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...
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Published in: | European journal of medicinal chemistry Vol. 42; no. 3; pp. 373 - 379 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
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Elsevier Masson SAS
01-03-2007
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Abstract | 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. |
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AbstractList | 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. 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, (1)H 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. |
Author | Bilgin, A. Altan Özdemir, Zuhal Kandilci, H. Burak Gümüşel, Bülent Çalış, Ünsal |
Author_xml | – sequence: 1 givenname: Zuhal surname: Özdemir fullname: Özdemir, Zuhal organization: Hacettepe University Faculty of Pharmacy, Department of Pharmaceutical Chemistry, 06100 Ankara, Turkey – sequence: 2 givenname: H. Burak surname: Kandilci fullname: Kandilci, H. Burak organization: Hacettepe University Faculty of Pharmacy, Department of Pharmacology, 06100 Ankara, Turkey – sequence: 3 givenname: Bülent surname: Gümüşel fullname: Gümüşel, Bülent organization: Hacettepe University Faculty of Pharmacy, Department of Pharmacology, 06100 Ankara, Turkey – sequence: 4 givenname: Ünsal surname: Çalış fullname: Çalış, Ünsal organization: Hacettepe University Faculty of Pharmacy, Department of Pharmaceutical Chemistry, 06100 Ankara, Turkey – sequence: 5 givenname: A. Altan surname: Bilgin fullname: Bilgin, A. Altan email: abilgin@hacettepe.edu.tr organization: Hacettepe University Faculty of Pharmacy, Department of Pharmaceutical Chemistry, 06100 Ankara, Turkey |
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ContentType | Journal Article |
Copyright | 2006 Elsevier Masson SAS 2007 INIST-CNRS |
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Keywords | Thiocarbamoyl compounds Anticonvulsant activity Antidepressant activity Pyrazolines Psychotropic Toxicity Rodentia Furan derivatives Nervous system Anticonvulsant Biological activity Vertebrata Neurotoxicity Mammalia Mouse Animal Pyrazole derivatives Antidepressant agent Chemical synthesis |
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Snippet | Twelve 1-phenyl-, 1-thiocarbamoyl- and 1-
N-substituted thiocarbamoyl-3-(2-furyl)-5-phenyl/(2-furyl)-2-pyrazoline derivatives were synthesized. The chemical... Twelve 1-phenyl-, 1-thiocarbamoyl- and 1-N-substituted thiocarbamoyl-3-(2-furyl)-5-phenyl/(2-furyl)-2-pyrazoline derivatives were synthesized. The chemical... |
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SubjectTerms | Animals Anticonvulsant activity Anticonvulsants - chemical synthesis Anticonvulsants - pharmacology Anticonvulsants - toxicity Anticonvulsants. Antiepileptics. Antiparkinson agents Antidepressant activity Antidepressive Agents - chemical synthesis Antidepressive Agents - pharmacology Antidepressive Agents - toxicity Biological and medical sciences Convulsants Electroshock Furans - chemical synthesis Furans - pharmacology Magnetic Resonance Spectroscopy Male Medical sciences Mice Neuropharmacology Neurotoxicity Syndromes - psychology Pentylenetetrazole Pharmacology. Drug treatments Postural Balance - drug effects Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) Psychology. Psychoanalysis. Psychiatry Psychopharmacology Pyrazoles - chemical synthesis Pyrazoles - pharmacology Pyrazolines Seizures - chemically induced Seizures - drug therapy Spectrophotometry, Ultraviolet Structure-Activity Relationship Swimming - psychology Thiocarbamoyl compounds |
Title | Synthesis and studies on antidepressant and anticonvulsant activities of some 3-(2-furyl)-pyrazoline derivatives |
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