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PUBMED FOR HANDHELDS

Journal Abstract Search


159 related items for PubMed ID: 15935900

  • 1. Epoxide-containing side chains enhance antiproliferative activity of paullones.
    Xie X, Lemcke T, Gussio R, Zaharevitz DW, Leost M, Meijer L, Kunick C.
    Eur J Med Chem; 2005 Jul; 40(7):655-61. PubMed ID: 15935900
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  • 4. Indolobenzazepin-7-ones and 6-, 8-, and 9-membered ring derivatives as tubulin polymerization inhibitors: synthesis and structure--activity relationship studies.
    Putey A, Popowycz F, Do QT, Bernard P, Talapatra SK, Kozielski F, Galmarini CM, Joseph B.
    J Med Chem; 2009 Oct 08; 52(19):5916-25. PubMed ID: 19743863
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  • 6. 4- and 5-aroylindoles as novel classes of potent antitubulin agents.
    Liou JP, Wu CY, Hsieh HP, Chang CY, Chen CM, Kuo CC, Chang JY.
    J Med Chem; 2007 Sep 06; 50(18):4548-52. PubMed ID: 17685504
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  • 7. Synthesis and antiproliferative activities of isoindigo and azaisoindigo derivatives.
    Bouchikhi F, Anizon F, Moreau P.
    Eur J Med Chem; 2008 Apr 06; 43(4):755-62. PubMed ID: 17628214
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  • 9. Synthesis and evaluation of novel 7-azaindazolyl-indolyl-maleimide derivatives as antitumor agents and protein kinase C inhibitors.
    Ye Q, Cao J, Zhou X, Lv D, He Q, Yang B, Hu Y.
    Bioorg Med Chem; 2009 Jul 01; 17(13):4763-72. PubMed ID: 19447039
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  • 11. Synthesis, kinase inhibitory potencies and in vitro antiproliferative activity of isoindigo and 7'-azaisoindigo derivatives substituted by Sonogashira cross-coupling.
    Bouchikhi F, Anizon F, Moreau P.
    Eur J Med Chem; 2009 Jun 01; 44(6):2705-10. PubMed ID: 19232788
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  • 12. Design, synthesis and structure-activity relationships of antiproliferative 1,3-disubstituted urea derivatives.
    Li HQ, Zhu TT, Yan T, Luo Y, Zhu HL.
    Eur J Med Chem; 2009 Feb 01; 44(2):453-9. PubMed ID: 18514972
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  • 14. Antitumor pyrido[3,2-d][1]benzazepines: synthesis and in vitro activity of thiophene analogs.
    Link A, Zaharevitz DW, Kunick C.
    Pharmazie; 1999 Mar 01; 54(3):163-6. PubMed ID: 10192102
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  • 16. Matrix compare analysis discriminates subtle structural differences in a family of novel antiproliferative agents, diaryl-3-hydroxy-2,3,3a,10a-tetrahydrobenzo[b]cycylopenta[e]azepine-4,10(1H,5H)-diones.
    Kunick C, Bleeker C, Prühs C, Totzke F, Schächtele C, Kubbutat MH, Link A.
    Bioorg Med Chem Lett; 2006 Apr 15; 16(8):2148-53. PubMed ID: 16464582
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  • 19. d-Fused [1]benzazepines with selective in vitro antitumor activity: synthesis and structure-activity relationships.
    Link A, Kunick C.
    J Med Chem; 1998 Apr 09; 41(8):1299-305. PubMed ID: 9548819
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