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双-β-羟丙基丙二酸二内酯衍生物的药理特性

Pharmacological properties of bis-beta-hydroxypropylmalonic acid dilactone derivatives.

作者信息

Sypniewska M

出版信息

Pol J Pharmacol Pharm. 1976;28(2):157-65.

PMID:945562
Abstract

Acute toxicity and the action on CNS (employing behavioural tests) of bis-beta-hydroxypropylmalonic acid dilactone (D1) and its four derivatives (D2--D5) were investigated (Table 1) in mice and rats. The studied compounds showed low toxicity and were sometimes active just from high doses. D1 can be regarded as a sedative--hypnotic compound. In animals, the substituted dilactones induced the symptoms similar to those of tranquilizers.

摘要

在小鼠和大鼠中研究了双-β-羟丙基丙二酸二内酯(D1)及其四种衍生物(D2 - D5)的急性毒性以及对中枢神经系统的作用(采用行为测试)(表1)。所研究的化合物显示出低毒性,有时仅在高剂量时才有活性。D1可被视为一种镇静催眠化合物。在动物中,取代的二内酯诱导出与镇静剂类似的症状。

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