Relevant bibliographies by topics / Acridine(amino-9 chloro-6 methoxy-2)

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Academic literature on the topic 'Acridine(amino-9 chloro-6 methoxy-2)'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Acridine(amino-9 chloro-6 methoxy-2)"

1

Busto, Natalia, Begoña García, José M. Leal, et al. "ACMA (9-amino-6-chloro-2-methoxy acridine) forms three complexes in the presence of DNA." Physical Chemistry Chemical Physics 13, no. 43 (2011): 19534. http://dx.doi.org/10.1039/c1cp22158b.

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Constant, J. F., T. R. O'Connor, J. Lhomme, and J. Laval. "9-[(10-(aden-9-yl)-4,8-diazadecyl)amino]-6-chloro-2-methoxy-acridine incises DNA at apurinic sites." Nucleic Acids Research 16, no. 6 (1988): 2691–703. http://dx.doi.org/10.1093/nar/16.6.2691.

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3

Aly, Enayat I., and Ashraf H. Abadi. "Synthesis and antitubercular activity of 6-chloro (unsubstituted)-2-methoxy-9-substituted acridine derivatives." Archives of Pharmacal Research 27, no. 7 (2004): 713–19. http://dx.doi.org/10.1007/bf02980137.

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4

Lisboa, Thaís, Daiana Silva, Sâmia Duarte, et al. "Toxicity and Antitumor Activity of a Thiophene–Acridine Hybrid." Molecules 25, no. 1 (2019): 64. http://dx.doi.org/10.3390/molecules25010064.

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The antitumor effects of thiophene and acridine compounds have been described; however, the clinical usefulness of these compounds is limited due to the risk of high toxicity and drug resistance. The strategy of molecular hybridization presents the opportunity to develop new drugs which may display better target affinity and less serious side effects. Herein, 2-((6-Chloro-2-methoxy-acridin-9-yl)amino)-5,6,7,8-tetrahydro-4H-cyclohepta[b]-thiophene-3-carbonitrile (ACS03), a hybrid thiophene–acridine compound with antileishmanial activity, was tested for toxicity and antitumor activity. The toxic
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Jayat-Vignoles, Chantal, Marie-H�l�ne Ratinaud, and Raymond Julien. "3-Amino-6-methoxy-9-(2-hydroxyethylamino) acridine: A new fluorescent dye to detect mycoplasma contamination in cell cultures." Cytotechnology 4, no. 2 (1990): 191–94. http://dx.doi.org/10.1007/bf00365100.

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Zhang, Wei, Bin Zhang, Wei Zhang, et al. "Synthesis and antiproliferative activity of 9-benzylamino-6-chloro-2-methoxy-acridine derivatives as potent DNA-binding ligands and topoisomerase II inhibitors." European Journal of Medicinal Chemistry 116 (June 2016): 59–70. http://dx.doi.org/10.1016/j.ejmech.2016.03.066.

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Matthijs, Hans C. P., Jan Maarten Van Steenbergen, and Ruud Kraayenhof. "Studies on 9-amino-6-chloro-2-methoxy acridine fluorescence quenching and enhancement in relation to energy transduction in spheroplasts and intact cells of the cyanobacterium Plectonema boryanum." Photosynthesis Research 7, no. 1 (1985): 59–67. http://dx.doi.org/10.1007/bf00032922.

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8

Golcs, Ádám, Panna Vezse, Bálint Árpád Ádám, Péter Huszthy, and Tünde Tóth. "Comparison in practical applications of crown ether sensor molecules containing an acridone or an acridine unit – a study on protonation and complex formation." Journal of Inclusion Phenomena and Macrocyclic Chemistry 101, no. 1-2 (2021): 63–75. http://dx.doi.org/10.1007/s10847-021-01086-2.

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AbstractCrown ethers containing an acridone or an acridine unit are successfully applied opto- and electrochemical cation sensors. The heteroaromatic unit of these macrocycles can be in different forms during the applications, which have a strong influence on the sensing behavior. Moreover, in the case of acridono-macrocycles a prototropic equilibrium takes place upon complexation, which is effected by the physicochemical characteristics. A Pb2+-selective acridono-18-crown-6 ether and its 9-phenylacridino-analogue were used as model compounds for comparing the different forms of the heterocycl
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9

Di Giorgio, Carole, Florence Delmas, Nathalie Filloux, et al. "In Vitro Activities of 7-Substituted 9-Chloro and 9-Amino-2-Methoxyacridines and Their Bis- and Tetra-Acridine Complexes against Leishmania infantum." Antimicrobial Agents and Chemotherapy 47, no. 1 (2003): 174–80. http://dx.doi.org/10.1128/aac.47.1.174-180.2003.

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ABSTRACT 9-Chloro and 9-amino-2-methoxyacridines bearing different substituents in position 7, as well as their corresponding unsubstituted dimeric and tetrameric complexes, were investigated for in vitro antiproliferative properties against Leishmania infantum compared to toxicity towards human monocytes. The results clearly confirmed that several compounds of the 2-methoxyacridine series, together with their corresponding dimeric and tetrameric derivatives, had strong in vitro antiparasitic properties. Antileishmanial activity was shown to depend on the nature of both 7- and 9-substituted gr
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10

Kitchen, S. E., Yuehhwa Wang, A. L. Baumstark, W. D. Wilson, and David W. Boykin. "The intercalation of 6-chloro-2-substituted-9-[[3-(dimethylamino)propyl]amino]acridines with DNA." Journal of Medicinal Chemistry 28, no. 7 (1985): 940–44. http://dx.doi.org/10.1021/jm00145a016.

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Dissertations / Theses on the topic "Acridine(amino-9 chloro-6 methoxy-2)"

1

Sun, Jian-Sheng. "Etats excites et relaxation de la 2-methoxy,6-chloro,9-aminoacridine : interactions d'oligonucleotides lies a la 2-methoxy,6-chloro,9-aminoacridine et d'acides nucleiques." Paris 6, 1987. http://www.theses.fr/1987PA066634.

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Demonchaux, Patrice. "Recherche d'agents radioprotecteurs : synthèse et mécanisme d'action de composés de type intercalant-aminothiol." Grenoble 1, 1988. http://www.theses.fr/1988GRE10016.

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Les intercalants utilises sont des amino-9 chloro-6 methoxy-2 acridines des amino-4 chloro-7 quinoleines et des amino-4 chloro-7 methyl-1 quinoleiniums sur lesquels ont ete introduites des chaines analogues a celles de la cysteamine et du wr 2727; etude de l'affinite de ces composes avec l'adn
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3

Jayat-Vignoles, Chantal. "Caractérisation de la 3-amino-6-méthoxy-9 (2-hydroxyéthylamine) acridine pour l'étude du compartiment nucléaire." Limoges, 1992. http://www.theses.fr/1992LIMO0174.

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Mangueira, Vivianne Mendes. "Estudo da toxicidade e atividade antitumoral do derivado acridínico n’-(2-cloro-6-metoxi-acridin-9-yl)-2-ciano-3-(4-dimetilaminofenil)-acrilohidrazida em modelo experimental de tumor ascítico de ehrlich." Universidade Federal da Paraíba, 2015. http://tede.biblioteca.ufpb.br:8080/handle/tede/8821.

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