Protease Inhibitors

A reversible inhibitor of serine proteases such as trypsin (Ki = 0.06 pM), chymotrypsin (Ki = 9.

Immunogen 17 amino amino terminus of human ARC. Application Used as a blocking peptide in immunoblotting applications.

ARD-61 is a highly potent, effective and specific PROTAC androgen receptor (AR) degrader. ARD-61 potently and effectively induces AR and progesterone receptors (PR) degradation in AR+ cancer cell lines. ARD-61 induces apoptosis and effectively

An aminopeptidase B inhibitor that is commonly used to characterize novel proteases.

Asunaprevir (BMS-650032) is a potent hepatitis C virus (HCV) NS3 protease inhibitor.An inhibitor of the viral enzyme serine protease HCV NS3.

Asunaprevir (BMS-650032) is a potent hepatitis C virus (HCV) NS3 protease inhibitor.An inhibitor of the viral enzyme serine protease HCV NS3.

Asunaprevir (BMS-650032) is a potent hepatitis C virus (HCV) NS3 protease inhibitor.An inhibitor of the viral enzyme serine protease HCV NS3.

Asunaprevir (BMS-650032) is a potent hepatitis C virus (HCV) NS3 protease inhibitor.An inhibitor of the viral enzyme serine protease HCV NS3.

Asunaprevir (BMS-650032) is a potent hepatitis C virus (HCV) NS3 protease inhibitor.An inhibitor of the viral enzyme serine protease HCV NS3.

Asunaprevir (BMS-650032) is a potent hepatitis C virus (HCV) NS3 protease inhibitor.An inhibitor of the viral enzyme serine protease HCV NS3.

Asunaprevir (BMS-650032) is a potent hepatitis C virus (HCV) NS3 protease inhibitor.An inhibitor of the viral enzyme serine protease HCV NS3.

Biochem/physiol Actions AT1 is a cell penetrant Proteolysis Targeting Chimera (PROTAC) that selectively targets BET4 proteins for degradation by recruitments of ubiquitin E3 ligase. AT1 comprise (+)-JQ1 as a BET4 binding domain and E3 ligase