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PUBMED FOR HANDHELDS

Journal Abstract Search


130 related items for PubMed ID: 16203141

  • 21. Novel lopinavir analogues incorporating heterocyclic replacements of six-member cyclic urea--synthesis and structure-activity relationships.
    Sham HL, Betebenner DA, Rosenbrook W, Herrin T, Saldivar A, Vasavanonda S, Plattner JJ, Norbeck DW.
    Bioorg Med Chem Lett; 2004 May 17; 14(10):2643-5. PubMed ID: 15109669
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  • 22. Predictors of virologic response to ritonavir-boosted protease inhibitors.
    Marcelin AG, Flandre P, Peytavin G, Calvez V.
    AIDS Rev; 2005 May 17; 7(4):225-32. PubMed ID: 16425962
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  • 23. Structure-activity relationships of novel HIV-1 protease inhibitors containing the 3-amino-2-chlorobenzoyl-allophenylnorstatine structure.
    Mimoto T, Nojima S, Terashima K, Takaku H, Shintani M, Hayashi H.
    Bioorg Med Chem; 2008 Feb 01; 16(3):1299-308. PubMed ID: 17981045
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  • 24. Synthesis and antiviral property of allophenylnorstatine-based HIV protease inhibitors incorporating D-cysteine derivatives as P2/P3 moieties.
    Ami E, Nakahara K, Sato A, Nguyen JT, Hidaka K, Hamada Y, Nakatani S, Kimura T, Hayashi Y, Kiso Y.
    Bioorg Med Chem Lett; 2007 Aug 01; 17(15):4213-7. PubMed ID: 17537628
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  • 26. Indium-mediated atom-transfer and reductive radical cyclizations of iodoalkynes: synthesis and biological evaluation of HIV-protease inhibitors.
    Yanada R, Koh Y, Nishimori N, Matsumura A, Obika S, Mitsuya H, Fujii N, Takemoto Y.
    J Org Chem; 2004 Apr 02; 69(7):2417-22. PubMed ID: 15049639
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  • 30. Nonsymmetrically substituted cyclic urea HIV protease inhibitors.
    Wilkerson WW, Dax S, Cheatham WW.
    J Med Chem; 1997 Dec 05; 40(25):4079-88. PubMed ID: 9406598
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  • 32. Optimization and computational evaluation of a series of potential active site inhibitors of the V82F/I84V drug-resistant mutant of HIV-1 protease: an application of the relaxed complex method of structure-based drug design.
    Perryman AL, Lin JH, Andrew McCammon J.
    Chem Biol Drug Des; 2006 May 05; 67(5):336-45. PubMed ID: 16784458
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  • 34. Cyclic HIV protease inhibitors: design and synthesis of orally bioavailable, pyrazole P2/P2' cyclic ureas with improved potency.
    Han Q, Chang CH, Li R, Ru Y, Jadhav PK, Lam PY.
    J Med Chem; 1998 Jun 04; 41(12):2019-28. PubMed ID: 9622543
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  • 36. Preliminary safety and efficacy data of brecanavir, a novel HIV-1 protease inhibitor: 24 week data from study HPR10006.
    Lalezari JP, Ward DJ, Tomkins SA, Garges HP.
    J Antimicrob Chemother; 2007 Jul 04; 60(1):170-4. PubMed ID: 17491001
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  • 37. PL-100, a novel HIV-1 protease inhibitor displaying a high genetic barrier to resistance: an in vitro selection study.
    Dandache S, Coburn CA, Oliveira M, Allison TJ, Holloway MK, Wu JJ, Stranix BR, Panchal C, Wainberg MA, Vacca JP.
    J Med Virol; 2008 Dec 04; 80(12):2053-63. PubMed ID: 19040279
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