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Some new 2-aryloxymethyl-3-alpha-substituted carboxymethyl-6,8-substituted-4-quinazolones as possible anticonvulsants.

作者信息

Husain M I, Singh E

出版信息

Pharmazie. 1982 Jun;37(6):408-10. doi: 10.1002/chin.198245247.

Abstract

In view of their expected MAO inhibitory, CNS depressant and anticonvulsant properties, thirty new 2-aryloxymethyl-3-alpha-substituted carboxymethyl-6,8-substituted-4-quinazolones were synthesized by the reaction of substituted anthranil with various amino acids in pyridine. Some of these compounds at a concentration of 1 X 10(-3) mol/l inhibited rat brain monamine oxidase (MAO) in vitro and provided protection against pentylenetetrazole induced convulsions in mice.

摘要

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Monoamine oxidase inhibitory and CNS activities of some quinazolinones.
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