Basic information Safety Supplier Related

1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDE

Basic information Safety Supplier Related

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
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1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDE Chemical Properties

storage temp. 
-20°C
solubility 
DMSO: 1mg/mL
form 
lyophilized solid
color 
white
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Safety Information

WGK Germany 
WGK 1
Storage Class
11 - Combustible Solids
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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

1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDESupplier

Merck KGaA
Tel
21-20338288
Email
ordercn@merckgroup.com
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1-(N-BENZYLOXYCARBONYL-LEUCYL)-5-(PHENYLALANYL-LEUCYL)CARBOHYDRAZIDE()Related Product Information