cAMPS-Rp, triethylammonium salt, Tocris Bioscience™

Description

cAMP antagonist

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

• 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
• Percent Purity: >98%
• Chemical Name or Material: cAMPS-Rp, triethylammonium salt