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Journal articles on the topic 'Ellipticine – Analogues'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Meesala, Ramu, Mohammed Ezzat, Mohd Mordi, and Sharif Mansor. "Synthesis of Novel Pyridocarbazoles Analogues of Ellipticine." Synlett 25, no. 15 (2014): 2176–78. http://dx.doi.org/10.1055/s-0034-1378518.

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2

Kibal'nyi, A. V., O. I. Kharaneko, and V. I. Dulenko. "ChemInform Abstract: New Approach to Ellipticine Analogues." ChemInform 33, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.200232145.

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3

K. Pandit, Upendra, Willem F. A. Wijsmuller, Martin J. Wanner, and Gerrit-Jan Koomen. "Pyridocarbazole Alkaloids. Synthesis of Olivacine and Ellipticine Analogues." HETEROCYCLES 24, no. 7 (1986): 1795. http://dx.doi.org/10.3987/r-1986-07-1795.

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4

Chabane, Hadjila, Christelle Lamazzi, Valérie Thiéry, Gérald Guillaumet, and Thierry Besson. "Synthesis of novel 2-cyanothiazolocarbazoles analogues of ellipticine." Tetrahedron Letters 43, no. 14 (2002): 2483–86. http://dx.doi.org/10.1016/s0040-4039(02)00353-2.

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5

Sha, Chin-Kang, and Jeng-Fenn Yang. "Total syntheses of ellipticine alkaloids and their amino analogues." Tetrahedron 48, no. 48 (1992): 10645–54. http://dx.doi.org/10.1016/s0040-4020(01)88360-5.

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6

Meesala, Ramu, Mohammed Oday Ezzat, Mohd Nizam Mordi, and Sharif Mahsufi Mansor. "ChemInform Abstract: Synthesis of Novel Pyridocarbazoles Analogues of Ellipticine." ChemInform 46, no. 10 (2015): no. http://dx.doi.org/10.1002/chin.201510213.

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7

Mousset, Deborah, Rémi Rabot, Pascal Bouyssou, Gérard Coudert, and Isabelle Gillaizeau. "Synthesis and biological evaluation of novel benzoxazinic analogues of ellipticine." Tetrahedron Letters 51, no. 30 (2010): 3987–90. http://dx.doi.org/10.1016/j.tetlet.2010.05.123.

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8

Chabane, Hadjila, Christelle Lamazzi, Valerie Thiery, Gerald Guillaumet, and Thierry Besson. "ChemInform Abstract: Synthesis of Novel 2-Cyanothiazolocarbazole Analogues of Ellipticine." ChemInform 33, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.200228267.

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9

Ferlin, Maria Grazia, Christine Marzano, Valentina Gandin, Stefano Dall'Acqua, and Lisa Dalla Via. "DNA Binding Ellipticine Analogues: Synthesis, Biological Evaluation, and Structure-Activity Relationships." ChemMedChem 4, no. 3 (2009): 363–77. http://dx.doi.org/10.1002/cmdc.200800368.

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10

FERLIN, M. G., G. CHIARELOTTO, C. MARZANO, S. MOBILIO, F. CARLASSARE, and F. BACCICHETTI. "ChemInform Abstract: Antiproliferative Activity of Some Unsubstituted Angular Analogues of Ellipticine." ChemInform 26, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.199531222.

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11

SHA, C. K., and J. F. YANG. "ChemInform Abstract: Total Syntheses of Ellipticine Alkaloids and Their Amino Analogues." ChemInform 24, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199313278.

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12

Tran-Thi, Hong Anh, Thuan Nguyen-Thi, Sylvie Michel, et al. "Synthesis and Cytotoxic Activity of Pyranocarbazole Analogues of Ellipticine and Acronycine." CHEMICAL & PHARMACEUTICAL BULLETIN 52, no. 5 (2004): 540–45. http://dx.doi.org/10.1248/cpb.52.540.

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13

Peixoto, Fernanda M. C., Maria-Joa˜o R. P. Queiroz, and Gilbert Kirsch. "Synthesis of Precursors of Linear Thienocarbazole Analogues of Ellipticine and Olivacine." Journal of Chemical Research, no. 4 (1998): 172–73. http://dx.doi.org/10.1039/a705628a.

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14

Hamed, Atef A. "Some Reactions of 3-Chloroisoindolium Salts with Nucleophiles: Access to Isoindole Derivatives and Ellipticine Analogues as Potential Antiviral Agents." Journal of Chemical Research 2005, no. 1 (2005): 54–58. http://dx.doi.org/10.3184/0308234053431121.

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3-Chloro-2-substituted-1-oxoisoindolium hexachloroantimonate (1) reacted with water, ethanol and dimethyl-cyanamide to give the corresponding phthalimide derivatives 2, 3 and 4 respectively. Reaction of 1a with nitriles afforded the intermediate 2-azoniaallene salts 5 which underwent cyclisation reaction upon heating to furnish the ellipticine analogues 6. The biological activities of 6a–e against HIV-1 and HBV viruses were determined.

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15

Timári, Géza, Tibor Soós, György Hajós, András Messmer, János Nacsa, and József Molnár. "Synthesis of novel ellipticine analogues and their inhibition of Moloney leukaemia reverse transcriptase." Bioorganic & Medicinal Chemistry Letters 6, no. 23 (1996): 2831–36. http://dx.doi.org/10.1016/s0960-894x(96)00521-5.

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16

Peixoto, Fernanda M. C., Maria-Joao R. P. Queiroz, and Gilbert Kirsch. "ChemInform Abstract: Synthesis of Precursors of Linear Thienocarbazole Analogues of Ellipticine and Olivacine." ChemInform 30, no. 15 (2010): no. http://dx.doi.org/10.1002/chin.199915139.

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17

TIMARI, G., T. SOOS, G. HAJOS, A. MESSMER, J. NACSA, and J. MOLNAR. "ChemInform Abstract: Synthesis of Novel Ellipticine Analogues and Their Inhibition of Moloney Leukaemia Reverse Transcriptase." ChemInform 28, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.199716182.

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18

Carvalho, A. C. M., and B. Laks. "Investigation of geometry and some electronic properties of AZA analogues of the ellipticine and olivacine derivatives." Journal of Molecular Structure: THEOCHEM 539, no. 1-3 (2001): 273–78. http://dx.doi.org/10.1016/s0166-1280(00)00797-1.

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19

Yang, Chunhao, Yuyuan Xie, and Yanhong Chen. "Synthesis of 4-Azachromeno[2,3-b]indol-11(6H)-one and Its Derivatives as Analogues of Ellipticine." HETEROCYCLES 80, no. 1 (2010): 251. http://dx.doi.org/10.3987/com-08-s(s)3.

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20

Sharples, Derek, György Hajós, Zsuzsanna Riedl, Dorottya Csányi, József Molnár, and Diana Szabó. "Ellipticine analogues and related compounds as inhibitors of reverse transcriptase and as inhibitors of the efflux pump." Archiv der Pharmazie 334, no. 8-9 (2001): 269. http://dx.doi.org/10.1002/1521-4184(200109)334:8/9<269::aid-ardp269>3.0.co;2-#.

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21

Shi, Leming M., Yi Fan, Timothy G. Myers, et al. "Mining the NCI Anticancer Drug Discovery Databases: Genetic Function Approximation for the QSAR Study of Anticancer Ellipticine Analogues." Journal of Chemical Information and Computer Sciences 38, no. 2 (1998): 189–99. http://dx.doi.org/10.1021/ci970085w.

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22

Zhang, Quan, Chongsheng Shi, Hai-Ren Zhang, and Kung K. Wang. "Synthesis of 6H-Indolo[2,3-b][1,6]naphthyridines and Related Compounds as the 5-Aza Analogues of Ellipticine Alkaloids." Journal of Organic Chemistry 65, no. 23 (2000): 7977–83. http://dx.doi.org/10.1021/jo000978e.

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23

Chen, Yanhong, Chunhao Yang, and Yuyuan Xie. "ChemInform Abstract: Synthesis of 4-Azachromeno[2,3-b]indol-11(6H)-one and Its Derivatives as Analogues of Ellipticine." ChemInform 41, no. 21 (2010): no. http://dx.doi.org/10.1002/chin.201021153.

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24

Jones, R. Alan, Joachim Pastor, Jorge Siro, and Tevita N. Voro. "Pyrroloindole analogues of ellipticine. The synthesis and DNA intercalative properties of 5,10-dihyhdro-5,10,dimethyl-2,5,10-triazadibenzo[a,e]pentalene." Tetrahedron 53, no. 2 (1997): 479–86. http://dx.doi.org/10.1016/s0040-4020(96)00994-5.

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25

Praly-Deprez, Isabelle, Christian Rivalle, Jean Belehradek, Christians Huel, and Emile Bisagni. "Synthesis of 11-amino-substituted-5,6-dimethyl-5H-pyrido[3′,4′:4,5]pyrrolo-[2,3-g]isoquinolines as new ellipticine analogues." J. Chem. Soc., Perkin Trans. 1, no. 12 (1991): 3173–75. http://dx.doi.org/10.1039/p19910003173.

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26

SHI, L. M., Y. FAN, T. G. MYERS, et al. "ChemInform Abstract: Mining the NCI Anticancer Drug Discovery Databases: Genetic Function Approximation for the QSAR Study of Anticancer Ellipticine Analogues." ChemInform 29, no. 27 (2010): no. http://dx.doi.org/10.1002/chin.199827312.

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27

ANDERSON, W. K., A. GOPALSAMY, and P. S. REDDY. "ChemInform Abstract: Design, Synthesis, and Study of 9-Substituted Ellipticine and 2- Methylellipticinium Analogues as Potential CNS-Selective Antitumor Agents." ChemInform 25, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.199450157.

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28

Zhang, Quan, Chongsheng Shi, Hai-Ren Zhang, and Kung K. Wang. "ChemInform Abstract: Synthesis of 6H-Indolo[2,3-b][1,6]naphthyridines and Related Compounds as the 5-Aza Analogues of Ellipticine Alkaloids." ChemInform 32, no. 12 (2001): no. http://dx.doi.org/10.1002/chin.200112204.

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29

PRALY-DEPREZ, I., C. RIVALLE, J. BELEHRADEK, C. HUEL, and E. BISAGNI. "ChemInform Abstract: Synthesis of 11-Amino-Substituted-5,6-dimethyl-5H-pyrido(3′,4′:4,5) pyrrolo(2,3-g)isoquinolines as New Ellipticine Analogues." ChemInform 23, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199213223.

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30

JONES, R. A., J. PASTOR, J. SIRO, and T. N. VORO. "ChemInform Abstract: Pyrroloindole Analogues of Ellipticine. The Synthesis and DNA Intercalative Properties of 5,10-Dihydro-5,10-dimethyl-2,5,10- triazadibenzo(a,e)pentalene." ChemInform 28, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199718152.

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31

Mathé, G., E. Chenu, C. Bourut, and S. Orbach-Arbouys. "The in vivo effect of ellipticine analogues on the blood concentration of Friend virus: a murine model for studying anti-HIV drugs." Biomedicine & Pharmacotherapy 47, no. 10 (1993): 457–60. http://dx.doi.org/10.1016/0753-3322(93)90343-j.

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32

Vilarem, M. J., J. F. Riou, E. Multon, M. P. Gras, and C. J. Larsen. "The in vitro involvement of topoisomerase II in the activity of aza-ellipticine analogues is not correlated with drug activity on isolated nuclei." Biochemical Pharmacology 35, no. 13 (1986): 2087–95. http://dx.doi.org/10.1016/0006-2952(86)90575-7.

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33

GRIBBLE, G. W., M. G. SAULNIER, J. A. OBAZA-NUTAITIS, and D. M. KETCHA. "ChemInform Abstract: A Versatile and Efficient Construction of the 6H-Pyrido(4,3-b) carbazole Ring System. Syntheses of the Antitumor Alkaloids Ellipticine, 9-Methoxyellipticine, and Olivacine and Their Analogues." ChemInform 24, no. 9 (2010): no. http://dx.doi.org/10.1002/chin.199309242.

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34

Márquez, Edgar, José R. Mora, Virginia Flores-Morales, Daniel Insuasty, and Luis Calle. "Modeling the Antileukemia Activity of Ellipticine-Related Compounds: QSAR and Molecular Docking Study." Molecules 25, no. 1 (2019): 24. http://dx.doi.org/10.3390/molecules25010024.

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The antileukemia cancer activity of organic compounds analogous to ellipticine representes a critical endpoint in the understanding of this dramatic disease. A molecular modeling simulation on a dataset of 23 compounds, all of which comply with Lipinski’s rules and have a structure analogous to ellipticine, was performed using the quantitative structure activity relationship (QSAR) technique, followed by a detailed docking study on three different proteins significantly involved in this disease (PDB IDs: SYK, PI3K and BTK). As a result, a model with only four descriptors (HOMO, softness, AC1RA

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35

Dari, Abdelmjid, Léon E. Christiaens, Marcel J. Renson, et al. "Synthesis of a Selenium Analogue of Ellipticine: 5,11-dimethyl[1]benzoselenolo[2,3-g]isoquinoline." Acta Chemica Scandinavica 47 (1993): 208–11. http://dx.doi.org/10.3891/acta.chem.scand.47-0208.

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36

DARI, A., L. E. CHRISTIAENS, and M. J. RENSON. "ChemInform Abstract: Synthesis of a Selenium Analogue of Ellipticine: 5,11-Dimethyl(1) benzoselenolo(2,3-g)isoquinoline." ChemInform 24, no. 20 (2010): no. http://dx.doi.org/10.1002/chin.199320272.

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37

Bisagni, Emile, Marilys Rautureau, and Christiane Huel. "1-Functionalized 5,6-Dimethyl-6H-pyrido[4,3-b]carbazoles (Ellipticines) and Analogues: A New Rapid Synthesis." HETEROCYCLES 27, no. 7 (1988): 1671. http://dx.doi.org/10.3987/com-88-4543.

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38

GURZADYAN, V. G., P. A. R. ADE, P. De BERNARDIS, et al. "ELLIPTICITY ANALYSIS OF THE BOOMERanG CMB MAPS." International Journal of Modern Physics D 12, no. 10 (2003): 1859–73. http://dx.doi.org/10.1142/s0218271803004419.

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The properties of the Cosmic Microwave Background (CMB) maps carry valuable cosmological information. Here we report the results of the analysis hot and cold CMB anisotropy spots in the BOOMERanG 150 GHz map in terms of number, area, ellipticity, vs. temperature threshold. We carried out this analysis for the map obtained by summing independent measurement channels (signal plus noise map) and for a comparison map (noise only map) obtained by differencing the same channels. The anisotropy areas (spots) have been identified for both maps for various temperature thresholds and a catalog of the sp

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39

CHUNCHATPRASERT, L., P. DHARMASENA, A. M. F. OLIVEIRA-CAMPOS, M. J. R. P. QUEIROZ, M. M. M. RAPOSO, and P. V. R. SHANNON. "ChemInform Abstract: Anti-Tumour Heterocycles. Part 13. The Syntheses of Two New Pyridocarbazoles (Ellipticines) and Some Pyrrolocarbazole Analogues." ChemInform 27, no. 30 (2010): no. http://dx.doi.org/10.1002/chin.199630280.

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40

Bisagni, Emile, and Nguyen Chi Hung. "Premiere synthese de methyl-4-5h- pyrido ¦3',4':4,5¦pyrrolo ¦3,2-c¦pyridines, analogues tricycliques des aza-9 ellipticines." Tetrahedron 42, no. 8 (1986): 2311–18. http://dx.doi.org/10.1016/s0040-4020(01)90611-8.

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41

Fossé, Philippe, Brigitte René, Jean-Marie Saucier, Chi Hung Nguyen, Emile Bisagni та Claude Paoletti. "Stimulation by γ-carboline derivatives (simplified analogues of antitumor ellipticines) of site specific DNA cleavage by calf DNA topoisomerase II". Biochemical Pharmacology 39, № 4 (1990): 669–76. http://dx.doi.org/10.1016/0006-2952(90)90144-a.

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42

Garetto, Claudia, and Günther Hörmann. "MICROLOCAL ANALYSIS OF GENERALIZED FUNCTIONS: PSEUDODIFFERENTIAL TECHNIQUES AND PROPAGATION OF SINGULARITIES." Proceedings of the Edinburgh Mathematical Society 48, no. 3 (2005): 603–29. http://dx.doi.org/10.1017/s0013091504000148.

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AbstractWe characterize microlocal regularity, in the $\mathcal{G}^{\infty}$-sense, of Colombeau generalized functions by an appropriate extension of the classical notion of micro-ellipticity to pseudodifferential operators with slow-scale generalized symbols. Thus we obtain an alternative, yet equivalent, way of determining generalized wavefront sets that is analogous to the original definition of the wavefront set of distributions via intersections over characteristic sets. The new methods are then applied to regularity theory of generalized solutions of (pseudo)differential equations, where

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43

Schleicher, Jörg, and Rafael Aleixo. "Time and depth remigration in elliptically anisotropic media using image-wave propagation." GEOPHYSICS 72, no. 1 (2007): S1—S9. http://dx.doi.org/10.1190/1.2374857.

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The image-wave equations for the problems of depth and time remigration in elliptically anisotropic media are second-order partial differential equations similar to the acoustic-wave equation. The propagation variable is the vertical velocity or the medium ellipticity rather than time. These differential equations are derived from the kinematic properties of anisotropic remigration. The objective is to construct subsurface images that correspond to different vertical velocity and/or different degrees of medium anisotropy directly from a single migrated image. In this way, anisotropy panels can

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44

Voitovych, Mykhailo. "Continuity of weak solutions to nonlinear fourth-order equations with strengthened ellipticity via Wolff potentials." Proceedings of the Institute of Applied Mathematics and Mechanics NAS of Ukraine 33 (December 27, 2019): 33–49. http://dx.doi.org/10.37069/1683-4720-2019-33-3.

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In the present article nonlinear fourth-order equations in the divergence form with L^1-right-hand sides and the strengthened ellipticity condition on the coefficients are analyzed. Such equations, but with sufficiently regular right-hand sides, first appeared in the works of Professor I.V. Skrypnik concerning the regularity of generalized solutions for multidimensional nonlinear elliptic equations of high order. This class of equations correctly generalizes the corresponding nonlinear second-order elliptic equations with non-standard growth conditions on the coefficients, which are models for

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45

Miki, Yasuyoshi, Noriko Nakamura, Ryota Yamakawa, Hajime Hibino, Hiroko Hachiken, and Ko-ichi Matsushita. "ChemInform Abstract: Reaction of 3-Ethoxycarbonylindolizine-1,2-dicarboxylic Anhydride with (3-Bromo-4-pyridyl)triisopropoxytitanium: Synthesis of 5,12-Dimethylindolizino[2,1-g]isoquinoline (Ellipticine Analogue)." ChemInform 32, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.200107193.

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46

Goddard, J. D., та Jaesung Lee. "On the stability of the μ(I) rheology for granular flow". Journal of Fluid Mechanics 833 (3 листопада 2017): 302–31. http://dx.doi.org/10.1017/jfm.2017.651.

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This article deals with the Hadamard instability of the so-called$\unicode[STIX]{x1D707}(I)$model of dense rapidly sheared granular flow, as reported recently by Barkeret al.(J. Fluid Mech., vol. 779, 2015, pp. 794–818). The present paper presents a more comprehensive study of the linear stability of planar simple shearing and pure shearing flows, with account taken of convective Kelvin wavevector stretching by the base flow. We provide a closed-form solution for the linear-stability problem and show that wavevector stretching leads to asymptotic stabilization of the non-convective instability

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47

DORMOY, J. R., and A. HEYMES. "ChemInform Abstract: Industrial Synthesis of Ellipticines. Part 2. Elaboration of a Novel Route to 6H-Pyrido(4,3-b)carbazoles and Analogues. Part B. Synthesis of Tetracyclic Structures." ChemInform 24, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199332244.

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48

Denzel, Philipp, Sampath Mukherjee, Jonathan P. Coles, and Prasenjit Saha. "Lessons from a blind study of simulated lenses: image reconstructions do not always reproduce true convergence." Monthly Notices of the Royal Astronomical Society 492, no. 3 (2020): 3885–903. http://dx.doi.org/10.1093/mnras/staa108.

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ABSTRACT In the coming years, strong gravitational lens discoveries are expected to increase in frequency by two orders of magnitude. Lens-modelling techniques are being developed to prepare for the coming massive influx of new lens data, and blind tests of lens reconstruction with simulated data are needed for validation. In this paper, we present a systematic blind study of a sample of 15 simulated strong gravitational lenses from the EAGLE suite of hydrodynamic simulations. We model these lenses with a free-form technique and evaluate reconstructed mass distributions using criteria based on

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49

Mathé, G., P. Pontiggia, C. Bourut, E. Chenu, and S. Orbach-Arbouys. "In vivo eradication of Friend virus as an experimental HIV-model, by combination of zidovudine, acriflavine and an ellipticine analogue. Possible application to the treatment of human pre-AIDS?" Biomedicine & Pharmacotherapy 48, no. 2 (1994): 51–53. http://dx.doi.org/10.1016/0753-3322(94)90075-2.

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50

DORMOY, J. R., and A. HEYMES. "ChemInform Abstract: Industrial Synthesis of Ellipticines. Part 1. Elaboration of a Novel Route to 6H-Pyrido(4,3-b)carbazoles and Analogues. Part A. Synthesis and Study of the Precursors." ChemInform 24, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199332243.

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