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Literature summary for 3.4.21.37 extracted from

  • Wei, L.; Lai, Z.; Gan, X.; Alliston, K.R.; Zhong, J.; Epp, J.B.; Tu, J.; Perera, A.B.; Van Stipdonk, M.; Groutas, W.C.
    Mechanism-based inactivation of human leukocyte elastase via an enzyme-induced sulfonamide fragmentation process (2004), Arch. Biochem. Biophys., 429, 60-70.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
(R)-3-phenyl-2-(1,1,3-trioxo-1,3-dihydro-1lambda6-1,2-benzisothiazol-2-yl-methanesulfonylamino)-propionic acid methyl ester
-
Homo sapiens
(S)-3-phenyl-2-(1,1,3-trioxo-1,3-dihydro-1lambda6-1,2-benzisothiazol-2-yl-methanesulfonylamino)-propionic acid methyl ester
-
Homo sapiens
additional information shows no activity as inhibitor Homo sapiens
N-(2,2-diphenyl-ethyl)-1-(1,1,3-trioxo-1,3-dihydro-1lambda6-1,2-benzisothiazol-2-yl)-methanesulfonamide
-
Homo sapiens
N-benzyl-1-(1,1,3-trioxo-1,3-dihydro-1lambda6-1,2-benzisothiazol-2-yl)-methanesulfonamide
-
Homo sapiens
N-phenethyl-1-(1,1,3-trioxo-1,3-dihydro-1lambda6-1,2-benzisothiazol-2-yl)-methanesulfonamide
-
Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining