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Literature summary for 3.4.21.109 extracted from

  • Paszti-Gere, E.; Barna, R.F.; Ujhelyi, G.; Steinmetzer, T.
    Interaction exists between matriptase inhibitors and intestinal epithelial cells (2016), J. Enzyme Inhib. Med. Chem., 31, 736-741 .
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
3-[(2S)-2-[[(2',4'-dimethoxybiphenyl-3-yl)sulfonyl]amino]-3-(4-[2-(methylcarbamoyl)aminoethyl]piperidin-1-yl)-3-oxopropyl]benzenecarboximidamide
-
Sus scrofa
3-[(2S)-3-[4-(2-aminoethyl)piperidin-1-yl]-2-[[(2',4'-dichlorobiphenyl-3-yl)sulfonyl]amino]-3-oxopropyl]benzenecarboximidamide
-
Sus scrofa
4-(2-aminoethyl)-benzosulphonylfluoride nonselective inhibitor Sus scrofa

Organism

Organism UniProt Comment Textmining
Sus scrofa F1S6D6
-
-

Source Tissue

Source Tissue Comment Organism Textmining
IPEC-J2 cell intestinal IPEC-J2 cell monolayer Sus scrofa
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
butyloxycarbonyl-Gln-Ala-Arg-7-amido-4-methylcoumarin + H2O
-
Sus scrofa ?
-
?

General Information

General Information Comment Organism
physiological function suppression of matriptase activity by inhibitors 3-[(2S)-2-[[(2',4'-dimethoxybiphenyl-3-yl)sulfonyl]amino]-3-(4-[2-(methylcarbamoyl)aminoethyl]piperidin-1-yl)-3-oxopropyl]benzenecarboximidamide and 3-[(2S)-3-[4-(2-aminoethyl)piperidin-1-yl]-2-[[(2',4'-dichlorobiphenyl-3-yl)sulfonyl]amino]-3-oxopropyl]benzenecarboximidamide leads to decreased transepithelial electrical resistance of the cell monolayer and to an enhanced transport of fluorescently labelled dextran Sus scrofa