A potent, cell-permeable, reversible, and ATP-competitive, and highly active inhibitor of cyclic-nucleotide-dependent protein kinases. Inhibits myosin light chain kinase (Ki = 68 µM), protein kinase A (Ki = 1.2 µM), protein kinase C (Ki = 15 µM), and protein kinase G (Ki = 480 nM).
Biochem/physiol Actions
Cell permeable: yes
Product competes with ATP.
Reversible: yes
Target Ki: 68 µM against MLCK
Warning
Toxicity: Standard Handling (A)
Preparation Note
Further dilute with aqueous buffer just prior to use.
Other Notes
Ido, M., et al. 1991. Br. J. Cancer 64, 1103. Hagiwara, M., et al. 1987. Mol. Pharmacol. 31, 523. Inagaki, M., et al. 1986. Mol. Pharmacol.29, 577. Hidaka, H., et al. 1984. Biochemistry23, 5036.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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