Protease Inhibitors

Biochem/physiol Actions (+)-JQ-1 carboxylic acid is a potent BET (bromodomain and extra terminal domain) inhibitor. (+)-JQ-1 carboxylic acid could serve as precursor to synthesize PROTACs and other conjugates.

Biochem/physiol Actions (+)-JQ-1 carboxylic acid is a potent BET (bromodomain and extra terminal domain) inhibitor. (+)-JQ-1 carboxylic acid could serve as precursor to synthesize PROTACs and other conjugates.

Product Application：cis-3-Benzoylcyclohexane-1-carboxylic Acid as aspartic protease inhibitors.

Product Application：cis-3-Benzoylcyclohexane-1-carboxylic Acid as aspartic protease inhibitors.

Product Application：cis-3-Benzoylcyclohexane-1-carboxylic Acid as aspartic protease inhibitors.

(1 S ,2 R )-(-)- cis -1-Amino-2-indanol is a main constituent of indinavir, a potent HIV (human immunodeficiency virus) protease inhibitor. Application 1 S ,2 R )-(-)- cis -1-Amino-2-indanol may be used to prepare: (-)-1,2,5,6-Tetrahydropyridine by

A potent, reversible, and cell permeable proteasome inhibitor a more effective inhibitor of chymotrypsin-like, trypsin-like, and peptidylglutamyl peptide hydrolyzing proteasome activities compared to (S)-MG132 (IC₅₀s = 0.22 versus 0.

A potent, reversible, and cell permeable proteasome inhibitor a more effective inhibitor of chymotrypsin-like, trypsin-like, and peptidylglutamyl peptide hydrolyzing proteasome activities compared to (S)-MG132 (IC₅₀s = 0.22 versus 0.

A potent, reversible, and cell permeable proteasome inhibitor a more effective inhibitor of chymotrypsin-like, trypsin-like, and peptidylglutamyl peptide hydrolyzing proteasome activities compared to (S)-MG132 (IC₅₀s = 0.22 versus 0.

InformationCPD77 (MUN91789) is a potent inhibitor of SARS-​CoV-​2 main protease.

InformationCPD77 (MUN91789) is a potent inhibitor of SARS-​CoV-​2 main protease.

InformationCPD77 (MUN91789) is a potent inhibitor of SARS-​CoV-​2 main protease.