4.4 Article

Synthesis and Anticonvulsant Activity of 6-Alkoxy-[1,2,4]Triazolo[3,4-a]Phthalazines

期刊

CHEMICAL BIOLOGY & DRUG DESIGN
卷 73, 期 3, 页码 313-319

出版社

WILEY
DOI: 10.1111/j.1747-0285.2009.00776.x

关键词

anticonvulsant activity; synthesis; [1; 2; 4]triazolo[3; 4-a]-phthalazines

资金

  1. National Natural Science Foundation of China [30460151, 30760290]
  2. Important Item Foundation of Ministry of Education, PR China

向作者/读者索取更多资源

A new series of 6-alkoxy-[1,2,4]triazolo[3,4-a]phthalazines (3a-3v) were synthesized and their anticonvulsant activity and neurotoxicity were evaluated by the maximal electroshock test and the rotarod test respectively. Significant anticonvulsant activity was displayed by a number of compounds. The most promising compounds 6-(4-chlorobenzyloxy)-[1,2,4]triazolo[3,4-a]phthalazine (3f) and 6-heptyloxy-[1,2,4]triazolo[3,4-a]phthalazine (3s) showed a median effective dose of 7.1 and 11.0 mg/kg, and had protective index value of 5.2 and 8.0 respectively. The two compounds were further found to have potent activity against seizures induced by pentylenetetrazole, isoniazid, thiosemicarbazide, 3-mercaptopropionic acid but not seizures induced by strychnine, indicating that the two compounds might function by enhancing gamma-aminobutyric acid neurotransmission.

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