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Journal Abstract Search

125 related items for PubMed ID: 16842999

  • 21. Azepanone-based inhibitors of human and rat cathepsin K.
    Marquis RW, Ru Y, LoCastro SM, Zeng J, Yamashita DS, Oh HJ, Erhard KF, Davis LD, Tomaszek TA, Tew D, Salyers K, Proksch J, Ward K, Smith B, Levy M, Cummings MD, Haltiwanger RC, Trescher G, Wang B, Hemling ME, Quinn CJ, Cheng HY, Lin F, Smith WW, Janson CA, Zhao B, McQueney MS, D'Alessio K, Lee CP, Marzulli A, Dodds RA, Blake S, Hwang SM, James IE, Gress CJ, Bradley BR, Lark MW, Gowen M, Veber DF.
    J Med Chem; 2001 Apr 26; 44(9):1380-95. PubMed ID: 11311061
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  • 22. Synthesis of peptide aldehyde derivatives as selective inhibitors of human cathepsin L and their inhibitory effect on bone resorption.
    Yasuma T, Oi S, Choh N, Nomura T, Furuyama N, Nishimura A, Fujisawa Y, Sohda T.
    J Med Chem; 1998 Oct 22; 41(22):4301-8. PubMed ID: 9784105
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  • 24. The slow-binding inhibition of cathepsin K by its propeptide.
    Billington CJ, Mason P, Magny MC, Mort JS.
    Biochem Biophys Res Commun; 2000 Oct 05; 276(3):924-9. PubMed ID: 11027570
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  • 25. Lysosomotropism of basic cathepsin K inhibitors contributes to increased cellular potencies against off-target cathepsins and reduced functional selectivity.
    Falgueyret JP, Desmarais S, Oballa R, Black WC, Cromlish W, Khougaz K, Lamontagne S, Massé F, Riendeau D, Toulmond S, Percival MD.
    J Med Chem; 2005 Dec 01; 48(24):7535-43. PubMed ID: 16302795
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  • 29. Design and synthesis of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 1.
    Liu H, Tully DC, Epple R, Bursulaya B, Li J, Harris JL, Williams JA, Russo R, Tumanut C, Roberts MJ, Alper PB, He Y, Karanewsky DS.
    Bioorg Med Chem Lett; 2005 Nov 15; 15(22):4979-84. PubMed ID: 16183279
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  • 34. Arylaminoethyl amides as novel non-covalent cathepsin K inhibitors.
    Altmann E, Renaud J, Green J, Farley D, Cutting B, Jahnke W.
    J Med Chem; 2002 Jun 06; 45(12):2352-4. PubMed ID: 12036343
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  • 35. Cathepsins X and B display distinct activity profiles that can be exploited for inhibitor design.
    Ménard R, Therrien C, Lachance P, Sulea T, Qo H, Alvarez-Hernandez AD, Roush WR.
    Biol Chem; 2001 May 06; 382(5):839-45. PubMed ID: 11517939
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  • 37. Beta-substituted cyclohexanecarboxamide: a nonpeptidic framework for the design of potent inhibitors of cathepsin K.
    Crane SN, Black WC, Palmer JT, Davis DE, Setti E, Robichaud J, Paquet J, Oballa RM, Bayly CI, McKay DJ, Somoza JR, Chauret N, Seto C, Scheigetz J, Wesolowski G, Massé F, Desmarais S, Ouellet M.
    J Med Chem; 2006 Feb 09; 49(3):1066-79. PubMed ID: 16451072
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  • 39. A structural screening approach to ketoamide-based inhibitors of cathepsin K.
    Barrett DG, Catalano JG, Deaton DN, Long ST, McFadyen RB, Miller AB, Miller LR, Wells-Knecht KJ, Wright LL.
    Bioorg Med Chem Lett; 2005 May 02; 15(9):2209-13. PubMed ID: 15837295
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