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[3-甲基-6-或-8-氮杂喹喔啉-2(1H)酮的叔氨基烷基衍生物。对大鼠条件性回避反应获得和改变的影响]

[Tertiary aminoalkyl derivatives of 3-methyl-6- or -8-azaquinoxalin-2(1H)ones. Effect on acquisition and modification of a conditioned avoidance response in rats].

作者信息

Pirisino G, Alamanni M C, Savelli F, Sparatore F, Manca P, Satta M

出版信息

Farmaco Sci. 1983 May;38(5):330-9.

PMID:6862003
Abstract

Eight derivatives of 3-methyl-6-azaquinoxalin-2(1H)-one and of 3-methyl-8-azaquinoxalin-2(1H)-one were prepared. They bear on position 1 an aminoalkyl chain (dimethylaminoethyl, morpholinylethyl, dimethylaminopropyl and N-methylpiperazinylpropyl). Three of these compounds exhibit a high degree of deconditioning activity on rats; compound (I) is particularly active on the acquisition of a conditioned avoidance response, while compound (II) is more active than chloropromazine on the modification of a C.A.R. Compound (II) is characterized also by low toxicity.

摘要

制备了3-甲基-6-氮杂喹喔啉-2(1H)-酮和3-甲基-8-氮杂喹喔啉-2(1H)-酮的八种衍生物。它们在1位带有一个氨基烷基链(二甲基氨基乙基、吗啉基乙基、二甲基氨基丙基和N-甲基哌嗪基丙基)。其中三种化合物对大鼠表现出高度的去条件化活性;化合物(I)对条件性回避反应的习得特别有效,而化合物(II)在改变条件性回避反应方面比氯丙嗪更有效。化合物(II)还具有低毒性的特点。

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