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1.
Two new indole alkaloids, cadambinic acid ( 1 ) and isonauclefidine ( 2 ), were isolated from the bark of Anthocephalus chinensis. The structures were identified by spectroscopic methods, and the compounds were tested for their biological activities. Both compounds showed weak cytotoxicities against A549, BGC‐823, and HeLa cells in biological assays. 相似文献
2.
Hua Zhou Hong‐Ping He Ning‐Chuan Kong Yue‐Hu Wang Xiang‐Dong Liu Xiao‐Jiang Hao 《Helvetica chimica acta》2006,89(3):515-519
Three new indole alkaloids, 11,12‐de(methylenedioxy)danuphylline ( 1 ), methyl (2β,11β,12β,19α)‐6,7‐didehydro‐8,21‐dioxo‐11,21‐cycloaspidospermidine‐2‐carboxylate ( 2 ), and (2β,5β)‐aspidofractinin‐16‐ol ( 3 ) were isolated from Kopsia officinalis, together with 16 known compounds. Their structures were determined by spectroscopic methods. The isolated known compound (?)‐12‐methoxykopsinaline displayed antimanic effects in Drosophila, with an IC50 value of 12.5 μg/ml. 相似文献
3.
Xing‐De Wu Lei Wang Juan He Xing‐Yao Li Liao‐Bin Dong Xun Gong Xiu Gao Liu‐Dong Song Yan Li Li‐Yan Peng Qin‐Shi Zhao 《Helvetica chimica acta》2013,96(12):2207-2213
Two new indole alkaloids, 5‐oxodolichantoside ( 1 ) and deglycocadambine ( 2 ), were isolated from the twigs and leaves of Emmenopterys henryi, together with four known indole alkaloids and five known iridoids. The structures of the new compounds were elucidated on the basis of extensive spectroscopic analyses, including 1D‐ and 2D‐NMR experiments, and confirmed by single‐crystal X‐ray diffraction studies. This is the first report on the isolation of indole alkaloids from this species. The indole alkaloids were evaluated for their cytotoxic activities against five human cancer lines. 相似文献
4.
Shuang Liang Hai‐Sheng Chen Yun‐Heng Shen Li Jin Wei‐Dong Zhang 《Helvetica chimica acta》2007,90(8):1467-1470
Flabelliformides A ( 1 ) and B ( 2 ), containing a novel C20 indole core, have been isolated from the stems of Ervatamia flabelliformis. The structures of 1 and 2 were elucidated on the basis of spectral analysis and X‐ray crystallography. 相似文献
5.
Xu‐Jia Hu Hong‐Ping He Hua Zhou Ying‐Tong Di Xian‐Wen Yang Xiao‐Jiang Hao Ling‐Yi Kong 《Helvetica chimica acta》2006,89(7):1344-1350
Three new indole alkaloids, 10‐methoxy‐16‐de(methoxycarbonyl)pagicerine ( 1 ), (5β)‐17‐O‐deacetyl‐5,11‐dimethoxyakuammiline ( 2 ), and ((16S,19E)‐N1‐(hydroxymethyl)isositsirikine ( 3 ) were isolated from the roots of Rauvolfia yunnanensis, together with seven known alkaloids. The structures of the new compounds were elucidated by in‐depth spectroscopic and mass‐spectrometric analyses. 相似文献
6.
Jucimar J. de Souza Leda Mathias Raimundo Braz‐Filho Ivo J. Curcino Vieira 《Helvetica chimica acta》2010,93(3):422-429
Two new monoterpene indole alkaloids named ibogamine‐7,8‐dione ( 1 ) and 12‐methoxyvoachalotine ( 2 ), and eight known ones, coronaridine ( 3 ), coronaridine hydroxyindolenine ( 4 ), 5‐oxocoronaridine ( 5 ), 3‐oxocoronaridine hydroxyindolenine ( 6 ), 3‐oxocoronaridine ( 7 ), vobasine ( 8 ), ibogamine ( 9 ), and olivacine ( 10 ), were isolated from a CH2Cl2 extract of the root bark from Tabernaemontana hystrix. The structures of the compounds were elucidated on the basis of spectroscopic data analyses, mainly 1H‐ and 13C‐NMR, including 2D experiments (1H,1H‐COSY, HMBC, and HMQC). 相似文献
7.
Gaétan Bayiha Ba Njock Trixie Ann Bartholomeusz Dominique Ngono Bikobo Mohammadali Foroozandeh Rupali Shivapurkar Philippe Christen Dieudonné Emmanuel Pegnyemb Damien Jeannerat 《Helvetica chimica acta》2013,96(7):1298-1304
A new indole alkaloid, calanthumindole ( 4 ), and three known biflavonoids, amentoflavone, sequoiaflavone, and podoscarpusflavone B, were isolated from Campylospermum calanthum (Ochnaceae). Calanthumindole is a new indole alkaloid of the serotobenine family characterized by the presence of a C?C bond between atoms C(7′) and C(8′) of the furan ring. This is the first compound to have a fully unsaturated furan ring among the members of this family. The combination of NMR and DFT allowed the determination and comparison of the 3D structures and relevant conformational characteristics of serotobenine ( 1 ), flavumindole ( 2 ), and calanthumindole ( 4 ). 相似文献
8.
Heloisa A. Guimarães Ivo J. C. Vieira Raimundo Braz‐Filho Antônio E. M. Crotti Vitor S. dos Almeida Renata C. de Paula 《Helvetica chimica acta》2013,96(9):1793-1800
Two novel indole alkaloids with plumeran skeleton, N‐benzoyl‐12‐demethoxycylindrocarine and N‐cinnamoyl‐12‐demethoxycylindrocarine ( 1 and 2 , resp.), were isolated from the MeOH extract of the stem bark of Aspidosperma cylindrocarpon Müll .Arg . These compounds were obtained by high‐speed counter‐current chromatography, and their structures were elucidated on the basis of their NMR (1D and 2D) data. They were tested in vitro against chloroquine‐resistant strains of Plasmodium falciparum, and only 2 showed a weak activity (IC50 127.97 ng/ml with respect to the standard drug). Several other known compounds, comprising steroids, flavonoids, the rarely found atraric acid, as well as the previously reported alkaloid 3 , were also isolated by conventional chromatographic techniques. 相似文献
9.
Javid Hussain Hidayatullah Khan Liaqat Ali Abdul Latif Khan Najeeb Ur Rehman Sajid Jahangir Ahmed Al‐Harrasi 《Helvetica chimica acta》2015,98(5):719-723
The phytochemical investigations on Cleome droserifolia resulted in the isolation and characterization of a new indole alkaloid, 5‐hydroxy‐2‐methoxy‐1‐methyl‐1H‐indole‐3‐carbaldehyde ( 1 ). The structure elucidation was carried out on the basis of 1D‐ and 2D‐NMR techniques. In addition to 1 , two known aromatic derivatives, veratrol ( 2 ) and 2‐methoxy‐4‐methylacetophenone ( 3 ), were also obtained. All these compounds were purified by repeated column chromatography of the CH2Cl2 fraction obtained from MeOH extract of Cleome droserifolia. The structure of the new compound 1 was finally confirmed by the combined 1D (1H‐ and 13C‐) and 2D (H? C correlations; HMBC and HSQC) NMR and IR spectroscopy, mass spectrometry (MS), and UV absorption spectroscopy techniques. The comparison of the physical and spectroscopic data with those in the literature provided evidence for the structure confirmation of known compounds. All the purified compounds were subjected to urease and α‐glucosidase enzymes inhibition. The results showed that compound 1 was more potent with an IC50 value 11.97±2.067 μg/ml towards urease inhibition, while the activity of α‐glucosidase enzyme was marginal. 相似文献
10.
Two new 11‐hydroxy‐substituted gelsedine‐type indole alkaloids, named 11,14‐dihydroxygelsenicine ( 1 ) and 11‐hydroxygelsenicine ( 2 ), together with six known alkaloids, i.e., koumine, gelsemine, 14‐hydroxygelsenicine, 11‐hydroxyhumantenine, gelsenicine, and (19Z)‐akuammidine, were isolated from the EtOH extract of the stems of Gelsemium elegans Benth. Their structures were determined mainly by means of spectroscopic analyses including HR‐ESI‐MS and 2D‐NMR (HSQC, HMBC, 1H,1H‐COSY). The configuration of 1 was confirmed by X‐ray‐diffraction analysis. 相似文献
11.
Shuang Liang Hai‐Sheng Chen Yun‐Heng Shen Wei‐Dong Zhang Yong‐Sheng Jin Run‐Hui Liu 《Helvetica chimica acta》2008,91(2):239-243
The three new monoterpenoid indole alkaloids 1 – 3 were isolated from the stems of Ervatamia flabelliformis. The structures were elucidated on the basis of spectral analysis and chemical derivatization. 相似文献
12.
Jiang Hu Wei‐Dong Zhang Yun‐Heng Shen Chuan Zhang Run‐Hui Liu Xi‐Ke Xu Bin Wang 《Helvetica chimica acta》2007,90(4):720-722
Two novel alkaloids, 4,5‐dihydroxy‐1‐methyl‐3‐oxo‐2‐(trichloromethyl)‐3H‐indolium chloride ( 1 ) and 4‐(2‐methoxyethyl)‐N,N‐dimethylbenzenamine ( 2 ), were isolated from the EtOH extract of the roots of Zanthoxylum nitidum. Their structures were identified on the basis of spectroscopic and mass‐spectrometric analyses. 相似文献
13.
Sheng‐Xin Cai De‐Hai Li Tian‐Jiao Zhu Feng‐Ping Wang Xiang Xiao Qian‐Qun Gu 《Helvetica chimica acta》2010,93(4):791-795
Two new indole alkaloids, arsindolines A and B ( 1 and 2 , resp.), together with six known indole alkaloids, were isolated from a marine‐derived bacterium strain CB101, identified as Aeromonas sp. Their structures were established by spectroscopic methods, and their antitumor activities were evaluated by SRB and MTT methods. 相似文献
14.
Bing‐Jie Zhang Ju‐Ming Yan Zi‐Kun Wu Ya‐Ping Liu Mei‐Fen Bao Gui‐Guang Cheng Xiao‐Dong Luo Xiang‐Hai Cai Yan Li 《Helvetica chimica acta》2013,96(12):2288-2298
Ten new monoterpenoid indole alkaloids, ochroborines A and B ( 1 and 2 , resp.), 10‐hydroxyisovallesiachotamine ( 3 ), 10‐hydroxyisositsirikine ( 4 ), 10,11‐dimethoxysitsirikine ( 5 ), 10‐methoxyapoyohimbine ( 6 ), 10‐hydroxyakuammidine ( 7 ), akuammidine 17‐O‐β‐D ‐glucoside ( 8 ), 15α‐hydroxyapparicine ( 9 ), and 15α‐hydroxy‐10‐methoxyapparicine ( 10 ), and 24 known alkaloids were isolated from leaves and twigs of Ochrosia borbonica J. F.Gmel . These structures were elucidated based on 1D‐ and 2D‐NMR, FT‐IR, UV, and MS data. 10‐Hydroxyisovallesiachotamine ( 3 ), ellipticine, and 10‐methoxyellipticine showed cytotoxic activities against five human cancer cell lines. 相似文献
15.
Xiang‐Hai Cai Chun‐Xia Zeng Tao Feng Yan Li Xiao‐Dong Luo 《Helvetica chimica acta》2010,93(10):2037-2044
Three new monoterpenoid indole alkaloids, (14α,15α)‐14,15‐epoxyaspidofractinine ( 1 ) and maireines A and B ( 2 and 3 , resp.), together with 19 known alkaloids, were isolated from the leaves and twigs of Alstonia mairei. The structures of the new compounds were elucidated by 1D‐ and 2D‐NMR spectroscopic methods in combination with MS experiments. 相似文献
16.
Five new indole alkaloids, viz., kopsiloscine G ( 2 ), kopsidarine ( 4 ), kopsimaline F ( 6 ), kopsidine C N‐oxide ( 7 ), and aspidophylline B ( 9 ), in addition to 17 other known alkaloids, were obtained from the leaf and stem‐bark extract of the Malaysian Kopsia singapurensis. The structures were determined by using NMR and MS analysis. The results are compared with the alkaloidal composition of another sample of K. singapurensis, collected from the same location but at a different time of the year, as well as with other samples of K. singapurensis collected from different locations. 相似文献
17.
From the methanolic extract of the roots of Acacia confusa Merr. (Leguminosae), (‐)‐2,3‐cis‐3,4‐cis‐4′‐methoxy‐3,3′,4,7,8‐pentahydroxyflavan ( 1 ), (‐)‐2,3‐cis‐3,4‐cis‐3,3′,4,4′,7,8‐hexahydroxyflavan ( 2 ), (‐)‐2,3‐trans‐3′,4′,7,8‐tetrahydroxydihydroflavonol ( 3 ), (+)‐catechin ( 4 ), (‐)‐epicatechin ( 5 ), 3′,4′,7,8‐tetrahydroxyflavonol ( 6 ) together with N‐methyltryptamine ( 7 ) and N,N‐dimethyltryptamine ( 8 ) were isolated, and their structures were established by analysis of their spectroscopic data. Among them, compound 1 was a new flavonoid. Additionally, the results of chromatographic bioassay on lettuce seeds indicated that compounds 7 and 8 exhibited significant phytotoxicity at a concentration lower than 14 mM. 相似文献
18.
Cheng‐Jian Tan Yu Zhang Ning‐Chuan Kong Ying‐Tong Di Xiao‐Jiang Hao 《Helvetica chimica acta》2015,98(1):72-77
Four new indole alkaloids, trigonoliimines D–G ( 1 – 4 , resp.), were isolated from Trigonostemon lii. Their structures were elucidated by spectroscopic methods, including extensive 1D‐ and 2D‐NMR experiments. 相似文献
19.
Kuan‐Hon Lim Yun‐Yee Low Guan‐Huat Tan Toh‐Seok Kam Tuck‐Meng Lim 《Helvetica chimica acta》2008,91(8):1559-1566
Two new indole alkaloids, 12‐methoxykopsine ( 6 ) and danuphylline B ( 7 ), were obtained from the leaf extract of the Malayan Kopsia species, K. arborea, and their structures established by spectroscopic analysis. An electrochemically‐mediated partial synthesis of the ring‐opened alkaloid, danuphylline B from the hexacyclic alkaloid, methyl N(1)‐de(methoxycarbonyl)chanofruticosinate was carried out. 相似文献
20.
Xin Gen Luo Hai Sheng Chen Shuang Liang Mao Huang Wei Dong Xuan Li Jin College of Pharmacy Second Military Medical University Shanghai China Department of Pharmacy Guangzhou Military General Hospital Guangzhou China Center of New Drug Evaluation Institute of Basic Medical Sciences Second Military Medical University Shanghai China 《中国化学快报》2007,18(6):697-699
Six indole alkaloids were isolated from the stems of Ervatamia yunnanensis. Among them, yunnanensine (I) is new. The other five are known alkaloids, namely: 19,20-E-vallesamine (II), 19s-heyneanine (HI), ibogaine (IV), ibogamine (V), coronaridine (VI). The structural elucidation of the alkaloids was based on spectral means. 相似文献