Title of article :
[3H]-MRE 2029-F20, a selective antagonist radioligand for the human A2B adenosine receptors
Author/Authors :
Pier Giovanni Baraldi، نويسنده , , Mojgan Aghazadeh Tabrizi، نويسنده , , Delia Preti، نويسنده , , Andrea Bovero، نويسنده , , Francesca Fruttarolo، نويسنده , , Romeo Romagnoli، نويسنده , , Allan R. Moorman، نويسنده , , Stefania Gessi، نويسنده , , Stefania Merighi، نويسنده , , Katia Varani، نويسنده , , Pier Andrea Borea، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Abstract :
MRE 2029-F20 [N-benzo[1,3]dioxol-5-yl-2-[5-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-1-methyl-1H-pyrazol-3-yloxy]-acetamide] is a selective antagonist ligand of A2B adenosine receptors. For use as a radioligand, 1,3-diallyl-xanthine, the precursor of [3H]-MRE 2029-F20, was synthesized, and tritiated on the allyl groups. [3H]-MRE 2029-F20 bound to human A2B receptors expressed in CHO cells showed a KD value of 1.65 ± 0.10 nM and Bmax value of 36 ± 4 fmol/mg protein. [3H]-MRE2029-F20 represents a useful tool for the pharmacological characterization of human A2B adenosine receptor subtype.
Keywords :
Radioligand , Pharmacological characterization. , Selective antagonist , Adenosine receptors
Journal title :
Bioorganic & Medicinal Chemistry Letters
Journal title :
Bioorganic & Medicinal Chemistry Letters