| Literature DB >> 12403303 |
Maria Dobosz1, Marta Struga, Anna Chodkowska, Ewa Jagiełło-Wójtowicz, Krystyna Stepniak, Anna E Kozioł.
Abstract
In the reaction of (4-phenyl- or 3,4-diphenyl-5-oxo-1,2,4-triazeolin-1-ylmethyl)-carbohydrazide (IIa, IIb) with isothiocyanates the thiosemicarbazide derivatives [IIIa, b - IXa, b] were obtained. Cyclization of those compounds in the presence of 2% or 10% NaOH led to formation of derivatives with the 1,2,4-triazolin-5-thione system [Xa, b - XV[a, b]. Molecular structure proposed for this group of compounds was confirmed by X-ray structure analysis of Xa and XIVa. Compounds Xa, XIIa and XIVa were investigated pharmacologically for their central properties in mice. It was shown that only compound XIIa produced antinociceptive effects in mice.Entities:
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Year: 2002 PMID: 12403303
Source DB: PubMed Journal: Acta Pol Pharm ISSN: 0001-6837 Impact factor: 0.330