219381
Cathepsin K Inhibitor III
The Cathepsin K Inhibitor III controls the biological activity of Cathepsin K. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.
동의어(들):
Cathepsin K Inhibitor III, Inhibitor I, 1-(N-Benzyloxycarbonyl-leucyl)-5-(phenylalanyl-leucyl)carbohydrazide, Z-L-NHNHCONHNH-LF-NH₂
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모든 사진(1)
About This Item
추천 제품
Quality Level
분석
≥97% (HPLC)
형태
lyophilized solid
제조업체/상표
Calbiochem®
저장 조건
OK to freeze
desiccated (hygroscopic)
색상
white
solubility
DMSO: 1 mg/mL
배송 상태
wet ice
저장 온도
−20°C
일반 설명
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.
생화학적/생리학적 작용
Cell permeable: yes
Primary Target
Cathepsin K
Cathepsin K
Product does not compete with ATP.
Reversible: yes
Target Ki: 9.7 nM against cathepsin K
포장
Packaged under inert gas
경고
Toxicity: Standard Handling (A)
서열
H-Phe-Leu-NHNH-CO-NHNH-Leu-Z
물리적 형태
Supplied as a trifluoroacetate salt.
재구성
Following reconstitution aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
기타 정보
Wang, D., et al. 2002. Biochemistry41, 8849.
법적 정보
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
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