What is the catalog number for Sp-cAMPS?

The catalog number for Sp-cAMPS is HY-100530B.

What sizes are available for Sp-cAMPS?

Sp-cAMPS is available in the following size(s): 1 Each.

Is Sp-cAMPS in stock?

Sp-cAMPS is currently made to order / not held in immediate stock. Contact us for lead time.

Who manufactures Sp-cAMPS?

Sp-cAMPS is manufactured by QuantiMol.

What is the estimated delivery time for Sp-cAMPS?

Estimated delivery time for Sp-cAMPS is approximately 15 business day(s), depending on your location.

Where can I find the safety data sheet (SDS/MSDS) for Sp-cAMPS?

The safety data sheet for Sp-cAMPS is available here: http://file.medchemexpress.com/batch_PDF/HY-100530B/.

Sp-cAMPS

Sp-cAMPS, a cAMP analog, is potent activator of cAMP-dependent PKA I and PKA II. Sp-cAMPS is also a potent, competitive phosphodiesterase (PDE3A) inhibitor with a Ki of 47.6 µM. Sp-cAMPS binds the PDE10 GAF domain with an EC50 of 40 μM[1][2][3].

Product Specifications

CAS Number

71774-13-5

UNSPSC

12352005

Target

Phosphodiesterase (PDE) ; PKA

Type

Reference compound

Related Pathways

Metabolic Enzyme/Protease; Stem Cell/Wnt; TGF-beta/Smad

Applications

Neuroscience-Neuromodulation

Field of Research

Metabolic Disease; Neurological Disease

Assay Protocol

https://www.medchemexpress.com/sp-camps.html

Solubility

10 mM in DMSO

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

Molecular Formula

C10H12N5O5PS

Molecular Weight

345.27

References & Citations

[1]Su H Hung, et al. A new nonhydrolyzable reactive cAMP analog, (Sp) -adenosine-3',5'-cyclic-S- (4-bromo-2,3-dioxobutyl) monophosphorothioate irreversibly inactivates human platelet cGMP-inhibited cAMP phosphodiesterase. Bioorg Chem. 2002 Feb;30 (1) :16-31.|[2]L Y Wang, et al. Regulation of kainate receptors by cAMP-dependent protein kinase and phosphatases. Science. 1991 Sep 6;253 (5024) :1132-5.|[3]Ronald Jäger, et al. Activation of PDE10 and PDE11 phosphodiesterases. J Biol Chem. 2012 Jan 6;287 (2) :1210-9.|[4]P A Connelly, et al. A study of the mechanism of glucagon-induced protein phosphorylation in isolated rat hepatocytes using (Sp) -cAMPS and (Rp) -cAMPS, the stimulatory and inhibitory diastereomers of adenosine cyclic 3',5'-phosphorothioate. J Biol Chem. 1987 Mar 25;262 (9) :4324-32.|[5]G Dominguez, et al. Rescuing prefrontal cAMP-CREB pathway reverses working memory deficits during withdrawal from prolonged alcohol exposure. Brain Struct Funct. 2016 Mar;221 (2) :865-77.