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Journal Abstract Search

118 related items for PubMed ID: 24939105

  • 1. Design, synthesis and biological evaluation of naphthostyril derivatives as novel protein kinase FGFR1 inhibitors.
    Gryshchenko AA, Levchenko KV, Bdzhola VG, Ruban TP, Lukash LL, Yarmoluk SM.
    J Enzyme Inhib Med Chem; 2015 Feb; 30(1):126-32. PubMed ID: 24939105
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  • 3. In vitro anticancer screening and radiosensitizing evaluation of some new quinolines and pyrimido[4,5-b]quinolines bearing a sulfonamide moiety.
    Ghorab MM, Ragab FA, Heiba HI, Arafa RK, El-Hossary EM.
    Eur J Med Chem; 2010 Sep; 45(9):3677-84. PubMed ID: 20684857
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  • 5. Design, synthesis and biological evaluation of 4-bromo-N-(3,5-dimethoxyphenyl)benzamide derivatives as novel FGFR1 inhibitors for treatment of non-small cell lung cancer.
    Xie Z, Cheng D, Luo L, Shen G, Pan S, Pan Y, Chen B, Wang X, Liu Z, Zhang Y, Ye F.
    J Enzyme Inhib Med Chem; 2018 Dec; 33(1):905-919. PubMed ID: 29734851
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  • 6. Novel pyridinyl and pyrimidinylcarbazole sulfonamides as antiproliferative agents.
    Hu L, Li ZR, Wang YM, Wu Y, Jiang JD, Boykin DW.
    Bioorg Med Chem Lett; 2007 Mar 01; 17(5):1193-6. PubMed ID: 17197178
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  • 7. Synthesis and in vitro anticancer evaluation of some novel hexahydroquinoline derivatives having a benzenesulfonamide moiety.
    Al-Said MS, Ghorab MM, Al-Dosari MS, Hamed MM.
    Eur J Med Chem; 2011 Jan 01; 46(1):201-7. PubMed ID: 21112675
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  • 8. Design, synthesis, and antitumor screening of certain novel tetrahydroquinoline sulfonamides.
    Alafeefy AM.
    J Enzyme Inhib Med Chem; 2015 Apr 01; 30(2):189-94. PubMed ID: 24666309
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  • 9. Design, synthesis, and biological evaluation of novel N-γ-carboline arylsulfonamides as anticancer agents.
    Chen J, Liu T, Wu R, Lou J, Cao J, Dong X, Yang B, He Q, Hu Y.
    Bioorg Med Chem; 2010 Dec 15; 18(24):8478-84. PubMed ID: 21067933
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  • 12. Synthesis and kinase inhibitory activity of new sulfonamide derivatives of pyrazolo[4,3-e][1,2,4]triazines.
    Mojzych M, Šubertová V, Bielawska A, Bielawski K, Bazgier V, Berka K, Gucký T, Fornal E, Kryštof V.
    Eur J Med Chem; 2014 May 06; 78():217-24. PubMed ID: 24681986
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  • 14. Synthesis, structural characterization, and in vitro antitumor activity of novel N-(6-chloro-1,1-dioxo-1,4,2-benzodithiazin-3-yl)arylsulfonamides.
    Brzozowski Z, Saczewski F, Sławiński J, Bednarski PJ, Grünert R, Gdaniec M.
    Bioorg Med Chem; 2007 Apr 01; 15(7):2560-72. PubMed ID: 17306551
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  • 17. Synthesis and biological evaluation of 4-phenoxy-6,7-disubstituted quinolines possessing semicarbazone scaffolds as selective c-Met inhibitors.
    Qi B, Tao H, Wu D, Bai J, Shi Y, Gong P.
    Arch Pharm (Weinheim); 2013 Aug 01; 346(8):596-609. PubMed ID: 23843304
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  • 18. Synthesis, in-vitro anticancer screening and radiosensitizing evaluation of some new N-(quinoxalin-2-yl)benzenesulfonamide derivatives.
    Ghorab MM, Ragab FA, Heiba HI, El-Gazzar MG, El-Gazzar MG.
    Arzneimittelforschung; 2012 Jan 01; 62(1):46-52. PubMed ID: 22331763
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  • 19. Design, Synthesis, and Biological Evaluation of C-2 Substituted 3Hthieno[ 2,3-d]pyrimidin-4-one Derivatives as Novel FGFR1 Inhibitors.
    Guo P, Xie Z, Zhang H, Zhang Z, Han C, Cheng D, Lin D, Zhang Y, Wang X, Guo X, Ye F.
    Med Chem; 2017 Jan 01; 13(8):753-760. PubMed ID: 28641527
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  • 20. Acenaphtho[1,2-b]pyrrole-based selective fibroblast growth factor receptors 1 (FGFR1) inhibitors: design, synthesis, and biological activity.
    Chen Z, Wang X, Zhu W, Cao X, Tong L, Li H, Xie H, Xu Y, Tan S, Kuang D, Ding J, Qian X.
    J Med Chem; 2011 Jun 09; 54(11):3732-45. PubMed ID: 21517068
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