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Journal Abstract Search

182 related items for PubMed ID: 19394830

  • 1.
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  • 2. Inactivation of human neutrophil elastase by 1,2,5-thiadiazolidin-3-one 1,1 dioxide-based sulfonamides.
    Li Y, Yang Q, Dou D, Alliston KR, Groutas WC.
    Bioorg Med Chem; 2008 Jan 15; 16(2):692-8. PubMed ID: 17976994
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  • 4. 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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  • 6. Inhibition of serine proteases by functionalized sulfonamides coupled to the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold.
    Groutas WC, He S, Kuang R, Ruan S, Tu J, Chan HK.
    Bioorg Med Chem; 2001 Jun 01; 9(6):1543-8. PubMed ID: 11408173
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  • 7. Effects of structure on inhibitory activity in a series of mechanism-based inhibitors of human neutrophil elastase.
    Dou D, He G, Kuang R, Fu Q, Venkataraman R, Groutas WC.
    Bioorg Med Chem; 2010 Sep 15; 18(18):6646-50. PubMed ID: 20728366
    [Abstract] [Full Text] [Related]

  • 8. Potent inhibition of serine proteases by heterocyclic sulfide derivatives of 1,2,5-thiadiazolidin-3-one 1,1 dioxide.
    He S, Kuang R, Venkataraman R, Tu J, Truong TM, Chan HK, Groutas WC.
    Bioorg Med Chem; 2000 Jul 15; 8(7):1713-7. PubMed ID: 10976518
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  • 10. The serpin MNEI inhibits elastase-like and chymotrypsin-like serine proteases through efficient reactions at two active sites.
    Cooley J, Takayama TK, Shapiro SD, Schechter NM, Remold-O'Donnell E.
    Biochemistry; 2001 Dec 25; 40(51):15762-70. PubMed ID: 11747453
    [Abstract] [Full Text] [Related]

  • 11. 1,2,5-Thiadiazolidin-3-one 1,1 dioxide: a powerful scaffold for probing the S' subsites of (chymo)trypsin-like serine proteases.
    Groutas WC, Epp JB, Kuang R, Ruan S, Chong LS, Venkataraman R, Tu J, He S, Yu H, Fu Q, Li YH, Truong TM, Vu NT.
    Arch Biochem Biophys; 2001 Jan 01; 385(1):162-9. PubMed ID: 11361013
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  • 14. Inhibition of serine proteases by a new class of cyclosulfamide-based carbamylating agents.
    Yang Q, Li Y, Dou D, Gan X, Mohan S, Groutas CS, Stevenson LE, Lai Z, Alliston KR, Zhong J, Williams TD, Groutas WC.
    Arch Biochem Biophys; 2008 Jul 15; 475(2):115-20. PubMed ID: 18457652
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  • 16. Phosphonic pseudopeptides as human neutrophil elastase inhibitors--a combinatorial approach.
    Sieńczyk M, Podgórski D, Błażejewska A, Kulbacka J, Saczko J, Oleksyszyn J.
    Bioorg Med Chem; 2011 Feb 01; 19(3):1277-84. PubMed ID: 21216608
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  • 18. Use of the 1,2,5-thiadiazolidin-3-one 1,1 dioxide and isothiazolidin-3-one 1,1 dioxide scaffolds in the design of potent inhibitors of serine proteinases.
    Kuang R, Venkataraman R, Ruan S, Groutas WC.
    Bioorg Med Chem Lett; 1998 Mar 03; 8(5):539-44. PubMed ID: 9871614
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  • 20. Design, synthesis, and in vitro evaluation of inhibitors of human leukocyte elastase based on a functionalized cyclic sulfamide scaffold.
    Zhong J, Gan X, Alliston KR, Groutas WC.
    Bioorg Med Chem; 2004 Feb 01; 12(3):589-93. PubMed ID: 14738969
    [Abstract] [Full Text] [Related]

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