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KMID : 0370219830270040289
Yakhak Hoeji
1983 Volume.27 No. 4 p.289 ~ p.293
Syntheses and Central Nervous Depressant Activity of Piperine Derivatives(III) N-Piperoyl Amino Acids
ÀÌÇѱ¸/Lee HK
ÀÓÁß±â/ÀÌÀº¹æ/¿ì¿ø½Ä/Lim JK/Lee EB/Woo WS
Abstract
Twelve new N-piperoyl amino acids were synthesized by acylation of amino acids with piperoylchloride in order to develop the new central nervous depressants. Silylation of the carboxylic group of amino acids not only precluded side reactions but also facilitated acylation at room temperature without catalysts. The acute toxicity of all the synthesized compounds were lower than that of piperine itself, whereas they showed strong protective effect against the strychnine-induced mortality.
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