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cAMPS-Rp, triethylammonium salt, Tocris Bioscience™
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Quantity:
1 mg
Description
Cell-permeable cAMP analog; acts as a competitive antagonist of cAMP-induced activation of PKA (IC50 = 11 - 16 μM) by interacting with cAMP binding sites on the regulatory subunits. Resistant to hydrolysis by phosphodiesterases.
Specifications
Specifications
CAS | 151837-09-1 |
Molecular Formula | C16H27N6O5PS |
Quantity | 1 mg |
Synonym | camps-rp, triethylammonium salt, camps-sp, triethylammonium salt, s-adenosine, cyclic 3',5'-hydrogenphosphorothioate triethylammonium, r-adenosine, cyclic 3',5'-hydrogenphosphorothioate triethylammonium |
InChI Key | OXIPZMKSNMRTIV-NVGWRVNNSA-N |
SMILES | CC[NH+](CC)CC.C1C2C(C(C(O2)N3C=NC4=C3N=CN=C4N)O)OP(=S)(O1)[O-] |
IUPAC Name | (4aR,6R,7R,7aS)-6-(6-aminopurin-9-yl)-2-oxido-2-sulfanylidene-4a,6,7,7a-tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-7-ol;triethylazanium |
Molecular Weight (g/mol) | 446.463 |
PubChem CID | 90479783 |
Formula Weight | 446.46 |
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