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

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Abstract

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. © 2009 Blackwell Munksgaard.

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APA

Zhang, L., Guan, L. P., Sun, X. Y., Wei, C. X., Chai, K. Y., & Quan, Z. S. (2009). Synthesis and anticonvulsant activity of 6-Alkoxy-[1,2,4]Triazolo[3,4-a] Phthalazines. Chemical Biology and Drug Design, 73(3), 313–319. https://doi.org/10.1111/j.1747-0285.2009.00776.x

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