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PUBMED FOR HANDHELDS

Journal Abstract Search


281 related items for PubMed ID: 9822546

  • 21. Synthesis and evaluation of 3-aryloxymethyl-1,2-dimethylindole-4,7-diones as mechanism-based inhibitors of NAD(P)H:quinone oxidoreductase 1 (NQO1) activity.
    Colucci MA, Reigan P, Siegel D, Chilloux A, Ross D, Moody CJ.
    J Med Chem; 2007 Nov 15; 50(23):5780-9. PubMed ID: 17944451
    [Abstract] [Full Text] [Related]

  • 22. NAD(P)H:quinone oxidoreductase-1-dependent and -independent cytotoxicity of potent quinone Cdc25 phosphatase inhibitors.
    Han Y, Shen H, Carr BI, Wipf P, Lazo JS, Pan SS.
    J Pharmacol Exp Ther; 2004 Apr 15; 309(1):64-70. PubMed ID: 14718602
    [Abstract] [Full Text] [Related]

  • 23. Lavendamycin antitumor agents: structure-based design, synthesis, and NAD(P)H:quinone oxidoreductase 1 (NQO1) model validation with molecular docking and biological studies.
    Hassani M, Cai W, Koelsch KH, Holley DC, Rose AS, Olang F, Lineswala JP, Holloway WG, Gerdes JM, Behforouz M, Beall HD.
    J Med Chem; 2008 Jun 12; 51(11):3104-15. PubMed ID: 18457384
    [Abstract] [Full Text] [Related]

  • 24. Betulin-1,4-quinone hybrids: Synthesis, anticancer activity and molecular docking study with NQO1 enzyme.
    Kadela-Tomanek M, Bębenek E, Chrobak E, Marciniec K, Latocha M, Kuśmierz D, Jastrzębska M, Boryczka S.
    Eur J Med Chem; 2019 Sep 01; 177():302-315. PubMed ID: 31158746
    [Abstract] [Full Text] [Related]

  • 25. Metabolism of bioreductive antitumor compounds by purified rat and human DT-diaphorases.
    Beall HD, Mulcahy RT, Siegel D, Traver RD, Gibson NW, Ross D.
    Cancer Res; 1994 Jun 15; 54(12):3196-201. PubMed ID: 8205540
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  • 27. Studies on quinones. Part 45: novel 7-aminoisoquinoline-5,8-quinone derivatives with antitumor properties on cancer cell lines.
    Valderrama JA, Ibacache JA, Arancibia V, Rodriguez J, Theoduloz C.
    Bioorg Med Chem; 2009 Apr 01; 17(7):2894-901. PubMed ID: 19269832
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  • 31. Studies of pyrrolo[1,2-alpha]benzimidazolequinone DT-diaphorase substrate activity, topoisomerase II inhibition activity, and DNA reductive alkylation.
    Skibo EB, Gordon S, Bess L, Boruah R, Heileman MJ.
    J Med Chem; 1997 Apr 25; 40(9):1327-39. PubMed ID: 9135030
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  • 32. Design, synthesis, and biological evaluation of NAD(P)H: Quinone oxidoreductase (NQO1)-targeted oridonin prodrugs possessing indolequinone moiety for hypoxia-selective activation.
    Xu S, Yao H, Pei L, Hu M, Li D, Qiu Y, Wang G, Wu L, Yao H, Zhu Z, Xu J.
    Eur J Med Chem; 2017 May 26; 132():310-321. PubMed ID: 28395199
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  • 34. Cross-linking and sequence-specific alkylation of DNA by aziridinylquinones. 3. Effects of alkyl substituents.
    Hargreaves RH, O'Hare CC, Hartley JA, Ross D, Butler J.
    J Med Chem; 1999 Jun 17; 42(12):2245-50. PubMed ID: 10377230
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  • 35. Mitomycin C.
    Gibson NW, Ross D.
    Cancer Chemother Biol Response Modif; 1993 Jun 17; 14():45-54. PubMed ID: 8312113
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  • 36. Data mining the NCI cancer cell line compound GI(50) values: identifying quinone subtypes effective against melanoma and leukemia cell classes.
    Marx KA, O'Neil P, Hoffman P, Ujwal ML.
    J Chem Inf Comput Sci; 2003 Jun 17; 43(5):1652-67. PubMed ID: 14502500
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  • 37. Bioactivation of quinones by DT-diaphorase, molecular, biochemical, and chemical studies.
    Ross D, Beall H, Traver RD, Siegel D, Phillips RM, Gibson NW.
    Oncol Res; 1994 Jun 17; 6(10-11):493-500. PubMed ID: 7620217
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  • 38. Kinetics of NAD(P)H:quinone oxidoreductase I (NQO1) inhibition by mitomycin C in vitro and in vivo.
    Gustafson DL, Siegel D, Rastatter JC, Merz AL, Parpal JC, Kepa JK, Ross D, Long ME.
    J Pharmacol Exp Ther; 2003 Jun 17; 305(3):1079-86. PubMed ID: 12649308
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