Skip to content
2000
Volume 10, Issue 8
  • ISSN: 1570-1808
  • E-ISSN: 1875-628X

Abstract

A series of new 2,5-disubstituted-1,3,4-oxadiazole derivatives 8(a-o) was synthesized by the reaction of 1-(5- phenyl-1,3,4-oxadiazol-2-yl)piperazine with various sulfonyl chlorides. The synthesized compounds were characterized by elemental analyses,1H NMR 13C NMR and mass spectral studies. The newly synthesized compounds were screened for their anticonvulsant activity against maximal electroshock (MES) seizure method and compared with the standard drug phenytoin. The neurotoxic effects were determined by rotorod test. Compounds 8d, 8e and 8f were found to be most potent of this series. The same compounds showed no neurotoxicity at the maximum dose administered (100 mg/kg). The efforts were also made to establish the structure activity relationships among synthesized compounds.

Loading

Article metrics loading...

/content/journals/lddd/10.2174/15701808113109990020
2013-10-01
2025-09-05
Loading full text...

Full text loading...

/content/journals/lddd/10.2174/15701808113109990020
Loading

  • Article Type:
    Research Article
Keyword(s): 1; 3; 4-oxadiazole; Anticonvulsant activity; Neurotoxicity; Rotorod; Synthesis
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test