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U 0521

Known as: 1-(3,4-dihydroxyphenyl)-2-methyl-1-propanone, U-0521, U0521 
National Institutes of Health

Papers overview

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2005
2005
SummaryThe sensitivity of various isolated organs to catecholamines was tested before and after block of catechol-O-methyl… 
2004
2004
SummaryRabbit aortic strips (nerve-free, reserpinepretreated or normal) whose noradrenaline-metabolizing enzymes were inhibited… 
Highly Cited
2004
Highly Cited
2004
Summary1.Isolated rat and guinea-pig hearts were perfused with 0.95 μM (±)-isoprenaline or 3H(±)-isoprenaline, a catecholamine… 
1996
1996
The relative potency of α-adrenoceptor agonists and the dissociation constants of competitive antagonists were studied to… 
1979
1979
1 Transmural stimulation of intrinsic sympathetic nerves and exogenous catecholamines produce β1‐adrenoceptor mediated relaxant… 
1978
1978
Summary1.Rabbit aortic strips were incubated with 1.18 μM 3H-(±)-noradrenaline for 30 min, and the accumulation of noradrenaline… 
1977
1977
SummaryThe effect of 3′,4′-dihydroxy-α-methylpropiophenone (U-0521) on the rate of spontaneously contracting cultured rat heart… 
1976
1976
Summary1.Nerve-free rabbit aortic strips were exposed to 1.18 μM 3H-(±)noradrenaline for 30 min. When either MAO or COMT was…