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pro vyhledávání: '"Parasympatholytic Activity"'
Akademický článek
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Publikováno v:
Archiv der Pharmazie. 309:735-741
Um die durch Photolyse entstehenden Spaltprodukte von parasympatholytisch wirkenden Xanthen-9-carbonsaureester-Derivaten durch Modellverbindungen identifizieren zu konnen, versuchten wir die Herstellung von Hydroxydixanthen nach Schonberg und Mustafa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65d82d84efd0a2a6b42cea466d6721af
https://doi.org/10.1002/ardp.19763090910
https://doi.org/10.1002/ardp.19763090910
Publikováno v:
Journal of Medicinal Chemistry. 27:1347-1350
Thirty amides patterned after the antiarrhythmic drug changrolin were synthesized and their antiarrhythmic and parasympatholytic activities were assessed. There was no correlation between antiarrhythmic and parasympatholytic activities. Several of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93754f251edd542c7a0bfa210aa09ca2
https://doi.org/10.1021/jm00376a022
https://doi.org/10.1021/jm00376a022
Publikováno v:
Journal of Medicinal Chemistry. 28:295-298
As part of a continuing program of systematically modifying the structure of the class I antiarrhythmic drug changrolin, we synthesized 15 analogues in which the linkage between the two aromatic regions was altered. High antiarrhythmic activity and l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fad73c1ee6f6dddf0d93040c93e5158
https://doi.org/10.1021/jm00381a006
https://doi.org/10.1021/jm00381a006
Publikováno v:
Chemischer Informationsdienst. 16
As part of a continuing program of systematically modifying the structure of the class I antiarrhythmic drug changrolin, we synthesized 15 analogues in which the linkage between the two aromatic regions was altered. High antiarrhythmic activity and l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21fcce85253c05b5b81ad5e22b0beda1
https://doi.org/10.1002/chin.198532153
https://doi.org/10.1002/chin.198532153
Publikováno v:
Journal of medicinal and pharmaceutical chemistry. 1(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a74a48f6c163d76b16aa1af94aefbdc6
https://pubmed.ncbi.nlm.nih.gov/13665290
https://pubmed.ncbi.nlm.nih.gov/13665290
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas, 8, 91, 989-1001
The preparation and muscarinic activities of a number of 5-alkyl substituted analogues of the dioxolane of Fourneau are described. Muscarinic activity decreases rapidly when the alkyl chain lengthens, moreover a change from parasympathomimetic into p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4008af73134335b0d58ae4cc384d5bb2
http://resolver.tudelft.nl/uuid:8a890f57-780d-48db-b7db-c8304fce39f3
http://resolver.tudelft.nl/uuid:8a890f57-780d-48db-b7db-c8304fce39f3
Autor:
Roger Rittenhouse, Ralph J. Fessenden
Publikováno v:
Journal of medicinal chemistry. 11(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eac3b54a2a8efa89af515e0b1517b2f
https://pubmed.ncbi.nlm.nih.gov/5697075
https://pubmed.ncbi.nlm.nih.gov/5697075