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Journal Abstract Search

1344 related items for PubMed ID: 9568100

  • 1. The primary in vitro anticancer activity of "half-mustard type" phenothiazines in NCI's revised anticancer screening paradigm.
    Wuonola MA, Palfreyman MG, Motohashi N, Kawase M, Gabay S, Gupta RR, Molnár J.
    Anticancer Res; 1998; 18(1A):337-48. PubMed ID: 9568100
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  • 2. The primary in vitro antitumor screening of "half-mustard type" phenothiazines.
    Wuonola MA, Palfreyman MG, Motohashi N, Kawase M, Gabay S, Nacsa J, Molnár J.
    Anticancer Res; 1997; 17(5A):3409-23. PubMed ID: 9413180
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  • 3. The in vitro antitumor assay of "half-mustard type" phenothiazines in screens of AIDS-related leukemia and lymphomas.
    Wuonola MA, Palfreyman MG, Motohashi N, Kawase M, Gabay S, Molnár J.
    Anticancer Res; 1997; 17(5A):3425-9. PubMed ID: 9413181
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  • 4. Chemical structure and tumor type specificity of "half-mustard type" phenothiazines.
    Motohashi N, Kurihara T, Sakagami H, Szabo D, Csuri K, Molnár J.
    Anticancer Res; 1999; 19(3A):1859-64. PubMed ID: 10470128
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  • 5. Antitumor activity of phenothiazine-related compounds.
    Nagy S, Argyelan G, Molnár J, Kawase M, Motohashi N.
    Anticancer Res; 1996; 16(4A):1915-8. PubMed ID: 8712720
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  • 6. The cytotoxicity of methyl protoneogracillin (NSC-698793) and gracillin (NSC-698787), two steroidal saponins from the rhizomes of Dioscorea collettii var. hypoglauca, against human cancer cells in vitro.
    Hu K, Yao X.
    Phytother Res; 2003 Jun; 17(6):620-6. PubMed ID: 12820229
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  • 7. The cytotoxicity of methyl protoneodioscin (NSC-698791) against human cancer cell lines in vitro.
    Hu K, Yao XS.
    Anticancer Res; 2002 Jun; 22(2A):1001-5. PubMed ID: 12014616
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  • 10. Protodioscin (NSC-698 796): its spectrum of cytotoxicity against sixty human cancer cell lines in an anticancer drug screen panel.
    Hu K, Yao X.
    Planta Med; 2002 Apr; 68(4):297-301. PubMed ID: 11988850
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  • 11. Molecular modes of action of cephalotaxine and homoharringtonine from the coniferous tree Cephalotaxus hainanensis in human tumor cell lines.
    Efferth T, Sauerbrey A, Halatsch ME, Ross DD, Gebhart E.
    Naunyn Schmiedebergs Arch Pharmacol; 2003 Jan; 367(1):56-67. PubMed ID: 12616342
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  • 18. Antitumor agents. 178. Synthesis and biological evaluation of substituted 2-aryl-1,8-naphthyridin-4(1H)-ones as antitumor agents that inhibit tubulin polymerization.
    Chen K, Kuo SC, Hsieh MC, Mauger A, Lin CM, Hamel E, Lee KH.
    J Med Chem; 1997 Sep 12; 40(19):3049-56. PubMed ID: 9301667
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