|Molecular Formula||C10H11N5O6PS · Na|
|Description||Sp-8-OH-cAMPS is a polar analogue of Sp-cAMPS, the protein kinase A activator, with an antagonistic effect of mammalian cyclic nucleotide-dependent phosphodiesterases. It can be used for the study of extracellular cAMP receptors.|
|Purity||≥ 99% by HPLC|
|Synonyms||8- Hydroxyadenosine- 3', 5'- cyclic monophosphorothioate, Sp- isomer, sodium salt|
2'd-7-CH-ATP is an isosteric modification of dATP.
6-Phe-cAMP is a selective stimulator of protein kinase A preferring site A of both isozymes.
Sp-8-pCPT-PET-cGMPS is an activator of cyclic GMP-dependent protein kinase as well as an inhibitor of the retinal type cGMP-gated ion channel, thus it can be us...
2'-dcGMP is an analogue of cGMP, which is a protein kinase G inactive agent.
Rp-8-OH-cAMPS is a polar analogue of Rp-cAMPS, the protein kinase A inhibitor, used for the study of extracellular cAMP receptors. It inhibits mammalian cyclic ...
2-NH2-cPuMP is a fluorescent cyclic nucleotide (λexc305 nm; λem370 nm) used in receptor mapping studies.
4-N-cBIMP is an analogue of cAMP, the second messenger, which has a changed interaction potential at position 6.