|Molecular Formula||C16H14ClN5O5PS2 · Na|
|Description||Sp-8-CPT-cAMPS is a selective activator of protein kinase A (cAMP agonist). It effects against mammalian cyclic nucleotide-dependent phosphodiesterases.|
|Purity||≥ 99% by HPLC|
|Synonyms||8- (4- Chlorophenylthio)adenosine- 3', 5'- cyclic monophosphorothioate, Sp- isomer, sodium salt|
6-Phe-cAMP is a selective stimulator of protein kinase A preferring site A of both isozymes.
8-pHPT-2'-O-Me-cAMP is an activator of the exchange protein activated by cAMP (Epac) or cAMP-GEF, which does not activate protein kinase A. It has superior lipo...
8-Br-2'-O-Me-cAMP-AM is a precursor of 8-Br-2'-O-Me-cAMP, the specific Epac agonist. 8-Br-2'-O-Me-cAMP is released after the metabolism of 8-Br-2'-O-Me-cAMP-AM ...
8-pCPT-cGMP-AM is a precursor of 8-pCPT-cGMP, the PKG activator. 8-pCPT-cGMP is released after the metabolism of 8-pCPT-cGMP-AM by esterases.
Sp-8-PIP-cAMPS is a selective cAMP analogue with a preference for site B of protein kinase A type II.
Rp-5,6-DCl-cBIMPS is a phosphodiesterase-resistant regulator of cAMP-dependent protein kinase.
4-MB-cCMP is an analogue of cCMP, the putative second messenger nucleotide and the main cellular metabolite of DB-cCMP. 4-MB-cCMP exhibits a partial activity of...
6-AH-cAMP is a ligand in affinity chromatography of cAMP and cGMP binding proteins and can be modified with fluorophores and other markers.