A cell-permeable and reversible calmodulin antagonist that inhibits Ca2+-calmodulin-dependent phosphodiesterase (IC50 = 68 µM) and myosin light chain kinase (IC50 = 58 µM).
A cell-permeable and reversible calmodulin antagonist that inhibits myosin light chain kinase (IC50 = 58 µM) and Ca2+-calmodulin-dependent phosphodiesterase (IC50 = 68 µM).
Biochem/physiol Actions
Target IC50: 58 µM, 68 µM, against myosin light chain kinase and Ca2+-calmodulin-dependent phosphodiesterase
Warning
Toxicity: Standard Handling (A)
Analysis Note
single spot by TLC
Other Notes
Hidaka, H., and Tanaka, T. 1983. Methods Enzymol. 102, 185. Tanaka, T., et al. 1983. Pharmacol.26, 249. Tanaka, T., and Hidaka, H. 1980. J. Biol. Chem. 255, 11078.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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