Relevant bibliographies by topics / Furoquinolines

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

Academic literature on the topic 'Furoquinolines'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Furoquinolines"

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Fayol, Aude, and Jieping Zhu. "Synthesis of Furoquinolines by a Multicomponent Domino Process." Angewandte Chemie International Edition 41, no. 19 (2002): 3633–35. http://dx.doi.org/10.1002/1521-3773(20021004)41:19<3633::aid-anie3633>3.0.co;2-t.

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Paira, Rupankar, Tarique Anwar, Maitreyee Banerjee, et al. "Copper–phenanthroline catalysts for regioselective synthesis of pyrrolo[3′,4′:3,4]pyrrolo[1,2-a]furoquinolines/phenanthrolines and of pyrrolo[1,2-a]phenanthrolines under mild conditions." Beilstein Journal of Organic Chemistry 10 (March 20, 2014): 692–700. http://dx.doi.org/10.3762/bjoc.10.62.

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A new series of pyrrolo[3′,4′:3,4]pyrrolo[1,2-a]furoquinolines/phenanthrolines and pyrrolo[1,2-a]phenanthrolines were efficiently built up from an 8-hydroxyquinoline derivative or phenanthroline via 1,3-dipolar cycloaddition reaction involving non-stabilized azomethine ylides, generated in situ from the parent furo[3,2-h]quinoliniums/phenanthroliums, in presence of a copper(II) chloride–phenanthroline catalytic system. The methodology combines general applicability with high yields.
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Chen, Keh-Shaw, Ya-Ling Chang, Che-Ming Teng, Chieh-Fu Chen, and Yang-Chang Wu. "Furoquinolines with Antiplatelet Aggregation Activity from Leaves ofMelicope confusa." Planta Medica 66, no. 01 (2009): 80–81. http://dx.doi.org/10.1055/s-0029-1243116.

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Ferreira, Maria Elena, Antonieta Rojas de Arias, Gloria Yaluff, et al. "Antileishmanial activity of furoquinolines and coumarins from Helietta apiculata." Phytomedicine 17, no. 5 (2010): 375–78. http://dx.doi.org/10.1016/j.phymed.2009.09.009.

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Savina, S. A., V. M. Lyubchanskaya, L. M. Alekseeva, A. S. Shashkov, and V. G. Granik. "Synthesis of novel furoquinolines and furobenzodiazepines from tetronic acid." Russian Chemical Bulletin 56, no. 11 (2007): 2298–304. http://dx.doi.org/10.1007/s11172-007-0363-y.

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Chosson, Elizabeth, Anne-Emmanuelle Hay, Angele Chiaroni, et al. "Sarcodifurines A and B, Two New Furoquinolines from Sarcomelicope follicularis." HETEROCYCLES 63, no. 9 (2004): 2043. http://dx.doi.org/10.3987/com-04-10146.

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Kumar, Devadoss Karthik, Rayappan Rajkumar, and Subramaniam Parameswaran Rajendran. "Robust synthesis of linear and angular furoquinolines using Rap–Stoermer reaction." Chemistry of Heterocyclic Compounds 52, no. 5 (2016): 322–25. http://dx.doi.org/10.1007/s10593-016-1885-8.

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Mahesh, M., Ch Venkateshwar Reddy, K. Srinivasa Reddy, P. V. K. Raju, and V. V. Narayana Reddy. "Imino Diels–Alder Reactions: Efficient Synthesis of Pyrano and Furoquinolines Catalyzed by ZrCl4." Synthetic Communications 34, no. 22 (2004): 4089–104. http://dx.doi.org/10.1081/scc-200036586.

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Cheng, Juei-Tang, Tzen Kwan Chang, and Ih-Sheng Chent. "Skimmianine and related furoquinolines function as antagonists of 5-hydroxytryptamine receptors in animals." Journal of Autonomic Pharmacology 14, no. 5 (1994): 365–74. http://dx.doi.org/10.1111/j.1474-8673.1994.tb00617.x.

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Paulini, Hubert, Reiner Waibel, and Oskar Schimmer. "Mutagenicity and structure-mutagenicity relationships of furoquinolines, naturally occurring alkaloids of the Rutaceae." Mutation Research Letters 227, no. 3 (1989): 179–86. http://dx.doi.org/10.1016/0165-7992(89)90043-2.

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Dissertations / Theses on the topic "Furoquinolines"

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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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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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Sackett, Tara Elizabeth. "Furoquinolines of the Rutaceae and their role in plant-lepidopteran interactions." Thesis, 2000. http://hdl.handle.net/2429/10752.

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Two furoquinoline alkaloids, skimmianine and dictamnine, were purified from the dried leaves of Skimmia japonica (Rutaceae) and dried root of Dictamnus albus (Rutaceae), respectively. The furoquinolines were isolated through acid fractionation and silica gel column chromatography, and their identity was confirmed through HPLC and mass spectroscopic analysis. Skimmianine and dictamnine, as well as the furanocoumarins 8-methoxypsoralen (8-MOP) and 5-methoxypsoralen (5-MOP) were quantified in leaf tissue of S. japonica and Ruta graveolens (Rutaceae). Of these compounds, S. japonica contain
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Chen, I.-Li, and 陳意莉. "Studies on the Synthesis and Biological Activities of Furoquinoline Derivatives." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/b7965t.

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博士<br>高雄醫學大學<br>藥學研究所<br>91<br>Some 4-anilinofuro[2,3-b]quinoline derivatives were synthesized from dictamnine, a natural alkaloid, and evaluated for their cytotoxicity in the NCI’s full panel of 60 human cancer cell lines derived from nine cancer cell types, including leukemia, non-small-cell lung cancer, colon cancer, CNS cancer, melanoma, ovarian cancer, renal cancer, prostate cancer, and breast cancer. 1-[4-(Furo[2,3-b]quinolin-4-ylamino)phenyl]ethanone (5) (GI50 = 0.025 mM), bearing an 4-acetylanilino substituent at C(4) of furo[2,3-b]quinoline, was more active than its 3-acetylanilino co
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Tan, Jui-Ning, and 旦瑞寧. "Mechanical, electrophysiological and antiarrhythmic action of furoquinoline derivative, CJP-C-12 on rat heart." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/59228101499599957858.

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碩士<br>國立臺灣大學<br>藥理學研究所<br>87<br>Abstract CJP-C-12, a new furoquinoline alkaloid derivative, was found to have positive inotropic and negative chronotropic effect in rat cardiac tissues. The electrophysiological effects and antiarrhythmic potential of this compound were examined in the present study. 1. CJP-C-12 increased the twitch tension of driven left atria and right ventricular strips concentration-dependently, but decreased the spontaneous beating rate of rat right atria. 2. Atenolol (3 mM) could partially inhibit the inotropic effect of low conce
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Book chapters on the topic "Furoquinolines"

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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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