Cell permeable potent and selective inhibitor of cAMP- and cGMP-dependent protein kinases (PKA, Ki=48nM, and PKG) and protein kinase Cµ (PKCµ). In contrast, most other protein kinase C (PKC) isotypes are much more weakly inhibited. Also inhibits Ca2+/cal
Molekulargewicht:
519.3
Reinheit:
99% (HPLC)
CAS Nummer:
[127243-85-0]
Formel:
C20H20BrN3O2S2HCl
Target-Kategorie:
PKA, PKG, PKD, MLCK, Casein kinase I, CaM kinase II
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