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Potential protease inhibitors based on a functionalized cyclic sulfamide scaffold.
J Comb Chem. 2004 Jul-Aug;6(4):556-63. doi: 10.1021/cc030047r.
J Comb Chem. 2004.
PMID: 15244417
Serendipitous discovery of an unexpected rearrangement leads to two new classes of potential protease inhibitors.
Zhong J, Lai Z, Groutas CS, Wong T, Gan X, Alliston KR, Eichhorn D, Hoidal JR, Groutas WC.
Zhong J, et al. Among authors: groutas cs.
Bioorg Med Chem. 2004 Dec 1;12(23):6249-54. doi: 10.1016/j.bmc.2004.08.044.
Bioorg Med Chem. 2004.
PMID: 15519167
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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.
Wong T, et al. Among authors: groutas cs.
Arch Biochem Biophys. 2005 Apr 1;436(1):1-7. doi: 10.1016/j.abb.2005.01.022.
Arch Biochem Biophys. 2005.
PMID: 15752703
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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.
Yang Q, et al. Among authors: groutas cs.
Arch Biochem Biophys. 2008 Jul 15;475(2):115-20. doi: 10.1016/j.abb.2008.04.020. Epub 2008 Apr 22.
Arch Biochem Biophys. 2008.
PMID: 18457652
Free PMC article.
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