Antiepileptic properties of novel 2-(substituted benzylidene)-7-(4-chlorophenyl)-5-(furan-2-yl)-2H-thiazolo[3,2-a]pyrimidin-3(7H)-one derivatives
-
Add time:07/14/2019 Source:sciencedirect.com
In the present study, a series of novel 2-(substituted benzylidene)-7-(4-chlorophenyl)-5-(furan-2-yl)-2H-thiazolo[3,2-a]pyrimidin-3(7H)-one derivatives (4a–i) were designed and synthesized to meet the structural requirements essential for antiepileptic activity. Antiepileptic screening was performed by maximal electroshock (MES) and subcutaneous pentylenetetrazole (scPTZ) seizures tests and neurotoxicity was determined by the rotorod test. Among the synthesized compounds 4f, 4g and 4h were found active in both MES and scPTZ models. In the view of results the most active compounds carry fluoro > chloro > bromo substituent’s at the para position in the phenyl ring. The chemical structures of the synthesized compounds were confirmed by means of IR, 1H NMR, mass spectroscopy and elemental analysis.
We also recommend Trading Suppliers and Manufacturers of [1-(5-Fluoro-pyrimidin-2-yl)-piperidin-4-yl]-methanol (cas 1032825-49-2). Pls Click Website Link as below: cas 1032825-49-2 suppliers
Prev:Follow on-based optimization of the biphenyl-DAPYs as HIV-1 nonnucleoside reverse transcriptase inhibitors against the wild-type and mutant strains
Next:The synthesis, structure and properties of a 1, 2-dihydropyrimidin-2-one formed by UV-irradiation of 5-t-butyl-1-methyluracil) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Follow on-based optimization of the biphenyl-DAPYs as HIV-1 nonnucleoside reverse transcriptase inhibitors against the wild-type and mutant strains07/13/2019
- Identification of highly selective and potent orexin receptor 1 antagonists derived from a dual orexin receptor 1/2 antagonist based on the structural framework of pyrazoylethylbenzamide07/12/2019


