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Journal Abstract Search

177 related items for PubMed ID: 8367461

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  • 3. Cyclotheonamide derivatives: synthesis and thrombin inhibition. Exploration of specific structure-function issues.
    Maryanoff BE, Zhang HC, Greco MN, Glover KA, Kauffman JA, Andrade-Gordon P.
    Bioorg Med Chem; 1995 Aug; 3(8):1025-38. PubMed ID: 7582977
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  • 4. Inhibition of thrombin and other trypsin-like serine proteinases by cyclotheonamide A.
    Lewis SD, Ng AS, Baldwin JJ, Fusetani N, Naylor AM, Shafer JA.
    Thromb Res; 1993 Apr 15; 70(2):173-90. PubMed ID: 8322286
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  • 6. A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site.
    Katz BA, Elrod K, Luong C, Rice MJ, Mackman RL, Sprengeler PA, Spencer J, Hataye J, Janc J, Link J, Litvak J, Rai R, Rice K, Sideris S, Verner E, Young W.
    J Mol Biol; 2001 Apr 13; 307(5):1451-86. PubMed ID: 11292354
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  • 9. Crystallographic structure of a peptidyl keto acid inhibitor and human alpha-thrombin.
    Håkansson K, Tulinsky A, Abelman MM, Miller TA, Vlasuk GP, Bergum PW, Lim-Wilby MS, Brunck TK.
    Bioorg Med Chem; 1995 Aug 13; 3(8):1009-17. PubMed ID: 7582975
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  • 11. Think twice: understanding the high potency of bis(phenyl)methane inhibitors of thrombin.
    Baum B, Muley L, Heine A, Smolinski M, Hangauer D, Klebe G.
    J Mol Biol; 2009 Aug 21; 391(3):552-64. PubMed ID: 19520086
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  • 12. Molecular design and characterization of an alpha-thrombin inhibitor containing a novel P1 moiety.
    Malikayil JA, Burkhart JP, Schreuder HA, Broersma RJ, Tardif C, Kutcher LW, Mehdi S, Schatzman GL, Neises B, Peet NP.
    Biochemistry; 1997 Feb 04; 36(5):1034-40. PubMed ID: 9033393
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  • 13. Potent, multi-target serine protease inhibition achieved by a simplified β-sheet motif.
    Chen X, Riley BT, de Veer SJ, Hoke DE, Van Haeften J, Leahy D, Swedberg JE, Brattsand M, Hartfield PJ, Buckle AM, Harris JM.
    PLoS One; 2019 Feb 04; 14(1):e0210842. PubMed ID: 30668585
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  • 14. Cyclotheonamides E2 and E3, new potent serine protease inhibitors from the marine sponge of the genus Theonella.
    Nakao Y, Oku N, Matsunaga S, Fusetani N.
    J Nat Prod; 1998 May 04; 61(5):667-70. PubMed ID: 9599274
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  • 17. Crystal structure of two new bifunctional nonsubstrate type thrombin inhibitors complexed with human alpha-thrombin.
    Féthière J, Tsuda Y, Coulombe R, Konishi Y, Cygler M.
    Protein Sci; 1996 Jun 04; 5(6):1174-83. PubMed ID: 8762149
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  • 18. The crystal structures of human alpha-thrombin complexed with active site-directed diamino benzo[b]thiophene derivatives: a binding mode for a structurally novel class of inhibitors.
    Chirgadze NY, Sall DJ, Briggs SL, Clawson DK, Zhang M, Smith GF, Schevitz RW.
    Protein Sci; 2000 Jan 04; 9(1):29-36. PubMed ID: 10739244
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  • 19. Crystallographic determination of the structures of human alpha-thrombin complexed with BMS-186282 and BMS-189090.
    Malley MF, Tabernero L, Chang CY, Ohringer SL, Roberts DG, Das J, Sack JS.
    Protein Sci; 1996 Feb 04; 5(2):221-8. PubMed ID: 8745399
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  • 20. Crystal structure of the complex of human alpha-thrombin and nonhydrolyzable bifunctional inhibitors, hirutonin-2 and hirutonin-6.
    Zdanov A, Wu S, DiMaio J, Konishi Y, Li Y, Wu X, Edwards BF, Martin PD, Cygler M.
    Proteins; 1993 Nov 04; 17(3):252-65. PubMed ID: 8272424
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