Antidepressant activity of carbamates and urea derivatives |
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Authors: | Shahnaz Perveen Nasreen Fatima Muhammad Aitmaud Khan Ahsana Dar Khalid M. Khan Nighat Afza Wolfgang Voelter |
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Affiliation: | 1. PCSIR Laboratories Complex, Karachi, Shahrah-e-Dr. Salimuzzaman Siddiqui, Karachi, 75280, Pakistan 2. Department of Chemistry, University of Karachi, Karachi, 75270, Pakistan 3. H. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan 4. Interfakult?res Institut für Biochemie Der Universit?t Tübingen, Hoppe-Seyler-Stra?e 4, D-72076, Tübingen, Germany
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Abstract: | Thirteen (13) compounds of N-phenyl-O-alkyl carbamates (1 and 3), N,N-diethyl-N′-alkyl/aryl/phenylpiperazinoureas (4–6, 8–12), N-phenyl-N′-phenylpiperazino/imidazoureas (2, 7), and N-ethyl-(N′-phenylpiperazino) thioureas 13 were synthesized and tested for their antidepressant-like activity in mice. It was found that compound N-phenyl-O-heptyl carbamate 1 and N-phenyl-N′-phenylpiperazinourea 2 showed 32.5 and 27.7% antidepressant activity in the forced swim test in mice, respectively. Considering other carbamates it was found that a decrease in alkyl chain length caused a marked decline in the antidepressant activity. Compounds 1–4 show even higher activities in the forced swim test than the standard phenelzine. |
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