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Rp-cAMPS Inhibitor – Triethylammonium Salt

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS5753834

Rp-cAMPS triethylammonium salt is an analog of cAMP.It acts as a potent, competitive and cell-permeable antagonist of cAMP-induced activation of cAMP-dependent PKA I and II with Kis of 6.05uM and 9.75uM, respectively. More details

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Product Overview

Online Datasheet in PDF
Product Name
Rp-cAMPS triethylammonium salt, Inhibitor
Full Product Name
Rp-cAMPS triethylammonium salt
Product Gene Name
Form/Format
Solid. Powder
Purity/Purification
98.00%
Preparation and Storage
Store at -20 degree C for 3 years powder
-80 degree C for 2 years in solvent
Molecular Weight
446.46
Solubility
<1mg/ml refers to the product slightly soluble or insoluble
Formula
C16H27N6O5PS
SMILES
O[C@H]1[C@@H](O[C@@]2([H])[C@@]1([H])O[P@@](OC2)(S)=O)N3C4=C(C(N)=NC=N4)N=C3.CCN(CC)CC
CAS Number
151837-09-1
Target & IC50
PKA I: ic50 6.05uM (ki)
PKA II: ic50 9.75uM (ki)
In Vitro
A membrane-permeable competitive antagonist of cAMP that blocks PKA activation by binding to the regulatory subunits without dissociating the kinase holoenzyme inhibits synaptic plasticity[1].

Structure of Rp-cAMPS, inhibitor

Rp-cAMPS Inhibitor – Cat# MBS5753834

Product References and Citations for Rp-cAMPS, inhibitor

Rothermel JD, et al. A mechanistic and kinetic analysis of the interactions of the diastereoisomers of adenosine 3',5'-(cyclic)phosphorothioate with purified cyclic AMP-dependent protein kinase. Biochem J. 1988 May 1;251(3):757-62.
Rothermel JD, et al. A mechanistic and kinetic analysis of the interactions of the diastereoisomers of adenosine 3',5'-(cyclic)phosphorothioate with purified cyclic AMP-dependent protein kinase. Biochem J. 1988 May 1;251(3):757-62.
Fu Y, et al. PKA and ERK, but not PKC, in the amygdala contribute to pain-related synaptic plasticity and behavior. Mol Pain. 2008 Jul 16;4:26.
Fu Y, et al. PKA and ERK, but not PKC, in the amygdala contribute to pain-related synaptic plasticity and behavior. Mol Pain. 2008 Jul 16;4:26.
Kuriyama S, et al. Isoproterenol inhibits rod outer segment phagocytosis by both cAMP-dependent and independent pathways. Invest Ophthalmol Vis Sci. 1995 Mar;36(3):730-6.
Kuriyama S, et al. Isoproterenol inhibits rod outer segment phagocytosis by both cAMP-dependent and independent pathways. Invest Ophthalmol Vis Sci. 1995 Mar;36(3):730-6.

Other Notes

Small volumes of Rp-cAMPS, inhibitor vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Searchable Terms for Rp-cAMPS purchase

MBS5753834 is an inhibitor targeting Rp-cAMPS. Also known as Rp-cAMPS triethylammonium salt.
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