Novel and highly selective postsynaptic α-adrenoreceptor antagonists: synthesis and structure-activity relationships of alkane-bridged [4-(phenoxyethyl)-1-piperazinyl]-3(2H)-pyridazinones
- 31 December 1995
- journal article
- research article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 30 (1) , 71-75
- https://doi.org/10.1016/0223-5234(96)88211-0
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- New pyridazinones: synthesis and correlation between structure and α-blocking activityEuropean Journal of Medicinal Chemistry, 1993
- Synthesis and pharmacological activity of some new pyridazinonesEuropean Journal of Medicinal Chemistry, 1992
- In-vitro evaluation of filaricidal activity of GABA and 1,3-dipalmitoyl-2-(4-aminobutyryl)glycerol HCl: a diglyceride prodrugJournal of Pharmacy and Pharmacology, 1989
- GYKI-12743Drugs of the Future, 1989
- 4(And 5)‐cyclopropylamino‐5(and 4)halo‐3(2H)pyridazinones. Formation and characterization of isomersJournal of Heterocyclic Chemistry, 1977
- SELECTIVITY OF BLOCKING AGENTS FOR PRE‐ AND POSTSYNAPTIC α‐ADRENOCEPTORSBritish Journal of Pharmacology, 1977
- Pharmacological characterisation of the presynaptic α-adrenoceptor in the rat vas deferensEuropean Journal of Pharmacology, 1977
- Mucochloric Acid. II. Reactions of the Aldehyde Group1Journal of the American Chemical Society, 1953