The nonselective antagonist EFA (10 μM) blocked the NECA (100 nM) effect (A) and so did DPCPX at 10 μM, a concentration high enough to block A2BAR (B). In contrast, the A2A selective antagonist SCH 58261 (C) and the A3 selective antagonist MRS 1220 (D), both at 10 μM, had no effect. Western blots show a representative experiment, the columns represent mean values of n = 8 (A), 6 (B), 4 (C), and 5 (D) independent experiments (* p < 0.001, significantly different from control).</p
The effect of 100 μM UTP was consistently lower than of 100 nM NECA. Addition of 30 nM forskolin to ...
A3 Adenosine receptors are promising drug targets for a number of diseases and intense efforts are d...
A3 Adenosine receptors are promising drug targets for a number of diseases and intense efforts are d...
(A) NECA reduced the ERK1/2 phosphorylation in a concentration-dependent manner (EC50 5.85 nM, 95% c...
<p>The particular adenosine receptor subtype involved in profibrotic activation was recognized by us...
Preincubation (30 min) of MDA-MB-231 cells with 10 μM of the PKA inhibitors H-89 prevented the NECA ...
The effect of 100 nM NECA on ERK1/2 phosphorylation was mimicked by compounds increasing intracellul...
The inhibition of ERK1/2 phosphorylation by NECA was blocked by 10 μg/ml of cycloheximide (CHX) sugg...
A time-dependent inhibition of phosphorylation of c-Raf at S338 is observed by stimulation of the A2...
<p>A, Bath application of adenosine (100 µM) reversibly inhibited the evoked AMPA EPSCs (n = 15, p<0...
Background: In this study, the effects of three structural analogues of adenosine upon proliferation...
A number of 2-substituted 5'-N-ethylcarboxamidoadenosine (NECA) derivatives was investigated for the...
A number of 2-substituted 5'-N-ethylcarboxamidoadenosine (NECA) derivatives was investigated for the...
A number of 2-substituted 5'-N-ethylcarboxamidoadenosine (NECA) derivatives was investigated for the...
A number of 2-substituted 5'-N-ethylcarboxamidoadenosine (NECA) derivatives was investigated for the...
The effect of 100 μM UTP was consistently lower than of 100 nM NECA. Addition of 30 nM forskolin to ...
A3 Adenosine receptors are promising drug targets for a number of diseases and intense efforts are d...
A3 Adenosine receptors are promising drug targets for a number of diseases and intense efforts are d...
(A) NECA reduced the ERK1/2 phosphorylation in a concentration-dependent manner (EC50 5.85 nM, 95% c...
<p>The particular adenosine receptor subtype involved in profibrotic activation was recognized by us...
Preincubation (30 min) of MDA-MB-231 cells with 10 μM of the PKA inhibitors H-89 prevented the NECA ...
The effect of 100 nM NECA on ERK1/2 phosphorylation was mimicked by compounds increasing intracellul...
The inhibition of ERK1/2 phosphorylation by NECA was blocked by 10 μg/ml of cycloheximide (CHX) sugg...
A time-dependent inhibition of phosphorylation of c-Raf at S338 is observed by stimulation of the A2...
<p>A, Bath application of adenosine (100 µM) reversibly inhibited the evoked AMPA EPSCs (n = 15, p<0...
Background: In this study, the effects of three structural analogues of adenosine upon proliferation...
A number of 2-substituted 5'-N-ethylcarboxamidoadenosine (NECA) derivatives was investigated for the...
A number of 2-substituted 5'-N-ethylcarboxamidoadenosine (NECA) derivatives was investigated for the...
A number of 2-substituted 5'-N-ethylcarboxamidoadenosine (NECA) derivatives was investigated for the...
A number of 2-substituted 5'-N-ethylcarboxamidoadenosine (NECA) derivatives was investigated for the...
The effect of 100 μM UTP was consistently lower than of 100 nM NECA. Addition of 30 nM forskolin to ...
A3 Adenosine receptors are promising drug targets for a number of diseases and intense efforts are d...
A3 Adenosine receptors are promising drug targets for a number of diseases and intense efforts are d...