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Journal Abstract Search

205 related items for PubMed ID: 19945869

  • 1. Pyrrole derivatives as potent inhibitors of lymphocyte-specific kinase: Structure, synthesis, and SAR.
    Takayama T, Umemiya H, Amada H, Yabuuchi T, Shiozawa F, Katakai H, Takaoka A, Yamaguchi A, Endo M, Sato M.
    Bioorg Med Chem Lett; 2010 Jan 01; 20(1):108-11. PubMed ID: 19945869
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  • 6. Discovery of 2-amino-6-carboxamidobenzothiazoles as potent Lck inhibitors.
    Huang S, Liu Z, Tian SS, Sandberg M, Spalding TA, Romeo R, Iskandar M, Wang Z, Karanewsky D, He Y.
    Bioorg Med Chem Lett; 2008 Apr 01; 18(7):2324-8. PubMed ID: 18353642
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  • 14. Discovery of 4-amino-5,6-biaryl-furo[2,3-d]pyrimidines as inhibitors of Lck: development of an expedient and divergent synthetic route and preliminary SAR.
    DiMauro EF, Newcomb J, Nunes JJ, Bemis JE, Boucher C, Buchanan JL, Buckner WH, Cheng A, Faust T, Hsieh F, Huang X, Lee JH, Marshall TL, Martin MW, McGowan DC, Schneider S, Turci SM, White RD, Zhu X.
    Bioorg Med Chem Lett; 2007 Apr 15; 17(8):2305-9. PubMed ID: 17280833
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  • 15. Discovery of pyrimidine benzimidazoles as Src-family selective Lck inhibitors. Part II.
    Zhang G, Ren P, Gray NS, Sim T, Wang X, Liu Y, Che J, Dong W, Tian SS, Sandberg ML, Spalding TA, Romeo R, Iskandar M, Wang Z, Seidel HM, Karanewsky DS, He Y.
    Bioorg Med Chem Lett; 2009 Dec 01; 19(23):6691-5. PubMed ID: 19854052
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