Synthesis and studies on antidepressant and anticonvulsant activities of some 3-(2-furyl)-pyrazoline derivatives
Twelve 1-phenyl-, 1-thiocarbamoyl- and 1- N-substituted thiocarbamoyl-3-(2-furyl)-5-phenyl/(2-furyl)-2-pyrazoline derivatives were synthesized. The chemical structures of the compounds were proved by IR, 1H NMR, Mass spectrometric data and microanalyses. The antidepressant activities of the compound...
Saved in:
Published in: | European journal of medicinal chemistry Vol. 42; no. 3; pp. 373 - 379 |
---|---|
Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Oxford
Elsevier Masson SAS
01-03-2007
Elsevier |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Twelve 1-phenyl-, 1-thiocarbamoyl- and 1-
N-substituted thiocarbamoyl-3-(2-furyl)-5-phenyl/(2-furyl)-2-pyrazoline derivatives were synthesized. The chemical structures of the compounds were proved by IR,
1H NMR, Mass spectrometric data and microanalyses. The antidepressant activities of the compounds were investigated by Porsolt's behavioural despair (forced swimming) test on albino mice. 1-
N-Ethylthiocarbamoyl-3-(2-furyl)-5-phenyl-2-pyrazoline (
6) and 1-
N-allylthiocarbamoyl-3,5-di(2-furyl)-2-pyrazoline (
11) reduced 33.80–31.42% duration of immobility times at 10
mg
kg
−1 dose level. Anticonvulsant activities of the compounds were determined by maximal electroshock seizure (MES) and subcutaneous pentylenetetrazole (metrazol) (
scMet.) tests, neurotoxicities were determined by rotarod toxicity test on albino mice. 1,5-Diphenyl-3-(2-furyl)-2-pyrazoline (
2), 1-
N-allylthiocarbamoyl-3-(2-furyl)-5-phenyl-2-pyrazoline (
7), 1-
N-allylthiocarbamoyl-3,5-di(2-furyl)-2-pyrazoline (
11) and 1-
N-phenylthiocarbamoyl-3,5-di(2-furyl)-2-pyrazoline (
12) were active at 100–300
mg
kg
−1 dose levels. 1-Thiocarbamoyl-3,5-di(2-furyl)-2-pyrazoline (
4), 1-
N-methylthiocarbamoyl-3,5-di(2-furyl)-2-pyrazoline (
9) and 1-
N-ethylthiocarbamoyl-3,5-di(2-furyl)-2-pyrazoline (
10) were found protective against MES and
scMet. at 30–300
mg
kg
−1 dose levels.
[Display omitted] Several 3-(2-furyl)-2-pyrazoline derivatives were synthesized and evaluated for their antidepressant and anticonvulsant activities. Our pharmacological results indicate that they seem to be really promising compounds for their anticonvulsant activities. |
---|---|
ISSN: | 0223-5234 1768-3254 |
DOI: | 10.1016/j.ejmech.2006.09.006 |