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PUBMED FOR HANDHELDS

Journal Abstract Search


123 related items for PubMed ID: 7120060

  • 21. Synthesis and biological activity of stable and potent antitumor agents, aniline nitrogen mustards linked to 9-anilinoacridines via a urea linkage.
    Kapuriya N, Kapuriya K, Zhang X, Chou TC, Kakadiya R, Wu YT, Tsai TH, Chen YT, Lee TC, Shah A, Naliapara Y, Su TL.
    Bioorg Med Chem; 2008 May 15; 16(10):5413-23. PubMed ID: 18450456
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  • 25. Synthesis and structure-activity relationships of pre-activated analogs of cyclophosphamide (NSC-26271).
    Montgomery JA, Struck RF.
    Cancer Treat Rep; 1976 Apr 15; 60(4):381-93. PubMed ID: 945126
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  • 26. Steroidal esters of the aromatic nitrogen mustard 2-[4-N,N-bis(2-chloroethyl)amino-phenyl]butanoic acid (2-PHE-BU): synthesis and in-vivo biological evaluation.
    Papaconstantinou IC, Fousteris MA, Koutsourea AI, Pairas GN, Papageorgiou AD, Nikolaropoulos SS.
    Anticancer Drugs; 2013 Jan 15; 24(1):52-65. PubMed ID: 23187313
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  • 29. Preparation of 4-(p-(bis(2-chloroethyl)amino)phenyl)butyramides as potential antitumor agents. I.
    Billman JH, Roehrig GR.
    J Pharm Sci; 1974 Sep 15; 63(9):1487-9. PubMed ID: 4427280
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  • 32. In the search for new anticancer drugs. XXIV: Synthesis and anticancer activity of amino acids and dipeptides containing the 2-chloroethyl- and [N'-(2-chloroethyl)-N'-nitroso]-aminocarbonyl groups.
    Sosnovsky G, Prakash I, Rao NU.
    J Pharm Sci; 1993 Jan 15; 82(1):1-10. PubMed ID: 8429483
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  • 33. Antitumor activity and bone marrow toxicity of aminoglucose mustard anticancer agents in mice.
    Cantrell JE, Green D, Schein PS.
    Cancer Res; 1986 May 15; 46(5):2340-3. PubMed ID: 2938728
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  • 34. Conjugated system of homo-aza-steroidal esters in cancer chemotherapy.
    Catsoulacos P, Catsoulacos D.
    Anticancer Res; 1994 May 15; 14(6B):2525-8. PubMed ID: 7872677
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  • 35. [N-quaternary derivatives of tilorone].
    Schulze W, Letsch G, Gutsche W, Wohlrabe K, Tresselt D.
    Pharmazie; 1984 May 15; 39(5):320-2. PubMed ID: 6473490
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  • 36. (2-Chloroethyl)nitrosourea congeners of amino acid amides.
    Suami T, Kato T, Takino H, Hisamatsu T.
    J Med Chem; 1982 Jul 15; 25(7):829-32. PubMed ID: 7108898
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  • 37. Synthesis and evaluation of 1-acyl-1,2-bis(methylsulfonyl)-2-(2- chloroethyl)hydrazines as antineoplastic agents.
    Shyam K, Penketh PG, Divo AA, Loomis RH, Rose WC, Sartorelli AC.
    J Med Chem; 1993 Nov 12; 36(23):3496-502. PubMed ID: 8246218
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  • 38. Research on compounds with antiblastic activity. XL. Synthesis of 3-p-(2',5'-dimethoxy-4'-(N,N-bis-( -chloroethyl)-amino)benzylideneamino)phenyl-2-oxazolidinone (GEA 29 ; BAY a 5850) and its analogues.
    Artico M, De Martino G, Giuliano R.
    Farmaco Sci; 1971 Sep 12; 26(9):771-83. PubMed ID: 5157545
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  • 39. Selective cytotoxicity of a system L specific amino acid nitrogen mustard.
    Haines DR, Fuller RW, Ahmad S, Vistica DT, Marquez VE.
    J Med Chem; 1987 Mar 12; 30(3):542-7. PubMed ID: 3820226
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  • 40. Hypoxia-selective antitumor agents. 9. Structure-activity relationships for hypoxia-selective cytotoxicity among analogues of 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide.
    Palmer BD, Wilson WR, Atwell GJ, Schultz D, Xu XZ, Denny WA.
    J Med Chem; 1994 Jul 08; 37(14):2175-84. PubMed ID: 8035424
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