Membrane permeable analog of cGMP that does not affect cGMP-regulated phosphodiesterase. A more potent cGMP analog than 8-Br-cGMP due to its higher membrane permeability and higher resistance to phosphodiesterase hydrolysis. Acts as a selective activator
Storage Temp
Store at -20°C
Shipped In
Ice chest + Ice pads
Product Description
8-(4-Chlorophenylthio)guanosine 3',5'-cyclic Monophosphate sodium salt (8-CPT-2'-O-Me-cAMP? Na ) is a selective activator of cGKI α, cGKI β, and cGKII (cGMP-dependent protein kinase (PKG) Iα, Iβ, and type II )as well as of CNG (cGMP-gated ion channels). The compounds higher activation potential as compared to cGMP, and retains excellent cell membrane permeability and phosphodiesterase stability. 8-CPT-2'-O-Me-cAMP ? Na has been preferred alternative to unsuitable analogs such as dibutyryl-cGMP.