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N-Aralkyl substitution increases the affinity of adrenergic drugs for the alpha-adrenoceptor in rat liver.

1 The alpha-adrenoceptor of rat liver plasma membranes was studied by use of the specific alpha-antagonist [3H]-dihydroergocryptine ([3H]-DHEC). Catecholamines and adrenergic compounds displayed an order of affinity that is typical of an alpha-receptor. Nevertheless, protokylol, a potent beta-adreno...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Aggerbeck, M, Guellaën, G, Hanoune, J
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1979
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1668481/
https://ncbi.nlm.nih.gov/pubmed/216448
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