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Journal Abstract Search

261 related items for PubMed ID: 20184370

  • 21. Hybrid inhibitors of phosphatidylinositol 3-kinase (PI3K) and the mammalian target of rapamycin (mTOR): design, synthesis, and superior antitumor activity of novel wortmannin-rapamycin conjugates.
    Ayral-Kaloustian S, Gu J, Lucas J, Cinque M, Gaydos C, Zask A, Chaudhary I, Wang J, Di L, Young M, Ruppen M, Mansour TS, Gibbons JJ, Yu K.
    J Med Chem; 2010 Jan 14; 53(1):452-9. PubMed ID: 19928864
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  • 22. Synthesis and cytotoxicity of novel indirubin-5-carboxamides.
    Cheng X, Rasqué P, Vatter S, Merz KH, Eisenbrand G.
    Bioorg Med Chem; 2010 Jun 15; 18(12):4509-15. PubMed ID: 20488718
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  • 23. Synthesis and antitumour activity of new muricatacin and goniofufurone analogues.
    Popsavin V, Srećo B, Krstić I, Popsavin M, Kojić V, Bogdanović G.
    Eur J Med Chem; 2006 Oct 15; 41(10):1217-22. PubMed ID: 16891043
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  • 24. 4-Anilino-7-pyridyl-3-quinolinecarbonitriles as Src kinase inhibitors.
    Zhang N, Wu B, Boschelli DH, Golas JM, Boschelli F.
    Bioorg Med Chem Lett; 2009 Sep 01; 19(17):5071-4. PubMed ID: 19632113
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  • 26. ATP non-competitive IGF-1 receptor kinase inhibitors as lead anti-neoplastic and anti-papilloma agents.
    Steiner L, Blum G, Friedmann Y, Levitzki A.
    Eur J Pharmacol; 2007 May 07; 562(1-2):1-11. PubMed ID: 17376430
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  • 27. Synthesis and biological evaluation of selective and potent cyclin-dependent kinase inhibitors.
    N'gompaza-Diarra J, Bettayeb K, Gresh N, Meijer L, Oumata N.
    Eur J Med Chem; 2012 Oct 07; 56():210-6. PubMed ID: 22982525
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  • 31. Evaluation of a series of naphthamides as potent, orally active vascular endothelial growth factor receptor-2 tyrosine kinase inhibitors.
    Weiss MM, Harmange JC, Polverino AJ, Bauer D, Berry L, Berry V, Borg G, Bready J, Chen D, Choquette D, Coxon A, DeMelfi T, Doerr N, Estrada J, Flynn J, Graceffa RF, Harriman SP, Kaufman S, La DS, Long A, Neervannan S, Patel VF, Potashman M, Regal K, Roveto PM, Schrag ML, Starnes C, Tasker A, Teffera Y, Whittington DA, Zanon R.
    J Med Chem; 2008 Mar 27; 51(6):1668-80. PubMed ID: 18324759
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  • 36. Synthesis and biological activities of 4-substituted pyrrolo[2,3-a]carbazole Pim kinase inhibitors.
    Giraud F, Akué-Gédu R, Nauton L, Candelon N, Debiton E, Théry V, Anizon F, Moreau P.
    Eur J Med Chem; 2012 Oct 27; 56():225-36. PubMed ID: 22982527
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  • 38. Omega-alkoxy analogues of SAHA (vorinostat) as inhibitors of HDAC: a study of chain-length and stereochemical dependence.
    Hanessian S, Auzzas L, Giannini G, Marzi M, Cabri W, Barbarino M, Vesci L, Pisano C.
    Bioorg Med Chem Lett; 2007 Nov 15; 17(22):6261-5. PubMed ID: 17892933
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  • 39. Design and synthesis of orally bioavailable benzimidazoles as Raf kinase inhibitors.
    Ramurthy S, Subramanian S, Aikawa M, Amiri P, Costales A, Dove J, Fong S, Jansen JM, Levine B, Ma S, McBride CM, Michaelian J, Pick T, Poon DJ, Girish S, Shafer CM, Stuart D, Sung L, Renhowe PA.
    J Med Chem; 2008 Nov 27; 51(22):7049-52. PubMed ID: 18942827
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