Home   >  
Protease/Metabolic Enzyme
  • Protease/Metabolic Enzyme
  >  
Cathepsin

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

Cathepsin

Chemical Structure Cat. No. Product Name CAS No.
NSC 185058 Chemical Structure
BCP30689 NSC 185058 39122-38-8
NSC 185058 is an inhibitor of ATG4B, a major cysteine protease. NSC185058 markedly attenuates autophagic activity.
Petesicatib Chemical Structure
BCP30532 Petesicatib 1252637-35-6
Petesicatib is a cathepsin inhibitor drug candidate.
Z-Phe-Tyr(tBu)-diazomethylketone Chemical Structure
BCP29942 Z-Phe-Tyr(tBu)-diazomethylketone 114014-15-2
Z-Phe-Tyr(tBu)-diazomethylketone is an irreversible cathepsin L inhibitor which is ca 10'000 times more effective in inactivating cathepsin L than cathepsin S.
Z-Gly-Leu-Phe-CMK Chemical Structure
BCP23532 Z-Gly-Leu-Phe-CMK Z-Gly-Leu-Phe-CMK
Z-Gly-Leu-Phe-CMK is a cathepsin G inhibitor.
Balicatib Chemical Structure
BCP09098 Balicatib 354813-19-7
Balicatib, an inhibitor of the osteoclastic enzyme cathepsin K.
Leupeptin hemisulfate anhydrous Chemical Structure
BCP10660 Leupeptin hemisulfate anhydrous 103476-89-7
Leupeptin is a reversible inhibitor of protease with Ki values of 35 nM, 3.4 μM, 6 nM and 72 nM for bovine trypsin, human plasmin, bovine spleen cathepsin B and recombinant human calpain, respectively.
MDL28170 Chemical Structure
BCP15636 MDL28170 88191-84-8
MDL 28170 is a selective inhibitor, which inhibites calpain with Ki values of 10nM and cathepsin B with Ki values of 25 nM while does not inhibit trypsin-like serine proteases.
Odanacatib Chemical Structure
BCP01830 Odanacatib 603139-19-1
Odanacatib (MK 0822) is an inhibitor of cathepsin K with potential anti-osteoporotic activity.
Cathepsin Inhibitor 1 Chemical Structure
BCP06025 Cathepsin Inhibitor 1 225120-65-0
Cathepsin Inhibitor 1 is an inhibitor of Cathepsin (L, L2, S, K, B) with pIC50 of 7.9, 6.7, 6.0, 5.5 and 5.2, respectively.
LY3000328 Chemical Structure
BCP14297 LY3000328 1373215-15-6
LY 3000328 is a potent and selective Cathepsin S (Cat S) inhibitor with IC50 of 7.7±5.85 nM and 1.67±1.17 nM for hCat S and mCat S.
12下一页共 14 条记录 1 / 2 页 
0086-15971444841