| Literature DB >> 17994651 |
Gülhan Turan-Zitouni1, Zafer Asim Kaplancikli, Ahmet Ozdemir, Pierre Chevallet, Hilmi Burak Kandilci, Bülent Gümüsel.
Abstract
The reaction of acetic or propionic acid hydrazides with various aryl/alkyl isothiocyanates gave thiosemicarbazides which furnished the 1,2,4-triazoles by alkali cyclization. The 4-aryl/alkyl-5-(1-phenoxyethyl)-3-[N-(substituted)acetamido]thio-4H-1,2,4-triazole derivatives were synthesized by reacting the triazoles with 2-chloro-N-(substituted)acetamide. The chemical structures of the compounds were elucidated by IR, (1)H-NMR, FAB(+)-MS spectral data and elemental analysis. In the pharmacological studies, anti-inflammatory activities of these compounds have been screened and significant activities were observed.Entities:
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Year: 2007 PMID: 17994651 DOI: 10.1002/ardp.200700134
Source DB: PubMed Journal: Arch Pharm (Weinheim) ISSN: 0365-6233 Impact factor: 3.751