The adenosine (ADO) receptor in NIH 3T3 fibroblasts was characterized using a series of
adenosine agonists and selected xanthine and non-xanthine antagonists. The ADO receptor …

The effect of several adenosine analogues on cyclic AMP accumulation was examined in
the rat phaeochromocytoma cell PC12 and in the human T-cell leukaemia cell Jurkat …

The xanthines currently represent the most potent class of adenosine receptor antagonists.
However, known derivatives of xanthine show little difference in antagonist potency between …

A2A Adenosine Receptors from Rat Striatum and Rat Pheochromocytoma PC12 Cells:
Characterization with Radioligand Binding and by Activation of Adenylate Cyclase - PMC Back …

We have used the polymerase chain reaction technique to selectively amplify guanine
nucleotide-binding regulatory protein (G protein)-coupled receptor cDNA sequences from rat …

We have cloned and pharmacologically characterized the A2B adenosine receptor (AR)
from the dog, rabbit, and mouse. The full coding regions of the dog and mouse A2BAR were …

Adenosine acting through membrane-bound A1 receptors is capable of inhibiting the
enzyme adenylate cyclase. A1 adenosine receptors from rat cerebral cortex have been …

Adenosine receptors of the A 1, and A 2 subtypes were characterized in membranes from
DDT 1, MF-2 smooth muscle cells. These cells possess a high density of A 1, adenosine …

A newly synthesized, chemically reactive adenosine derivative, N 6-(3-
isothiocyanatobenzyl) adenosine-5′-N-methyluronamide, was found to bind selectively to …

A series of novel and known 5‐substituted 7‐amino‐2‐(2‐furyl)[1, 2, 4] triazolo [1, 5‐a][1, 3,
5] triazine derivatives were synthesized and tested for adenosine receptor antagonism in …