1,2,5-Thiadiazolidin-3-one 1,1-dioxide-based heterocyclic sulfides are potent inhibitors of human tryptase

Archives of Biochemistry and Biophysics

Volumn 436, Issue 1, 2005, Pages 1-7

  Wong, Tzutshin ^a   Groutas, Christopher S ^a   Mohan, Swathi ^a   Lai, Zhong ^a   Alliston, Kevin R ^a   Vu, Nga ^a   Schechter, Norman M ^b   Groutas, William C ^a  

^a WICHITA STATE UNIVERSITY   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Mechanism based inhibitors; Tryptase

Indexed keywords

ELASTASE; ENZYME INHIBITOR; PAPAIN; PROTEINASE; SERINE PROTEINASE; THIADIAZOLE DERIVATIVE; TRYPSIN; TRYPTASE INHIBITOR;

ARTICLE; CONTROLLED STUDY; COW; DRUG DESIGN; DRUG EFFECT; DRUG POTENCY; DRUG SYNTHESIS; ENZYME INHIBITION; HUMAN; MAST CELL; NONHUMAN; PRIORITY JOURNAL;

EID: 14744287476     PISSN: 00039861     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.abb.2005.01.022     Document Type: Article

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