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Journal Abstract Search

260 related items for PubMed ID: 8141966

  • 1. Synthesis, antitumor evaluation and SAR of new 1H-pyrrolo [3,2-c] quinoline-6,9-diones and 11H-indolo [3,2-c] quinoline-1,4-diones.
    Helissey P, Cros S, Giorgi-Renault S.
    Anticancer Drug Des; 1994 Feb; 9(1):51-67. PubMed ID: 8141966
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  • 2. Heterocyclic quinones. XVI. Pharmacomodulation in the series of 11H-indolo[3,2-c]quinolinediones: synthesis, cytotoxicity and antitumor activity of 3-substituted 11H-pyrido[3',4':4,5]pyrrolo[3,2-c]quinoline-1,4-diones.
    Helissey P, Giorgi-Renault S, Renault J, Cros S.
    Chem Pharm Bull (Tokyo); 1989 Sep; 37(9):2413-6. PubMed ID: 2557983
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  • 3. Heterocyclic quinones. XIV. Pharmacomodulation in a series of 11H-indolo[3,2-c]quinolinediones: synthesis and cytotoxicity of 8-substituted 11H-indolo[3,2-c]quinoline-7,10-diones.
    Helissey P, Giorgi-Renault S, Renault J, Cros S.
    Chem Pharm Bull (Tokyo); 1989 Mar; 37(3):675-9. PubMed ID: 2752476
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  • 4. Investigating the antiproliferative activity of quinoline-5,8-diones and styrylquinolinecarboxylic acids on tumor cell lines.
    Podeszwa B, Niedbala H, Polanski J, Musiol R, Tabak D, Finster J, Serafin K, Milczarek M, Wietrzyk J, Boryczka S, Mol W, Jampilek J, Dohnal J, Kalinowski DS, Richardson DR.
    Bioorg Med Chem Lett; 2007 Nov 15; 17(22):6138-41. PubMed ID: 17904844
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  • 5. Structure-mutagenicity relationships in series of 11H-indolo[3,2-c]quinoline-1,4-diones, tetrahydro-11H-indolo[3,2-c]quinoline-1,4-diones and 11H-pyrido[3',4':4,5]pyrrolo[3,2-c]quinoline-1,4-diones with leukemia cytotoxic properties. Relations with topoisomerase I inhibiting properties.
    Callais F, Helissey P, Min S, Festy B, Giorgi-Renault S.
    Mutat Res; 1994 Nov 01; 311(1):149-56. PubMed ID: 7526168
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  • 6. Synthesis and antiproliferative evaluation of certain indolo[3,2-c]quinoline derivatives.
    Lu CM, Chen YL, Chen HL, Chen CA, Lu PJ, Yang CN, Tzeng CC.
    Bioorg Med Chem; 2010 Mar 01; 18(5):1948-57. PubMed ID: 20171108
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  • 7. [Synthesis and biological activity of new compounds with the 1,3-dioxol(4,5-g)quinoline structure].
    Pellerano C, Savini L.
    Farmaco Sci; 1984 Jul 01; 39(7):640-8. PubMed ID: 6479323
    [Abstract] [Full Text] [Related]

  • 8. Synthesis and antifungal activity of 1H-pyrrolo[3,2-g]quinoline-4,9-diones and 4,9-dioxo-4,9-dihydro-1H-benzo[f]indoles.
    Ryu CK, Lee JY, Jeong SH, Nho JH.
    Bioorg Med Chem Lett; 2009 Jan 01; 19(1):146-8. PubMed ID: 19010669
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  • 14. Synthesis and antitumor evaluation of new thiazolo[5,4-b]quinoline derivatives.
    Alvarez-Ibarra C, Fernández-Granda R, Quiroga ML, Carbonell A, Cárdenas F, Giralt E.
    J Med Chem; 1997 Feb 28; 40(5):668-76. PubMed ID: 9057853
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  • 16. [Research on nitrogen heterocyclic compounds. X. New method of synthesis of pyrrolo/1,2-a/quinoline and its derivatives].
    Vomero S, Chimenti F, Giuliano R, Artico M.
    Farmaco Sci; 1976 Sep 28; 31(9):681-90. PubMed ID: 1010040
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  • 17. Synthesis and antitumoral activity of novel thiazolobenzotriazole, thiazoloindolo[3,2-c]quinoline and quinolinoquinoline derivatives.
    Beauchard A, Jaunet A, Murillo L, Baldeyrou B, Lansiaux A, Chérouvrier JR, Domon L, Picot L, Bailly C, Besson T, Thiéry V.
    Eur J Med Chem; 2009 Oct 28; 44(10):3858-65. PubMed ID: 19427714
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  • 18. Synthesis and anticancer evaluation of certain indolo[2,3-b]quinoline derivatives.
    Chen YL, Hung HM, Lu CM, Li KC, Tzeng CC.
    Bioorg Med Chem; 2004 Dec 15; 12(24):6539-46. PubMed ID: 15556770
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  • 20. Synthesis and in vitro cytotoxic effect of 6-amino-substituted 11H- and 11Me-indolo[3,2-c]quinolines.
    Wang N, Świtalska M, Wu MY, Imai K, Ngoc TA, Pang CQ, Wang L, Wietrzyk J, Inokuchi T.
    Eur J Med Chem; 2014 May 06; 78():314-23. PubMed ID: 24686018
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