Protease Inhibitors

Application Protein degrader builiding block C5 Lenalidomide-pyrimidine-piperazine-PEG 1 -NH 2 hydrochloride enables the synthesis of molecules for targeted protein degradation and PROTAC (proteolysis-targeting chimeras) technology . This conjugate

Product description：Purity: &gt:90% by SDS-PAGEExtinction Coeff. A280 nm = 1.08 at 1.0 mg/mLMolecular Weight: 105,000 Da (single chain)Precautions: Use normal precautions for handling human blood productsGeneral DescriptionNative human C6 is a

Inhibitor of Cathepsin B.

Inhibitor of Cathepsin B.

Inhibitor of Cathepsin B.

Inhibitor of Cathepsin B.

Inhibitor of Cathepsin B.

Inhibitor of Cathepsin B.

InformationCA-074 methyl ester (CA-074 Me) CA-074 methyl ester (CA-074 Me, Cathepsin B Inhibitor IV) is a membrane-permeable derivative of CA-074 and acts as an irreversible cathepsin B inhibitor.In vitroCA-074Me is able to inhibit cathepsin L

Calpain Inhibitor XII is a cell-permeable, potent, selective, reversible, and active-site-directed inhibitor of calpain-1 (K|i|= 19 nM). Calpain Inhibitor XII has been shown to inhibit calpain-2 (K|i|= 120 nM) and human cathepsin B (K|i|= 750 nM)

Calpain Inhibitor XII is a cell-permeable, potent, selective, reversible, and active-site-directed inhibitor of calpain-1 (K|i|= 19 nM). Calpain Inhibitor XII has been shown to inhibit calpain-2 (K|i|= 120 nM) and human cathepsin B (K|i|= 750 nM)

Calpain Inhibitor XII is a cell-permeable, potent, selective, reversible, and active-site-directed inhibitor of calpain-1 (K|i|= 19 nM). Calpain Inhibitor XII has been shown to inhibit calpain-2 (K|i|= 120 nM) and human cathepsin B (K|i|= 750 nM)