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Journal Abstract Search

326 related items for PubMed ID: 9003520

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  • 4. Synthesis of nitrated indenoisoquinolines as topoisomerase I inhibitors.
    Morrell A, Antony S, Kohlhagen G, Pommier Y, Cushman M.
    Bioorg Med Chem Lett; 2004 Jul 16; 14(14):3659-63. PubMed ID: 15203138
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  • 7. Synthesis, topoisomerase I inhibitory activity and in vitro cytotoxicity of camptothecin derivatives bearing five-membered heterocycle containing 10-substituents.
    Zhao R, Guan LL, Oreski B, Lown JW.
    Anticancer Drug Des; 1998 Mar 16; 13(2):145-57. PubMed ID: 9524556
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  • 9. In vivo antitumor activity of two new seven-substituted water-soluble camptothecin analogues.
    Emerson DL, Besterman JM, Brown HR, Evans MG, Leitner PP, Luzzio MJ, Shaffer JE, Sternbach DD, Uehling D, Vuong A.
    Cancer Res; 1995 Feb 01; 55(3):603-9. PubMed ID: 7834631
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  • 10. Design, synthesis and topoisomerase II inhibition activity of 4'-demethylepipodophyllotoxin-lexitropsin conjugates.
    Gupta R, al-Said NH, Oreski B, Lown JW.
    Anticancer Drug Des; 1996 Jun 01; 11(4):325-38. PubMed ID: 8679055
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  • 11. Differential effects of the poly (ADP-ribose) polymerase (PARP) inhibitor NU1025 on topoisomerase I and II inhibitor cytotoxicity in L1210 cells in vitro.
    Bowman KJ, Newell DR, Calvert AH, Curtin NJ.
    Br J Cancer; 2001 Jan 05; 84(1):106-12. PubMed ID: 11139322
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  • 14. [Synthesis of camptothecin glycosides by phase transfer-catalysis and its inhibitory activity against topo I].
    Li QY, Zhang Y, Yao LP, Fu YJ, Zu YG, Chen XQ, Zheng CY.
    Yao Xue Xue Bao; 2005 Dec 05; 40(12):1116-21. PubMed ID: 16496676
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  • 15. Synthesis and antitumor activity of novel 10-substituted camptothecin analogues.
    Li Q, Zu Y, Shi R, Yao L, Fu Y, Yang Z, Li L.
    Bioorg Med Chem; 2006 Nov 01; 14(21):7175-82. PubMed ID: 16870453
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  • 16. Synthesis and cytotoxic activity of new 9-substituted camptothecins.
    Dallavalle S, Rocchetta DG, Musso L, Merlini L, Morini G, Penco S, Tinelli S, Beretta GL, Zunino F.
    Bioorg Med Chem Lett; 2008 May 01; 18(9):2781-7. PubMed ID: 18434153
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  • 17. Novel stable camptothecin derivatives replacing the E-ring lactone by a ketone function are potent inhibitors of topoisomerase I and promising antitumor drugs.
    Lansiaux A, Léonce S, Kraus-Berthier L, Bal-Mahieu C, Mazinghien R, Didier S, David-Cordonnier MH, Hautefaye P, Lavielle G, Bailly C, Hickman JA, Pierré A.
    Mol Pharmacol; 2007 Aug 01; 72(2):311-9. PubMed ID: 17494837
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  • 18. Water soluble inhibitors of topoisomerase I: quaternary salt derivatives of camptothecin.
    Lackey K, Sternbach DD, Croom DK, Emerson DL, Evans MG, Leitner PL, Luzzio MJ, McIntyre G, Vuong A, Yates J, Besterman JM.
    J Med Chem; 1996 Feb 02; 39(3):713-9. PubMed ID: 8576914
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  • 19. Identification of mutations at DNA topoisomerase I responsible for camptothecin resistance.
    Wang LF, Ting CY, Lo CK, Su JS, Mickley LA, Fojo AT, Whang-Peng J, Hwang J.
    Cancer Res; 1997 Apr 15; 57(8):1516-22. PubMed ID: 9108454
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