Phenoxybenzamine is more potent in inactivating α1- than α2-adrenergic receptor binding sites
- 14 October 1983
- journal article
- research article
- Published by Elsevier in European Journal of Pharmacology
- Vol. 94 (1-2) , 171-174
- https://doi.org/10.1016/0014-2999(83)90458-2
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- [3H]rauwolscine (α-yohimbine): A specific antagonist radioligand for brain α2-adrenergic receptorsEuropean Journal of Pharmacology, 1981
- [125I]BE 2254, a new high affinity radioligand for α1-adrenoceptorsEuropean Journal of Pharmacology, 1981
- Complete blockade by phenoxybenzamine of ?1- but not of ?2-vascular receptors in dogs and the effects of propranololNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1980
- SELECTIVITY OF BLOCKING AGENTS FOR PRE‐ AND POSTSYNAPTIC α‐ADRENOCEPTORSBritish Journal of Pharmacology, 1977
- COMPARISON OF DISSOCIATION CONSTANTS AND OF RELATIVE EFFICACIES OF SELECTED AGONISTS ACTING ON PARASYMPATHETIC RECEPTORS*Annals of the New York Academy of Sciences, 1967
- Receptor Occupancy and Tissue ResponseNature, 1956