Relevant bibliographies by topics / Furoquinoline Alkaloid

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Furoquinoline Alkaloid'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Furoquinoline Alkaloid"

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Halstead, Clynton W., Paul I. Forster, and Peter G. Waterman. "Novel Metabolites from the Stem Bark of Brombya sp. Nova (Gap Creek) (Rutaceae)." Natural Product Communications 1, no. 5 (2006): 1934578X0600100. http://dx.doi.org/10.1177/1934578x0600100502.

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Two piperonyl derivatives, seven coumarins and two furoquinoline alkaloids were isolated from the aerial parts of a new species of Brombya [Brombya sp. nov. (Gap Creek) (Rutaceae)]. Three of the compounds were new natural metabolites; 7-(3,4-methylenedioxyphenyl)octene-2-one (7,8-dehydromoskachen D), the coumarin 6-(1ξ,2ξ,3-trihydroxy-3-methylbutyl)-7-hydroxy-2H-1-benzopyran-2-one, and the furoquinoline alkaloid 4,5,6,7-tetramethoxyfuro[2,3-b]quinoline (5,6,7-trimethoxydictamnine). The secondary metabolites isolated in this study are typical of the Rutaceae, contrasting with earlier studies on
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Magadula, Joseph J., Modest C. Kapingu, Zakaria H. Mbwambo, and Dulcie A. Mulholland. "Secondary Metabolites from Teclea amanuensis (Rutaceae) from Tanzania." Natural Product Communications 3, no. 10 (2008): 1934578X0800301. http://dx.doi.org/10.1177/1934578x0800301020.

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The dichloromethane extract of the stem bark of Teclea amaniensis has yielded two novel furoquinoline alkaloids, 5-[3-methylbut-2-enyl]-4,6,7-trimethoxyfuro[2,3- b]quinoline and 6-(2′,3′-epoxy-3-methylbutyl)-5-hydroxyl-4,7-dimethoxyfuro[2,3- b]quinoline, in addition to an acridone alkaloid, 2-hydroxy-1,3-dimethoxy-10-methylacridone. Three known alkaloids, dictamnine, kokusaginine and evoxanthine, and two known triterpenoids, lupeol and lupeol acetate were also isolated. Structures of the new compounds were established by means of NMR spectroscopic and MS data.
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Szewczyk, Agnieszka, Monika Trepa, and Dominika Zych. "Optimization of the Production of Secondary Metabolites from Furanocoumarin and Furoquinoline Alkaloid Groups in In Vitro Ruta corsica Cultures Grown in Temporary Immersion Bioreactors." Molecules 29, no. 22 (2024): 5261. http://dx.doi.org/10.3390/molecules29225261.

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Ruta corsica is a rare and endemic plant native to Corsica. Due to its limited distribution and the priority to preserve natural sites, has been insufficiently studied. In vitro cultures provide an opportunity to research R. corsica under controlled conditions. In the present study, in vitro cultures of R. corsica were conducted in PlantformTM bioreactors. The study aimed to assess the effects of growth cycle length (5 and 6 weeks) and different concentrations of plant growth regulators (NAA and BAP) at 0.1/0.1, 0.1/0.5, 0.5/0.5, 0.5/1.0, and 1.0/1.0 mg/L on biomass growth and secondary metabo
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de Souza, Rejane C., João B. Fernandes, Paulo C. Vieira, et al. "A New Imidazole Alkaloid and Other Constituents from Pilocarpus grandiflorus and their Antifungal Activity." Zeitschrift für Naturforschung B 60, no. 7 (2005): 787–91. http://dx.doi.org/10.1515/znb-2005-0715.

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The stems of Pilocarpus grandiflorus have afforded the new imidazole alkaloid 4,6-dehydro- 1,2,4,5-tetrahydro-2,5-dioxopilocarpine in addition to the 17 known compounds germanicol, β - amiryn, ocotillone, stigmast-4-en-3-one, 3β -hydroxy-stigmast-5-en-7-one, 6β -hydroxy-stigmast-4- en-3-one, β -sitosterol, scopoletin, 3-(1’,1’-dimethylallyl)-scopoletin, elisin, dictamine, 4-methoxy-2- quinolone, platydesmine, syringaresinol, syringaldehyde, syringic acid and vanillic acid. Their structures were elucidated on the basis of chemical and spectroscopic evidence. The phenolic compounds vanillic acid
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Mohammed, Magdy M. D., and Eman R. El-Sharkawy. "Cytotoxic new furoquinoline alkaloid isolated from Ammi majus L. growing in Egypt." Natural Product Research 31, no. 6 (2016): 645–52. http://dx.doi.org/10.1080/14786419.2016.1217858.

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Yang, Zhong-duo, Dong-bo Zhang, Jin Ren, and Ming-jun Yang. "Skimmianine, a furoquinoline alkaloid from Zanthoxylum nitidum as a potential acetylcholinesterase inhibitor." Medicinal Chemistry Research 21, no. 6 (2011): 722–25. http://dx.doi.org/10.1007/s00044-011-9581-9.

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El-Sawy, Eslam R., Ahmed B. Abdelwahab, and Gilbert Kirsch. "Maculine: a furoquinoline alkaloid from the family Rutaceae: sources, syntheses and biological activities." Arkivoc 2020, no. 7 (2020): 82–93. http://dx.doi.org/10.24820/ark.5550190.p011.200.

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Chang, Gwo-Jyh, Mei-Hwan Wu, Wen-Pin Chen, Sheng-Chu Kuo, and Ming-Jai Su. "Electrophysiological characteristics of antiarrhythmic potential of acrophyllidine, a furoquinoline alkaloid isolated fromAcronychia halophylla." Drug Development Research 50, no. 2 (2000): 170–85. http://dx.doi.org/10.1002/1098-2299(200006)50:2<170::aid-ddr7>3.0.co;2-w.

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Gokmen, Aysegul A., Hüseyin Can, Hüsniye Kayalar, Bayram Pektaş, and Selçuk Kaya. "In vitro anti-Trichomonas vaginalis activity of Haplophyllum myrtifolium." Journal of Infection in Developing Countries 13, no. 03 (2019): 240–44. http://dx.doi.org/10.3855/jidc.10854.

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Introduction: In the classic treatment of Trichomonas vaginalis infection, although metronidazole has been used since the 1960s, there has been an increase in MTZ-resistant T. vaginalis strains and failure in the treatment of trichomoniasis causes serious concerns. Therefore, the present study aimed to investigate the in vitro antitrichomonal activities of extracts (ethanol and total alkaloid) and pure compounds (chrysosplenetin, dictamnine, gamma-Fagarine, skimmianine) of H. myrtifolium against T. vaginalis.&#x0D; Methodology: H. myrtifolium was collected from the town of Honaz in Denizli, lo
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Kuete, Victor, Hugues Fouotsa, Armelle T. Mbaveng, Benjamin Wiench, Augustin E. Nkengfack, and Thomas Efferth. "Cytotoxicity of a naturally occurring furoquinoline alkaloid and four acridone alkaloids towards multi-factorial drug-resistant cancer cells." Phytomedicine 22, no. 10 (2015): 946–51. http://dx.doi.org/10.1016/j.phymed.2015.07.002.

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Dissertations / Theses on the topic "Furoquinoline Alkaloid"

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Zanon, Graciane. "Análise Fitoquímica e Estudo das Atividades Antimicrobiana, Antioxidante e de Inibição da Enzima Acetilcolinesterase das espécies Zanthoxylum rhoifolium e Zanthoxylum hyemale." Universidade Federal de Santa Maria, 2010. http://repositorio.ufsm.br/handle/1/10472.

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The present study was designed to evaluate the biological activity from the stem bark of Zanthoxylum rhoifolium and Zanthoxylum hyemale. The neutral methanol extract and fractions of this extract, the basic fractions that were obtained after acid-basic extraction from the methanolic extract, and pure compounds isolated from these fraction, were investigated in vitro for antimicrobial activity, antioxidant potential and for acetylcholinesterase inhibition. From the dichlorometane fraction of Zanthoxylum rhoifolium were isolated three furoquinoline alkaloids: skimianine, 8-hidroxy-4,7-dimetoxy-f
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Manasfi, Youssef. "Lutte contre les pathogènes telluriques en contexte horticole : cas du pathosystème Choisya ternata/ Phytophthora spp." Thesis, Normandie, 2017. http://www.theses.fr/2017NORMR082.

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Choisya ternata est une plante ornementale souvent touchée par la maladie de la pourriture racinaire provoquée par Phytophthora. Cette maladie peut induire de pertes allant jusqu’à 80 %, ce qui implique l’utilisation intensive de produits phytosanitaires. Afin de limiter l’utilisation de ces produits toxiques, une meilleure connaissance des acteurs de la défense des plantes est nécessaire. Pour cela, les objectifs de cette thèse sont I) d’identifier les espèces du genre Phytophthora pathogènes de C. ternata, II) d’étudier des acteurs de défense au niveau racinaire et III) de développer une app
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林宗平. "Investigation of isolation and synthesis of natural furoquinolone alkaloids constituents in Rutaceae." Thesis, 1987. http://ndltd.ncl.edu.tw/handle/36721438684695442162.

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Book chapters on the topic "Furoquinoline Alkaloid"

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Ikuta, Akira. "Indolopyridoquinazoline, Furoquinoline, Canthinone and Protoberberine-Type Alkaloids from Phellodendron amurense Callus Tissues." In Medicinal and Aromatic Plants XII. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-08616-2_11.

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Couillerot, E., C. Caron, C. Trentesaux, J. C. Chenieux, and J. C. Audran. "Fagara zanthoxyloides Lam. (Rutaceae): In Vitro Culture and the Production of Benzophenanthridine and Furoquinoline Alkaloids." In Medicinal and Aromatic Plants XI. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-662-08614-8_8.

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Omujal, Francis. "Phytochemistry and Ethnopharmacology of Vebris nobilis Delile (Rutaceae)." In Pharmacognosy - Medicinal Plants [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96809.

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Vepris nobilis Mziray (formerly Teclea noblis Delile) is an ever-green plant in the tropical climate. The different parts (leaves, stem bark, roots and fruits) of this plant are popular for treatment of various diseases including; malaria, rheumatism, arthritis, pneumonia, cough, fever, measles, asthma, common cold, headache, join and chest pains and as antithelmintic. Several phytochemical compounds including quinoline and furoquinoline alkaloids, terpenoids and flavonoids have been isolated from the different plant. Pharmacological investigations on the different crude extracts and isolated
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Journal articles
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