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dc.contributor.authorAkgün, H.
dc.contributor.authorBalkan, A.
dc.contributor.authorErol, Kevser
dc.contributor.authorBatu, Ö. S.
dc.date.accessioned2019-10-19T14:43:55Z
dc.date.available2019-10-19T14:43:55Z
dc.date.issued1998
dc.identifier.issn0004-4172
dc.identifier.urihttps://hdl.handle.net/11421/13288
dc.descriptionPubMed: 9689423en_US
dc.description.abstractTen new compounds having 7-[(2,4-pentanedione-3-yl)alkyl]- and 7-[(3,5- dimethylisoxazole-4-yl)alkyl]-3,7-dihydro-1,3-dimethyl-1H-purine-2,6-dione structures were synthesized and their bronchodilator activities investigated using the method based on inhibition of acetylcholine and histamine-induced contractions in guinea pig trachea. None of the compounds were effective on acetylcholine-induced contractions. However, the compounds 4d, 4e, 5d and 5c were potent inhibitors of the bronchospasm induced by histamine, whereas the others (4b, 4c, 5b and 5c) were weak inhibitors.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject2,4- Pentanedionesen_US
dc.subject3,5-Dimethylisoxazolesen_US
dc.subjectAntiasthmatic Drugsen_US
dc.subjectAntihistaminic Drugsen_US
dc.subjectTheophylline, Bronchodilator Activityen_US
dc.subjectXanthine Derivativesen_US
dc.titleNew ß-diketone and 3,5-dimethyl isoxazole derivatives of theophylline as potential bronchodilator agentsen_US
dc.typearticleen_US
dc.relation.journalArzneimittel-Forschung/Drug Researchen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmakoloji Anabilim Dalıen_US
dc.identifier.volume48en_US
dc.identifier.issue6en_US
dc.identifier.startpage658en_US
dc.identifier.endpage662en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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