1. Stem Cell/Wnt TGF-beta/Smad Metabolic Enzyme/Protease
  2. PKA Phosphodiesterase (PDE)
  3. Sp-cAMPS triethylamine

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

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Sp-cAMPS triethylamine

Sp-cAMPS triethylamine 화학구조

CAS No. : 93602-66-5

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  • Biological Activity

  • 순도&문서

  • References

  • 고객리뷰

제품 설명

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

IC50 & Target[2][3]

PKA I

 

PKA II

 

PDE3A

47.6 μM (Ki)

PDE10 GAF domain

50 μM (EC50)

In Vitro

Treatment of hepatocytes with Sp-cAMPS triethylamine, the stimulatory diastereomer of adenosine cyclic 3',5'-phosphorothioate, mimics the response seen with glucagon. The glucagon-stimulated increases in the level of Ca2+ can be mimicked by Sp-cAMPS triethylamine[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

In chronic alcohol consumption (CAC) mice, direct infusion of the Sp-cAMPS (1 µg/µL) triethylamine into the prefrontal cortex significantly improves or impairs, respectively, working memory performance in withdrawn and water animals[5].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

분자량

446.46

화학식

C16H27N6O5PS

CAS No.
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

선적

Room temperature in continental US; may vary elsewhere.

보관

Please store the product under the recommended conditions in the Certificate of Analysis.

순도&문서
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상품명:
Sp-cAMPS triethylamine
Cat. No.:
HY-110005
수량:
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