The Adenosine A2A/A1 Receptor Antagonist controls the biological activity of Adenosine A2A/A1 Receptor. This small molecule/inhibitor is primarily used for Biochemicals applications.
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Adenosine A 2A/A1 Receptor Antagonist
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Adenosine A 2A/A1 Receptor Antagonist, The Adenosine A2A/A1 Receptor Antagonist controls the biological activity of Adenosine A2A/A1 Receptor. This small molecule/inhibitor is primarily used for Biochemicals applications.
A blood-brain barrier-permeant indenopyrimidinone that acts as a dual A1/A2A antagonist (Ki = 48.2 and 6.5 nM, respectively, against agonist-induced cAMP response in A1- or A2A-expressing CHO-K1 cells) and effectively reverses D2 antagonist haloperidol- (1 mg/kg; s.c.) induced catalepsy in both rats and mice (ED50 = 0.3 and <0.1 mg/kg, respectively) in vivo by simultaneously reversing A1-mediated inhibition of DA (Dopamine) release and A2A-dependent inhibition of D2 receptor response to DA.
The Adenosine A2A/A₁ Receptor Antagonist controls the biological activity of Adenosine A2A/A₁ Receptor. This small molecule/inhibitor is primarily used for Biochemicals applications.
Other Notes
Shook, B.C., et al. 2012. J. Med. Chem.55, 1402.
Packaging
Packaged under inert gas
Preparation Note
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Classe di stoccaggio
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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