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
Main Authors: Özdemir, Zuhal, Kandilci, H. Burak, Gümüşel, Bülent, Çalış, Ünsal, Bilgin, A. Altan
Format: Journal Article
Language:English
Published: Oxford Elsevier Masson SAS 01-03-2007
Elsevier
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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.
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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Issue 3
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
Language English
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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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StartPage 373
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
URI https://dx.doi.org/10.1016/j.ejmech.2006.09.006
https://www.ncbi.nlm.nih.gov/pubmed/17069933
Volume 42
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