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cAMPS-Rp, triethylammonium salt, Tocris Bioscience™ Available on GSA/VA Contract for Federal Government customers only.

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Quantity:
1mg
This item is not returnable. View return policy
151837-09-1
C16H27N6O5PS
446.463
OXIPZMKSNMRTIV-NVGWRVNNSA-N
camps-rp, triethylammonium salt,camps-sp, triethylammonium salt,s-adenosine, cyclic 3',5'-hydrogenphosphorothioate triethylammonium,r-adenosine, cyclic 3',5'-hydrogenphosphorothioate triethylammonium
90479783
(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
CC[NH+](CC)CC.C1C2C(C(C(O2)N3C=NC4=C3N=CN=C4N)O)OP(=S)(O1)[O-]
This item is not returnable. View return policy
151837-09-1
C16H27N6O5PS
446.463
OXIPZMKSNMRTIV-NVGWRVNNSA-N
camps-rp, triethylammonium salt,camps-sp, triethylammonium salt,s-adenosine, cyclic 3',5'-hydrogenphosphorothioate triethylammonium,r-adenosine, cyclic 3',5'-hydrogenphosphorothioate triethylammonium
90479783
(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
CC[NH+](CC)CC.C1C2C(C(C(O2)N3C=NC4=C3N=CN=C4N)O)OP(=S)(O1)[O-]

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.

S-enantiomer also available.

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Quantity 1mg
Formula Weight 446.46
Percent Purity >98%
Chemical Name or Material cAMPS-Rp, triethylammonium salt

Recommended Storage : Desiccate at -20°C