8- (4- Chlorophenylthio)- ß- phenyl- 1, N²- ethenoguanosine- 3', 5'- cyclic monophosphorothioate, Sp- isomer ( Sp-8-pCPT-PET-cGMPS )

Highly membrane-permeant, PDE-resistant PKG agonist

Cat. No.: C 047   CAS No.: [pending]   
Product Image



C24H18ClN5O6PS2•Na; MW 626.0; λmax 276 nm; ε 40000; sodium salt, purity > 99% HPLC. For other salt forms please inquire. Membrane-permeant activator of cyclic GMP-dependent protein kinase, but most probably inhibitor of the retinal type cGMP-gated ion channel, thus suitable for distinction between kinase and ion channel mediated effects. Resistant against mammalian cyclic nucleotide-dependent phosphodiesterases. More lipophilic and membrane-permeant compared to Sp-8-Br-PET-cGMPS (Cat. No. P 008). Detailed technical information available.

Protected under patents US 5,625,056, DE 42 17679 & DE 3802865.4 issued or licensed exclusively to BIOLOG LSI

 



Forgot your password?
Register
Username:
Password:
What is new!

January 13, 2012

6-Fu-ATP-γ-S reference

Lo & Hollingsworth have successfully used 6-Fu-ATP-γ-S (Cat. No. F 008) from BIOLOG in... [more...]

August 18, 2011

New fluorescent cAMP analogue !

Using the fluorescent cAMP analogue 8-[DY-547]-AET-cAMP (or fcAMP) synthesized by BIOLOG, Ku... [more...]