VUF 5574

VUF 5574

CAT N°: 27676
Price:

From 48.00 40.80

VUF 5574 is an antagonist of the adenosine A3 receptor (Ki = 4.03 nM for the recombinant human receptor).{49476} It is greater than 2,500-fold selective for adenosine A3 over A1 and A2A receptors. VUF 5574 (100 nM) decreases phosphorylation of ERK1/2 induced by adenosine (Item No. 21232) in isolated porcine coronary artery smooth muscle cells.{49477} It increases oxygen-glucose deprivation-induced reductions in the amplitude of field excitatory postsynaptic potentials (EPSPs) in a rat hippocampal slice model of ischemia when used at a concentration of 100 nM.{49478} VUF 5574 (2 µg, intracisternal) reduces sodium nitroprusside-induced heart rate increases in rats.{49479}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • N-(2-methoxyphenyl)-N’-[2-(3-pyridinyl)-4-quinazolinyl]-urea
  • Correlated keywords
    • VUF5574 A-3 1 2A ERK 1/2 post synaptic
  • Product Overview:
    VUF 5574 is an antagonist of the adenosine A3 receptor (Ki = 4.03 nM for the recombinant human receptor).{49476} It is greater than 2,500-fold selective for adenosine A3 over A1 and A2A receptors. VUF 5574 (100 nM) decreases phosphorylation of ERK1/2 induced by adenosine (Item No. 21232) in isolated porcine coronary artery smooth muscle cells.{49477} It increases oxygen-glucose deprivation-induced reductions in the amplitude of field excitatory postsynaptic potentials (EPSPs) in a rat hippocampal slice model of ischemia when used at a concentration of 100 nM.{49478} VUF 5574 (2 µg, intracisternal) reduces sodium nitroprusside-induced heart rate increases in rats.{49479}

We also advise you