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Two New Alkaloids from Fusarium tricinctum SYPF 7082,an Endophyte from the Root of Panax notoginseng 被引量:5
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作者 Wen-Jie Sun Hong-Tao Zhu +5 位作者 Tian-Yuan Zhang Meng-Yue Zhang Dong Wang Chong-Ren Yang Yi-Xuan Zhang Ying-Jun Zhang 《Natural Products and Bioprospecting》 CAS 2018年第5期391-396,共6页
Panax notoginseng(Araliaceae)is a famous traditional Chinese medicine mainly cultivated in Yunnan and Guangxi provinces of China.Two new alkaloids,rigidiusculamide E(1)and[-(a-oxyisohexanoyl-N-methyl-leucyl)2-](2),tog... Panax notoginseng(Araliaceae)is a famous traditional Chinese medicine mainly cultivated in Yunnan and Guangxi provinces of China.Two new alkaloids,rigidiusculamide E(1)and[-(a-oxyisohexanoyl-N-methyl-leucyl)2-](2),together with two known ones,(-)-oxysporidinone(3)and(-)-4,60-anhydrooxysporidinone(4)were isolated from the mycelia culture of Fusarium tricinctum SYPF 7082,an endophytic fungus obtained from the healthy root of P.notoginseng.Their structures were determined on the basis of extensive spectroscopic analyses.Compounds 1-4 were tested for their inhibitory effects against NO production on Murine macrophage cell line,and the new compound 2 showed significant inhibitory activity on NO production with the IC_(50)value of 18.10±0.16μM. 展开更多
关键词 Fusarium tricinctum SYPF 7082 Endophytic fungus ALKALOIDS Panax notoginseng inhibition on no production
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Anti‑inflammatory and Cytotoxic Triterpenes from the Rot Roots of Panax notoginseng 被引量:2
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作者 Jia‑Huan Shang Guo‑Wei Xu +3 位作者 Hong‑Tao Zhu Dong Wang Chong‑Ren Yang Ying‑Jun Zhang 《Natural Products and Bioprospecting》 CAS 2019年第4期287-295,共9页
Four new protopanaxatriol-type triterpenes(1-2)and glucosides(3-4),were isolated from the rot roots of Panax notoginseng(Burk.)Chen,along with four known ones(5-8).Their structures were elucidated on the basis of exte... Four new protopanaxatriol-type triterpenes(1-2)and glucosides(3-4),were isolated from the rot roots of Panax notoginseng(Burk.)Chen,along with four known ones(5-8).Their structures were elucidated on the basis of extensive spectroscopic analysis(HRESIMS,NMR,UV,IR,and OR)and acidic hydrolysis.The possible transformation pathway of these compounds were also speculated from ginsenoside Rg_(1).Compound 1,with a uniqueα,β-unsaturated ketene in its side chain,showed significant inhibitory effects against NO production on Murine macrophage cells(IC_(50)=4.12±0.20μM)and comparable cytotoxicities against five human cancer cell lines(myeloid leukemia HL-60,lung cancer A-549 cells,hepatocellular carcinoma SMMC7721,breast cancer MCF-7,and colon cancer SW480)to positive control,cisplatin(DDP). 展开更多
关键词 Panax notoginseng Rot root Triterpenes and saponins inhibition on no production CYTOTOXICITY
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Polyhydroxylated eudesmane sesquiterpenoids and sesquiterpenoid glucoside from the flower buds of Tussilago farfara
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作者 LI Yu-Peng YANG Kang +2 位作者 MENG Hui SHEN Tao ZHANG Hua 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2022年第4期301-308,共8页
Chemical fractionation of the n-BuOH partition,which was generated from the EtOH extract of the flower buds of Tussilago farfara,afforded a series of polar constituents including four new sesquiterpenoids(1-4),one new... Chemical fractionation of the n-BuOH partition,which was generated from the EtOH extract of the flower buds of Tussilago farfara,afforded a series of polar constituents including four new sesquiterpenoids(1-4),one new sesquiterpenoid glucoside(5)and one known analogue(6)of the eudesmane type,as well as five known quinic acid derivatives(7-11).Structures of the new compounds were unambiguously characterized by detailed spectroscopic analyses,with their absolute configurations being established by A-ray crystallography,electronic circular dichroism(ECD)calculation and induced ECD experiments.The inhibitory effect of all the isolates against LPS-induced NO production in murine RAW264.7 macrophages was evaluated,with isochlorogenic acid A(7)showing significant inhibitory activity. 展开更多
关键词 Tussilago farfara Eudesmane sesquiterpenoid ANTI-INFLAMMATION no production inhibition Quinic acid derivative
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