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Tangutidines A-C,Three Amphoteric Diterpene Alkaloids from Aconitum tanguticum 被引量:2
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作者 Hao-Yi Li Bing-Chao Yan +2 位作者 Li-Xin Wei Han-Dong Sun Pema-Tenzin Puno 《Natural Products and Bioprospecting》 CAS 2021年第4期459-464,共6页
Three new diterpene alkaloids,tangutidines A-C(1-3),and four known alkaloids(4-7)were isolated from the whole plant of Aconitum tanguticum,from which amphoteric diterpene alkaloids(1-3)were obtained for the first time... Three new diterpene alkaloids,tangutidines A-C(1-3),and four known alkaloids(4-7)were isolated from the whole plant of Aconitum tanguticum,from which amphoteric diterpene alkaloids(1-3)were obtained for the first time.The structures of 1-3 were elucidated by detailed interpretation of spectroscopic data,including MS and NMR data.All of them were evaluated for their cytotoxic activities. 展开更多
关键词 Aconitum tanguticum Amphoteric diterpene alkaloids Tangutidine Cytotoxic activity
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Two new diterpene alkaloids from Delphinium chrysotrichum 被引量:1
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作者 Yang Qing He Xiao Mei Wei +1 位作者 Yi Li Han Li Ming Gao 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第5期545-547,共3页
Chemical investigation on the ethanol extract from the whole plants of Delphinium chrysotrichum resulted in the isolation of two new diterpene alkaloids named delphatisine A (1) and delphatisine B (2), respectivel... Chemical investigation on the ethanol extract from the whole plants of Delphinium chrysotrichum resulted in the isolation of two new diterpene alkaloids named delphatisine A (1) and delphatisine B (2), respectively. The structures of the new compounds were deduced on the basis of their spectral data (IR, HREIMS, EIMS, 1 D, 2D-NMR). This is the first report on the isolation of diterpenoid alkaloids from the D. chrysotrichum. 展开更多
关键词 Delphinium chrysotrichum diterpene alkaloids Delphatisine A Delphatisine B
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Two New Diterpene Alkaloids from the Roots of Spiraea japonica var.Acuta 被引量:1
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作者 Hong Ping HE Yue Mao SHEN +3 位作者 Xiao Sheng YANG Bin Gui WANG Ling LI Xiao Jiang HAO 《Chinese Chemical Letters》 SCIE CAS CSCD 2001年第1期67-68,共2页
Chemical investigation on the ethanol extract from the roots of Spiraea japonica var. acuta resulted in the isolation of two new diterpene alkaloids named spiratines A and B (1-2), respectively.
关键词 Spiraea japonica var.acuta diterpene alkaloids spiratine A spiratine B.
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TWO NEW C_(19)-DITERPENE ALKALOIDS FROM DELPHINIUM SWINANENSE VAR LEPTOPOGON
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作者 Suo Hing ZHANG Qing Yu OU Wei Le YU(Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000) 《Chinese Chemical Letters》 SCIE CAS CSCD 1994年第9期755-756,共2页
An investigation of the alkaloids of Delphinium swinanense var. leptopogon resulted in the isolation and identification of two new C(19)-diterpene alkaloids named swinanine A and B, together with one known tatsiensine... An investigation of the alkaloids of Delphinium swinanense var. leptopogon resulted in the isolation and identification of two new C(19)-diterpene alkaloids named swinanine A and B, together with one known tatsiensine. The structures of the new alkaloids were established from spectraf evidence. 展开更多
关键词 VAR diterpene alkaloidS FROM DELPHINIUM SWINANENSE VAR LEPTOPOGON TWO NEW C
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Two new diterpene alkaloids from the South China Sea Sponge Agelas aff. nemoechinata 被引量:2
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作者 Tao Li Bin Wang +5 位作者 Nicole J.de Voogd Xu-Li Tang Qi Wang Mei-Jun Chu Ping-Lin Li Guo-Qiang Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2016年第7期1048-1051,共4页
Two new N-methyladenine-containing diterpenes,nemoechines F(l)and G(2),were isolated from the South China Sea sponge Agelas aff.nemoechinata.The structures were assigned on the basis of spectroscopic date.Compound... Two new N-methyladenine-containing diterpenes,nemoechines F(l)and G(2),were isolated from the South China Sea sponge Agelas aff.nemoechinata.The structures were assigned on the basis of spectroscopic date.Compound 2 showed weak activity against Jurkat cell lines with IC50 of 17.1 μmol/L 展开更多
关键词 South China Sea Marine sponge Agelas diterpene alkaloids CYTOTOXIC
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Diterpenoid alkaloids from a Tibetan medicinal plant Aconitum richardsonianum var. pseudosessiliflorum and their cytotoxic activity 被引量:4
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作者 Yang-Qing He Bing-Hua Yao Zhan-Ying Ma 《Journal of Pharmaceutical Analysis》 SCIE CAS 2011年第1期57-59,共3页
The chemical constituents from Aconitum richardsonianum var.pseudosessiliflorum were investigated.The roots of this plant were extracted three times with 90% EtOH at the room temperature.The ethanol extracts were comb... The chemical constituents from Aconitum richardsonianum var.pseudosessiliflorum were investigated.The roots of this plant were extracted three times with 90% EtOH at the room temperature.The ethanol extracts were combined and concentrated under reduced pressure to yield residue,which was suspended in water and successively partitioned with chloroform.The chloroform extraction was isolated and purified by silica gel and Sephadex LH-20 column chromatography.Six compounds were isolated and elucidated as delelatine(1),isodelpheline(2),3-acetylaconitine(3),isoatisine(4),nordhagenine A(5)and yunaconitine(6).Compounds 1-5 were obtained from Aconitum Brunneum for the first time.Compound(1)showed significant cytotoxic activities(IC50=4.36 μM)against the human tumor cell line P388. 展开更多
关键词 Aconitum richardsonianum var.pseudosessiliflorum RANUNCULACEAE diterpene alkaloids cytotoxic activity
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Biological Activity and Molecular Mechanism of Bullatine G
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作者 Jian LIU Jinglong CAO +3 位作者 Hui XUE Yannan LI Wenshuang HOU Chenghao JIN 《Medicinal Plant》 CAS 2023年第2期90-92,96,共4页
Bullatine G has many biological effects such as anti-inflammatory,anti-anxiety,anti-tumor,anti-arrhythmia and anti-heart failure effect.In order to provide a theoretical basis for the further study and clinical applic... Bullatine G has many biological effects such as anti-inflammatory,anti-anxiety,anti-tumor,anti-arrhythmia and anti-heart failure effect.In order to provide a theoretical basis for the further study and clinical application of bullatine G,this article reviews the biological activity of bullatine G in recent years. 展开更多
关键词 Bullatine G diterpene alkaloids Anti-inflammatory effect Anticancer effect Pharmacological effects
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