士研究生,研究方向为天然药物化学。E-mail:2649842443@qq.com
蒲婉君: 蒲婉君,女,硕士研究生,研究方向为天然药物化学。E-mail:puwanjun1008@163.com
A new labdane-type diterpenoid from branches and leaves of Aphanamixis polystachya
SUN Chuxiang, PU Wanjun, LI Jinyu, LIU Hanfei, ZHANG Ni, PAN Weidong
Affiliations
doi: 10.7501/j.issn.0253-2670.2026.15.001
文章导航
目的 研究山楝Aphanamixis polystachya 枝叶的化学成分及神经保护活性。方法 利用硅胶、反相ODS、葡聚糖凝胶(Sephadex LH-20)、半制备型HPLC、重结晶等多种技术进行分离纯化,得到单体化合物。综合使用核磁共振波谱(NMR)、高分辨质谱(HRESIMS)、红外光谱(IR)、紫外光谱(UV)、X-ray单晶衍射等现代分析手段对单体化合物进行结构鉴定。结果 从山楝枝叶90%乙醇提取物中分离得到21个化合物,分别鉴定为 (2R ,5R ,8S ,9S ,10R )-1-[(E )-5-hydroxy-3-methylpent-3-en-1-yl]-4,4,8,10-tetramethyldecahydronaphthalene-2,8-diol(1 )、(1S ,4aS ,7R ,8R ,8aS )-十氢-8-[(3E )-5-羟基-3-甲基-3-戊烯-1-基]-4,4,7,8a-四甲基-1,7-萘二醇(2 )、3β,8α,15-三羟基-13-半日花烷(3 )、8β,15-二羟基-对映-13E -半日花烯-3-酮(4 )、13E -半日花烯-8α,15-二醇(5 )、13E -半日花烯-8α-羟基-15-乙酸酯(6 )、7,13E -半日花二烯-15-醇(7 )、8,13E -半日花二烯-15-醇(8 )、brachytylin D(9 )、labda-8(17),13E -dien-15-ol(10 )、α-网翼藻萜醇(11 )、(±)-selin-11-en-4α-ol(12 )、(1S ,5R ,9R )-10,10-dimethyl-2,6-dimethylenebicyclo[7.2.0]undecane-5-ol(13 )、石竹烯醇-II(14 )、刺五加酮(15 )、南烛木树脂酚(16 )、异落叶松脂素(17 )、(±)-ficusesquilignan A(18 )、ficusesquilignan B(19 )、丁香脂素(20 )、迷迭香酸甲酯(21 )。结论 化合物1 为新化合物,命名为半日花烷型二萜Z。化合物2 ~4 、9 、11 ~15 、18 ~21 均为首次从山楝属植物中分离得到,该研究进一步丰富了山楝属植物的化学成分数据库,且生物活性研究发现化合物21 具有神经保护活性。
山楝枝叶
/
半日花烷型二萜Z
/
迷迭香酸甲酯
/
石竹烯醇-II
/
刺五加酮
/
神经保护活性
Objective To study chemical constituents and neuroprotective activities of the branches and leaves of Aphanamixis polystachya . Methods Monomer compounds were obtained through separation and purification using various chromatographic techniques including silica gel column chromatography, reversed-phase ODS column, Sephadex LH-20, semi-preparative HPLC, and recrystallization. Their structures were elucidated by modern spectroscopic methods including nuclear magnetic resonance (NMR), high-resolution electrospray ionization mass spectrometry (HRESIMS), infrared spectroscopy (IR), ultraviolet spectroscopy (UV), and single-crystal X-ray diffraction analysis. Results A total of 21 compounds were isolated from the branches and leaves of A. polystachya , identified as, (2R ,5R ,8S ,9S ,10R )-1-[(E )-5-hydroxy-3-methylpent-3-en-1-yl]-4,4,8,10-tetramethyldecahydronaphthalene-2,8-diol (1 ), (1S ,4aS ,7R ,8R ,8aS )-decahydro-8-[(3E )-5-hydroxy-3-methyl-3-penten-1-yl]-4,4,7,8a-tetramethyl-1,7-naphthalenediol (2 ), 3β,8α,15-trihydroxy-13-labdane (3 ), 8β,15-dihydroxy-ent-labda-13E -en-3-one (4 ), labd-13(E )-ene-8α,15-diol (5 ), labd-13(E )-ene-8α-hydroxy-15-acetate (6 ), labda-7,13E -dien-15-ol (7 ), labda-8,13E -dien-15-ol (8 ), brachytylin D (9 ), labda-8(17),13E -dien-15-ol (10 ), selin-11-en-4α-ol (11 ), (±)-selin-11-en-4α-ol (12 ), (1S ,5R ,9R )-10,10-dimethyl-2,6-dimethylenebicyclo[7.2.0]undecane-5-ol (13 ), caryophyllenol-II (14 ), ciwujiatone (15 ), lyoniresinol (16 ), isolariciresinol (17 ), (±)-ficusesquilignan A (18 ), ficusesquilignan B (19 ), syringaresinol (20 ), methyl rosmarinate (21 ). Conclusion Compound 1 is a novel compound designated as labdane diterpenoid Z. Compounds 2 -4 , 9 , 11 -15 , and 18 -21 are isolated from genus Aphanamixis for the first time, which further enriches the chemical component database of the genus Aphanamixis . Furthermore, biological activity assays reveals that compound 21 exhibits neuroprotective activity.
branches and leaves of Aphanamixis polystachya (Wall.) R. N. Parker
/
labdane diterpenoid Z
/
methyl rosmarinate
/
caryophyllenol-II
/
ciwujiatone
/
neuroprotective activity
孙出香, 蒲婉君, 李金玉, 刘翰飞, 张妮, 潘卫东.
山楝枝叶中1个新的半日花烷型二萜.
中草药,
2026
, 57
(15)
: 5789
-5798
.
DOI: 10.7501/j.issn.0253-2670.2026.15.001
SUN Chuxiang, PU Wanjun, LI Jinyu, LIU Hanfei, ZHANG Ni, PAN Weidong.
A new labdane-type diterpenoid from branches and leaves of Aphanamixis polystachya [J].
Chinese Traditional and Herbal Drugs ,
2026
, 57
(15)
: 5789
-5798
.
DOI: 10.7501/j.issn.0253-2670.2026.15.001
参考文献
引证文献
Kwon J H, Kim J H, Choi S E, et al. Inhibitory effects of phenolic compounds from needles of Pinus densiflora on nitric oxide and PGE2 production [J]. Arch Pharmacal Res, 2010, 33(12): 2011-2016. Wen L R, You L J, Yang X M, et al. Identification of phenolics in Litchi and evaluation of anticancer cell proliferation activity and intracellular antioxidant activity [J]. Free Radic Biol Med, 2015, 84: 171-184. Mahmoud B K, Samy M N, Hamed A N E, et al. Bignanoside A “a new neolignan glucoside” and bignanoside B “a new iridoid glucoside” from Bignonia binata leaves [J]. Phytochem Lett, 2020, 35: 200-205. Zhang Y, Wang J S, Gu Y C, et al. Diverse prieurianin-type limonoid derivatives from the fruits of Aphanamixis grandifolia and their absolute configuration determination [J]. Tetrahedron, 2014, 70(37): 6594-6606. Zhang Y, Wang J S, Luo J, et al. Novel nortriterpenoids from Aphanamixis grandifolia [J]. Chem Pharm Bull, 2011, 59(2): 282-286. Wang X B, Zhang Y, Wang J S, et al. Novel ring A rearranged isomers with γ-lactone from the fruits of Aphanamixis grandifolia [J]. Tetrahedron Lett, 2013, 54(45): 6023-6028. Chen Y W, Wu S L, Dong F W, et al. Four new tirucallane-type triterpenoids from Aphanamixis polystachya [J]. J Asian Nat Prod Res, 2024, 26(8): 883-891. Zeng Q, Guan B, Qin J J, et al. 2,3-Seco- and 3,4-seco-tirucallane triterpenoid derivatives from the stems of Aphanamixis grandifolia Blume [J]. Phytochemistry, 2012, 80: 148-155. Zeng Q, Guan B, Ren J, et al. Aphanamgrandiol A, a new triterpenoid with a unique carbon skeleton from Aphanamixis grandifolia [J]. Fitoterapia, 2013, 86: 217-221. Wang X Y, Tang G H, Yuan C M, et al. Two new tirucallane triterpenoids from Aphanamixis grandifolia [J]. Nat Prod Bioprospect, 2012, 2(5): 222-226. Yang X, Wu S L, Li B J, et al. Triterpenoids from the fruits of Aphanamixis polystachya and their inhibitory activities on nitric oxide production [J]. Fitoterapia, 2023, 171: 105709. Wang D T, Xue Y Y, Zhang Y F, et al. Lignans and phenylpropanoids from the liquid juice of Phyllostachys edulis [J]. Nat Prod Res, 2021, 35(19): 3241-3247. Liao S G, Yuan T, Zhang C, et al. Cinnacassides A–E, five geranylphenylacetate glycosides from Cinnamomum Cassia [J]. Tetrahedron, 2009, 65(4): 883-887. Dagne E, Bisrat D, Van Wyk B E, et al. 10-Hydroxyaloin B 6'-O-acetate, an oxanthrone from Aloe claviflora [J]. J Nat Prod, 1998, 61(2): 256-257. Forster P G, Ghisalberti E L, Jefferies P R. Labdane diterpenes from an Acacia species [J]. Phytochemistry, 1985, 24(12): 2991-2993. Koukoulitsa C, Zervou M, Demetzos C, et al. Comparative docking studies of labdane-type diterpenes with forskolin at the active site of adenylyl cyclase [J]. Bioorg Med Chem, 2008, 16(17): 8237-8243. Zdero C, Bohlmann F, Niemeyer H M. Seco-labdanes and other constituents from Ophryosporus floribundus [J]. Phytochemistry, 1990, 29(10): 3247-3253. Koukoulitsa C, Zervou M, Demetzos C, et al. Comparative docking studies of labdane-type diterpenes with forskolin at the active site of adenylyl cyclase [J]. Bioorg Med Chem, 2008, 16(17): 8237-8243. 秦天丽, 陈彦伍, 吴石丽, 等. 山楝枝叶中两个新的倍半萜[J]. 天然产物研究与开发, 2021, 33(2): 222-226. 张勇, 石倪霏, 谢珍, 等. 黄牛木枝叶中化学成分及其抑制滑膜成纤维细胞增殖活性研究[J]. 中国中药杂志, 2023, 48(18): 5014-5023. Lago J H G, Brochini C B, Roque N F. Terpenes from leaves of Guarea macrophylla (Meliaceae) [J]. Phytochemistry, 2000, 55(7): 727-731. Jiang W, Xiong J, Zang Y, et al. Phytochemical and biological studies on rare and endangered plants endemic to China. Part XIV. Structurally diverse terpenoids from the twigs and needles of the endangered plant Picea brachytyla [J]. Phytochemistry, 2020, 169: 112161. 陈彦伍, 秦天丽, 吴石丽, 等. 华山楝枝叶的化学成分及抗菌活性研究[J]. 中草药, 2020, 51(18): 4614-4619. Taber D F, Bhamidipati R S, Yet L. Phenyldimethylsilyl as an alcohol surrogate in intramolecular Diels-Alder cycloaddition: Synthesis of alpha-dictyopterol [J]. J Org Chem, 1995, 60(17): 5537-5539. Waβmuth-Wagner I, Kalinowski H O, Jork H. Isolation and identification of 11-selinen-4α, 7β-ol and 10-aromadendranol in the essential oil of Murraya koenigii [J]. Planta Med, 1995, 61(2): 196-197. Stakanovs G, Blazevica A, Belyakov S, et al. Semisynthesis of linariophyllenes A–C and rumphellolide H, structure revisions and proposed biosynthesis pathways [J]. J Nat Prod, 2023, 86(10): 2368-2378. Izdihar G, Naini A A, Harneti D, et al. Sesquiterpenoids from the stem bark of Aglaia simplicifolia and their cytotoxic activity against B16-F10 melanoma skin cancer cell [J]. Indones J Chem, 2021, 21(6): 1560. 贾自立, 田文静, 杨任靖, 等. 仙鹤草中木脂素类成分的研究[J]. 中国中药杂志, 2022, 47(11): 2982-2988. 黎灵. 细叶勾儿茶的化学成分研究[D]. 遵义: 遵义医科大学, 2025. Jutiviboonsuk A, Zhang H J, Tan G T, et al. Bioactive constituents from roots of Bursera tonkinensis [J]. Phytochemistry, 2005, 66(23): 2745-2751. 丁雯倩, 史国茹, 庾石山. 龙牙花根中化学成分的研究[J]. 中国中药杂志, 2019, 44(14): 3064-3069. Lu Q R, Wang Y, Tang Z Y, et al. Chemical constituents of Wikstroemia alternifolia and their neuroprotective activities [J]. Nat Prod Res, 2024, 38(6): 986-993. 麦德尚, 陈采欣, 曹嘉敏, 等. 佛手的化学成分研究[J]. 中草药, 2025, 56(2): 421-429. Aung H T, Nikai T, Niwa M, et al. Rosmarinic acid in Argusia argentea inhibits snake venom-induced hemorrhage [J]. J Nat Med, 2010, 64(4): 482-486.
2026年第57卷第15期
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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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