| dc.contributor.author | Şafak, C | |
| dc.contributor.author | Erdoğan, H | |
| dc.contributor.author | Yeşilada, A | |
| dc.contributor.author | Erol, K | |
| dc.contributor.author | Cimgi, I | |
| dc.date.accessioned | 2019-10-22T20:08:16Z | |
| dc.date.available | 2019-10-22T20:08:16Z | |
| dc.date.issued | 1992 | |
| dc.identifier.issn | 0004-4172 | |
| dc.identifier.issn | 1616-7066 | |
| dc.identifier.uri | https://hdl.handle.net/11421/22522 | |
| dc.description | WOS: A1992HD96200009 | en_US |
| dc.description | PubMed ID: 1610420 | en_US |
| dc.description.abstract | In this study 13 new dithiocarbamates were prepared by reacting 3-methyl-6-chloroacetyl-benzoxazolinone with potassium N,N-disubstituted dithiocarbamate derivatives. The structures of the compounds were confirmed by UV, IR, H-1-NMR, mass spectroscopic methods and elementary analysis. The anticholinergic activity was tested on rabbit ileum. With exception of one compound all derivatives exhibited a stronger antihistaminic activity as compared with their anticholinergic action. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Georg Thieme Verlag Kg | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Antihistaminics | en_US |
| dc.subject | Carbamodithioic Acid Esters | en_US |
| dc.subject | Dithiocarbamates, Pharmacology, Synthesis | en_US |
| dc.title | Synthesis and Pharmacology of Some New Carbamodithioic Acid-Esters | en_US |
| dc.type | article | en_US |
| dc.relation.journal | Arzneimittelforschung-Drug Research | en_US |
| dc.contributor.department | Anadolu Üniversitesi, Tıp Fakültesi, Farmakoloji Anabilim Dalı | en_US |
| dc.identifier.volume | 42-1 | en_US |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.startpage | 123 | en_US |
| dc.identifier.endpage | 126 | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US] |
