Urapidil and some analogues with hypotensive properties show high affinities for 5-hydroxytryptamine (5-HT) binding sites of the 5-HT1A subtype and for α1-adrenoceptor binding sites
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Veröffentlicht in: | Naunyn-Schmiedeberg's archives of pharmacology 1987-12, Vol.336 (6), p.597-601 |
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container_issue | 6 |
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container_title | Naunyn-Schmiedeberg's archives of pharmacology |
container_volume | 336 |
creator | GROSS, G HANFT, G KOLASSA, N |
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doi_str_mv | 10.1007/BF00165749 |
format | Article |
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identifier | ISSN: 0028-1298 |
ispartof | Naunyn-Schmiedeberg's archives of pharmacology, 1987-12, Vol.336 (6), p.597-601 |
issn | 0028-1298 1432-1912 |
language | eng |
recordid | cdi_pascalfrancis_primary_7849791 |
source | SpringerNature Journals |
subjects | Antihypertensive agents Biological and medical sciences Cardiovascular system Medical sciences Pharmacology. Drug treatments |
title | Urapidil and some analogues with hypotensive properties show high affinities for 5-hydroxytryptamine (5-HT) binding sites of the 5-HT1A subtype and for α1-adrenoceptor binding sites |
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