1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDE
1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDE Basic information
- Product Name:
- 1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDE
- Synonyms:
-
- 1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDE
- CATHEPSIN K INHIBITOR III
- INHIBITOR I
- Z-L-NHNHCONHNH-LF-NH2
- MF:
- C30H43N7O6
- MW:
- 597.71
- Mol File:
- Mol File
1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDE Chemical Properties
- storage temp.
- -20°C
- solubility
- DMSO: 1mg/mL
- form
- lyophilized solid
- color
- white
1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDE Usage And Synthesis
Uses
A cell-permeable peptidyl bis-carbohydrazide compound that acts as a potent, selective, and reversible inhibitor of cathepsin K (Ki,app = 9.7 nM). At higher concentrations, also inhibits the activities of cathepsin L, cathepsin B, and papain (Ki,app = 120 nM, 5.1 µM, and 2.3 µM, respectively). Completely blocks cathepsin K activity in primary human synovial fibroblast cultures at 1 µM.
A cell-permeable, potent, selective, reversible inhibitor of cathepsin K (Ki,app = 9.7 nM). At higher concentrations also inhibits the activities of cathepsin L, cathepsin B, and papain (Ki,app = 120 nM, 5.1 mM, and 2.3 µM, respectively). Reported to completely block cathepsin K activity in primary human synovial fibroblast cultures at a concentration of 1 µM.
Biological Activity
Cell permeable: yes', 'Primary Target
Cathepsin K', 'Product does not compete with ATP.', 'Reversible: yes', 'Target Ki: 9.7 nM against cathepsin K