specially purified quality, fluorescent impurities removed. For other salt forms please inquire. Selective activator of both, cGMP-dependent protein kinase type I α and type II, as well as of cGMP-gated ion channels. Higher activation potential compared to cGMP; excellent cell membrane permeability and stability towards many phosphodiesterases. Recommendable alternative to unsuitable analogues such as dibutyryl cGMP. Detailed technical information and updated reference list available on request. Reference: Geiger et al., Proc. Natl. Acad. Sci. USA, 89, 1031 - 1035 (1992).