|M10280||L006235||L006235 (L235) is a potent, reversible cathepsin K inhibitor (IC50 = 0.25 nM) that displays > 4000-fold selectivity over cathepsins B, L and S.|
|M9353||N-Ethylmaleimide||N-Ethylmaleimide (NEM) is a cysteine protease inhibitor.|
|M6236||CA-074 Me||CA-074 Me is a membrane-permeable derivative of CA-074 and acts as an irreversible cathepsin B inhibitor.|
|M5288||UK-371804||UK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibitor with excellent enzyme potency (Ki=10 nM) and selectivity profile (4000-fold versus tPA and 2700-fold versus plasmin).|
|M5167||Calpeptin||Calpeptin is a potent, cell-permeable inhibitor of the Ca2+-dependent protease, calpain.|
|M3826||Papain||Papain is a cysteine protease of the peptidase C1 family.|
|M3636||Leupeptin hemisulfate||Leupeptin hemisulfate is a reversible inhibitor of trypsin-like and cysteine proteases such as calpain.|
|M2600||Balicatib||Balicatib is a potent and selective inhibitor of cathepsin K; 10-100-fold more potent in cell-based enzyme occupancy assays than against cathepsin B, L, and S.|
|M2376||Aloxistatin||Aloxistatin (E64d) is an irreversible and membrane-permeable cysteine protease inhibitor.|
|M1985||Odanacatib||Odanacatib (MK-0822) is an inhibitor of cathepsin K, an enzyme involved in bone resorption.|
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