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[N-[2-(p-Bromocinnamylamino)ethyl]-5-isoquinoline sulfonamide, Di-HCl Salt]
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Size |
US $ |
€ |
£ |
¥ |
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10 mg |
57 |
47 |
31 |
6800 |
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25 mg |
119 |
99 |
65 |
14300 |
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100 mg |
399 |
331 |
219 |
47900 |
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300 mg |
975 |
809 |
536 |
117000 |
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M.W. 519.29
C20H20BrN3O2S2HCl
[127243-85-0]
Storage: Store desiccated at or below -20 ºC. Solubility: Soluble in DMSO, water (up to 25 mg/mL; heat to dissolve), or ethanol/water. Disposal: A
View the MSDS for this product
Potent and selective inhibitor of PKA, with an IC50 of about 50 nM. Chijiwa, T., et al. "Inhibition of forskolin-induced neurite outgrowth and protein phosphorylation by a newly synthesized selective inhibitor of cyclic AMP-dependent protein kinase, N-[2-(p-bromocinnamylamino)ethyl]-5-isoquinolinesulfonamide (H-89), of PC12D pheochromocytoma cells." J. Biol. Chem. 265: 5267-5272 (1990).
Also inhibits PKG and the µ isotype of PKC (at about 500 nM). In contrast, most other PKC isotypes are much more weakly inhibited, with IC50's in the 32 µM range. Johannes, F.-J., Prestle, J., Dieterich, S., Oberhagemann, P., Link, G. and Pfizenmaier, K. "Characterization of activators and inhibitors of protein kinase Cµ." Eur. J. Biochem. 227: 303-307 (1995).
Please request Technical Note #24 for additional information.
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