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PUBMED FOR HANDHELDS

Journal Abstract Search


345 related items for PubMed ID: 16644213

  • 1. Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-acyl aromatic alpha-amino acids.
    Stranix BR, Lavallée JF, Sévigny G, Yelle J, Perron V, LeBerre N, Herbart D, Wu JJ.
    Bioorg Med Chem Lett; 2006 Jul 01; 16(13):3459-62. PubMed ID: 16644213
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  • 2. Lysine sulfonamides as novel HIV-protease inhibitors: Nepsilon-disubstituted ureas.
    Stranix BR, Sauvé G, Bouzide A, Coté A, Sévigny G, Yelle J, Perron V.
    Bioorg Med Chem Lett; 2004 Aug 02; 14(15):3971-4. PubMed ID: 15225709
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  • 4. Synthesis, antiviral activity, and pharmacokinetic evaluation of P3 pyridylmethyl analogs of oximinoarylsulfonyl HIV-1 protease inhibitors.
    Randolph JT, Huang PP, Flosi WJ, DeGoey D, Klein LL, Yeung CM, Flentge C, Sun M, Zhao C, Dekhtyar T, Mo H, Colletti L, Kati W, Marsh KC, Molla A, Kempf DJ.
    Bioorg Med Chem; 2006 Jun 15; 14(12):4035-46. PubMed ID: 16504523
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  • 6. Lysine sulfonamides as novel HIV-protease inhibitors: optimization of the Nepsilon-acyl-phenyl spacer.
    Stranix BR, Sauvé G, Bouzide A, Coté A, Sévigny G, Yelle J.
    Bioorg Med Chem Lett; 2003 Dec 15; 13(24):4289-92. PubMed ID: 14643311
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  • 8. Oximinoarylsulfonamides as potent HIV protease inhibitors.
    Yeung CM, Klein LL, Flentge CA, Randolph JT, Zhao C, Sun M, Dekhtyar T, Stoll VS, Kempf DJ.
    Bioorg Med Chem Lett; 2005 May 02; 15(9):2275-8. PubMed ID: 15837308
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  • 12. Novel inhibitors of HIV protease: design, synthesis and biological evaluation of picomolar inhibitors containing cyclic P1/P2 scaffolds.
    Spaltenstein A, Almond MR, Bock WJ, Cleary DG, Furfine ES, Hazen RJ, Kazmierski WM, Salituro FG, Tung RD, Wright LL.
    Bioorg Med Chem Lett; 2000 Jun 05; 10(11):1159-62. PubMed ID: 10866371
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  • 14. Lysine derivatives as potent HIV protease inhibitors. Discovery, synthesis and structure-activity relationship studies.
    Bouzide A, Sauvé G, Yelle J.
    Bioorg Med Chem Lett; 2005 Mar 01; 15(5):1509-13. PubMed ID: 15713418
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  • 15. Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: the discovery of GW0385.
    Miller JF, Andrews CW, Brieger M, Furfine ES, Hale MR, Hanlon MH, Hazen RJ, Kaldor I, McLean EW, Reynolds D, Sammond DM, Spaltenstein A, Tung R, Turner EM, Xu RX, Sherrill RG.
    Bioorg Med Chem Lett; 2006 Apr 01; 16(7):1788-94. PubMed ID: 16458505
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  • 16. Synthesis and antiviral activity of P1' arylsulfonamide azacyclic urea HIV protease inhibitors.
    Huang PP, Randolph JT, Klein LL, Vasavanonda S, Dekhtyar T, Stoll VS, Kempf DJ.
    Bioorg Med Chem Lett; 2004 Aug 02; 14(15):4075-8. PubMed ID: 15225729
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  • 18. Cyclic HIV-1 protease inhibitors derived from mannitol: synthesis, inhibitory potencies, and computational predictions of binding affinities.
    Hultén J, Bonham NM, Nillroth U, Hansson T, Zuccarello G, Bouzide A, Aqvist J, Classon B, Danielson UH, Karlén A, Kvarnström I, Samuelsson B, Hallberg A.
    J Med Chem; 1997 Mar 14; 40(6):885-97. PubMed ID: 9083477
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