Protease Inhibitors

Anti-XPNPEP3 X-prolyl aminopeptidase (aminopeptidase P) 3, p

Potent reversible inhibitor of serine/cysteine proteases and some trypsin-like proteases. Inhibits papain, trypsin and trypsin-like serine proteases as well as cathepsin A, B and D.

Potent reversible inhibitor of serine/cysteine proteases and some trypsin-like proteases. Inhibits papain, trypsin and trypsin-like serine proteases as well as cathepsin A, B and D.

Antipain is a serine and cysteine reversible protease inhibitor. It inhibits papain and trypsin.

Chemical structure: peptide Biochem/physiol Actions Reversible inhibitor of serine/cysteine proteases and some trypsin-like serine proteases. Its action resembles leupeptin however, its plasmin inhibition is less and its cathepsin A inhibition is

Chemical structure: peptide Biochem/physiol Actions Reversible inhibitor of serine/cysteine proteases and some trypsin-like serine proteases. Its action resembles leupeptin however, its plasmin inhibition is less and its cathepsin A inhibition is

Application APhos Pd G4 is a powerful ligand for classic cross-coupling reactions combined with the Buchwald Fourth Generation Palladacycle. Bench stable, soluble in most organic solvents.

Application APhos Pd G4 is a powerful ligand for classic cross-coupling reactions combined with the Buchwald Fourth Generation Palladacycle. Bench stable, soluble in most organic solvents.

A competitive and reversible inhibitor of esterase and protease activity. Forms a tight complex with and blocks the active site of target enzymes.

A competitive and reversible inhibitor of esterase and protease activity. Forms a tight complex with and blocks the active site of target enzymes.

General description A competitive and reversible inhibitor of esterase and protease activity. Forms a tight complex with and blocks the active site of target enzymes.

Application Aprotinin is largely used as an inhibitor of trypsin. Gel filtration molecular weight marker Biochem/physiol Actions Aprotinin is a competitive serine protease inhibitor that forms stable complexes with and blocks the active sites of