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PUBMED FOR HANDHELDS

Journal Abstract Search


209 related items for PubMed ID: 15081015

  • 1.
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  • 2. Synthesis of potent and highly selective nonguanidine azetidinone inhibitors of human tryptase.
    Bisacchi GS, Slusarchyk WA, Bolton SA, Hartl KS, Jacobs G, Mathur A, Meng W, Ogletree ML, Pi Z, Sutton JC, Treuner U, Zahler R, Zhao G, Seiler SM.
    Bioorg Med Chem Lett; 2004 May 03; 14(9):2227-31. PubMed ID: 15081014
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  • 3. Synthesis and SAR of 4-carboxy-2-azetidinone mechanism-based tryptase inhibitors.
    Sutton JC, Bolton SA, Hartl KS, Huang MH, Jacobs G, Meng W, Ogletree ML, Pi Z, Schumacher WA, Seiler SM, Slusarchyk WA, Treuner U, Zahler R, Zhao G, Bisacchi GS.
    Bioorg Med Chem Lett; 2002 Nov 04; 12(21):3229-33. PubMed ID: 12372540
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  • 4. Novel pyrazinone inhibitors of mast cell tryptase: synthesis and SAR evaluation.
    Hopkins C, Neuenschwander K, Scotese A, Jackson S, Nieduzak T, Pauls H, Liang G, Sides K, Cramer D, Cairns J, Maignan S, Mathieu M.
    Bioorg Med Chem Lett; 2004 Oct 04; 14(19):4819-23. PubMed ID: 15341931
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  • 8. Discovery of inhibitors of the channel-activating protease prostasin (CAP1/PRSS8) utilizing structure-based design.
    Tully DC, Vidal A, Chatterjee AK, Williams JA, Roberts MJ, Petrassi HM, Spraggon G, Bursulaya B, Pacoma R, Shipway A, Schumacher AM, Danahay H, Harris JL.
    Bioorg Med Chem Lett; 2008 Nov 15; 18(22):5895-9. PubMed ID: 18752942
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  • 14. Inhibition of human beta-tryptase by Bowman-Birk inhibitor derived peptides: creation of a new tri-functional inhibitor.
    Scarpi D, McBride JD, Leatherbarrow RJ.
    Bioorg Med Chem; 2004 Dec 01; 12(23):6045-52. PubMed ID: 15519150
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  • 15. Pyrrolidinyl pyridone and pyrazinone analogues as potent inhibitors of prolyl oligopeptidase (POP).
    Haffner CD, Diaz CJ, Miller AB, Reid RA, Madauss KP, Hassell A, Hanlon MH, Porter DJ, Becherer JD, Carter LH.
    Bioorg Med Chem Lett; 2008 Aug 01; 18(15):4360-3. PubMed ID: 18606544
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  • 16. Novel, potent, selective, and orally bioavailable human betaII-tryptase inhibitors.
    Sperandio D, Tai VW, Lohman J, Hirschbein B, Mendonca R, Lee CS, Spencer JR, Janc J, Nguyen M, Beltman J, Sprengeler P, Scheerens H, Lin T, Liu L, Gadre A, Kellogg A, Green MJ, McGrath ME.
    Bioorg Med Chem Lett; 2006 Aug 01; 16(15):4085-9. PubMed ID: 16725321
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  • 17. 1,2,5-Thiadiazolidin-3-one 1,1-dioxide-based heterocyclic sulfides are potent inhibitors of human tryptase.
    Wong T, Groutas CS, Mohan S, Lai Z, Alliston KR, Vu N, Schechter NM, Groutas WC.
    Arch Biochem Biophys; 2005 Apr 01; 436(1):1-7. PubMed ID: 15752703
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  • 18. Structure-based design of a novel series of azetidine inhibitors of the hepatitis C virus NS3/4A serine protease.
    Parsy C, Alexandre FR, Brandt G, Caillet C, Cappelle S, Chaves D, Convard T, Derock M, Gloux D, Griffon Y, Lallos L, Leroy F, Liuzzi M, Loi AG, Moulat L, Musiu C, Rahali H, Roques V, Seifer M, Standring D, Surleraux D.
    Bioorg Med Chem Lett; 2014 Sep 15; 24(18):4444-4449. PubMed ID: 25155387
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