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Cat. No. Product Name Information
PC-42147

Odanacatib

Cathepsin K inhibitor

Odanacatib (MK-0822) is a potent, selective, reversible and orally active cathepsin K inhibitor with IC50 of 0.2 nM.
PC-45577

MG-101

Cysteine proteases inhibitor

MG-101 (ALLN) is a potent inhibitor of cysteine proteases including calpain I (Ki= 190 nM), calpain II (Ki= 220 nM), cathepsin B (Ki= 150 nM) and cathepsin L (Ki= 500 pM).
PC-22251

JNJ-10311795

Cathepsin G inhibitor

JNJ-10311795 is a potent dual inhibitor of neutrophil cathepsin G (Ki=38 nM) and mast cell chymase (Ki=2.3 nM), exhibits noteworthy anti-inflammatory activity in rats for glycogen-induced peritonitis and LPS-induced airway inflammation.
PC-22250

Cathepsin G inhibitor KPA

Cathepsin G inhibitor

Cathepsin G inhibitor KPA is a potent, selective, reversible, competitive, non-peptide inhibitor of cathepsin G (CatG) with IC50 of 53 nM.
PC-22165

ASP1617

Cathepsin S inhibitor

ASP1617 (ASP-1617) is a potent, highly specific and orally active cathepsin S (CatS) inhibitor with IC50 of 4.6 nM and 0.39 nM for human and mouse CatS, respectively.
PC-22164

RO5461111

Cathepsin S inhibitor

RO5461111 is a potent, highly specific and orally active cathepsin S (CatS) inhibitor with IC50 of 0.4 nM and 0.5 nM for human and mouse CatS respectively.
PC-21937

Balicatib

Cathepsin K inhibitor

Balicatib (AAE581) is a potent, selective and orally active and selective cathepsin K inhibitor with IC50 of 22 nM.
PC-21936

CA-074

Cathepsin B inhibitor

CA-074 is a potent, specific and cell-permeable inhibitor of cathepsin B with Ki of 2-5 nM.
PC-21763

VBY-825

Cathepsin S inhibitor

VBY-825 is an reversible cathepsin inhibitor of cathepsins B, L, S and V.with Ki values of 130/250/250/330/2.3/4.7 nM (cathepsin S/L/ZV/Bhumanized-rabbit cathepsin K/cathepsin F).
PC-20410

Z-Tyr-Ala-CHN2

Cathepsin L inhibitor

Z-Tyr-Ala-CHN2 is a potent cathepsin L inhibitor with EC50 of <50 nM, has broad-spectrum coronavirus antiviral activity.
PC-20203

Dutacatib

Cathepsin K inhibitor

Dutacatib (AFG495) is potent, selective and non-covalent cathepsin K inhibitor with IC50 of 3-6 nM (human CatK), shows excellent selectivity profile versus human cathepsins L and S.
PC-38582

SID 26681509

Cathepsin L inhibitor

SID 26681509 is a potent, selective inhibitor of lysosome hydrolase cathepsin L with IC50 of 56 nM, displays no inhibitory activity at cathepsin G.

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