cAMP: Small Molecules and Peptides
cAMP (adenosine 3’5’-cyclic monophosphate) is a ubiquitous intracellular second messenger that mediates a diverse range of cellular processes in all organisms from bacteria to higher eukaryotes. It is converted from adenosine triphosphate (ATP) by adenylyl cyclases (ACs), and is inactivated by phosphodiesterases (PDEs) which catalyze its hydrolysis to 5’-AMP.
In mammals, upon interaction with extracellular ligands, G protein coupled receptors (GPCRs) linked to Gαs activate the family of nine transmembrane ACs to increase intracellular cAMP. In contrast, GPCRs associated with Gαi/o inhibit the synthesis of cAMP by transmembrane ACs. cAMP binds and activates protein kinase A (PKA), the guanine nucleotide exchange factors Epac1/2, and cyclic nucleotide-gated ion channels. It can be released extracellularly where it is converted to adenosine by phosphodiesterases and nucleotidases.
Products:
6 results for "cAMP Small Molecules and Peptides" in Products
6 results for "cAMP Small Molecules and Peptides" in Products
cAMP: Small Molecules and Peptides
cAMP (adenosine 3’5’-cyclic monophosphate) is a ubiquitous intracellular second messenger that mediates a diverse range of cellular processes in all organisms from bacteria to higher eukaryotes. It is converted from adenosine triphosphate (ATP) by adenylyl cyclases (ACs), and is inactivated by phosphodiesterases (PDEs) which catalyze its hydrolysis to 5’-AMP.
In mammals, upon interaction with extracellular ligands, G protein coupled receptors (GPCRs) linked to Gαs activate the family of nine transmembrane ACs to increase intracellular cAMP. In contrast, GPCRs associated with Gαi/o inhibit the synthesis of cAMP by transmembrane ACs. cAMP binds and activates protein kinase A (PKA), the guanine nucleotide exchange factors Epac1/2, and cyclic nucleotide-gated ion channels. It can be released extracellularly where it is converted to adenosine by phosphodiesterases and nucleotidases.
Products:
Cell-permeable cAMP analog
| Alternate Names: | Bucladesine sodium |
| Chemical Name: | N6,O2'-Dibutyryladenosine 3',5'-cyclic monophosphate sodium salt |
| Purity: | ≥98% (HPLC) |
Cell-permeable cAMP analog
| Chemical Name: | 8-Bromoadenosine-3',5'-cyclic monophosphate sodium salt |
| Purity: | ≥99% (HPLC) |
Cell permeable cAMP analog
| Chemical Name: | N-Benzoyladenosine cyclic 3',5'-(hydrogen phosphate) monosodium salt |
| Purity: | ≥98% (HPLC) |
cAMP antagonist
| Chemical Name: | (R)-Adenosine, cyclic 3',5'-(hydrogenphosphorothioate) triethylammonium |
| Purity: | ≥98% (HPLC) |
Cell-permeable cAMP analog
| Chemical Name: | (S)-Adenosine, cyclic 3',5'-(hydrogenphosphorothioate) triethylammonium |
| Purity: | ≥98% (HPLC) |
Potent and selective CFTR potentiator
| Chemical Name: | N-[2,4-Bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxo-3-quinolinecarboxamide |
| Purity: | ≥98% (HPLC) |
