邵国贤, 贺文义, 华毅. 儿茶氨基酮及类似物的合成J. 药学学报, 1990, 25(2): 101-109.
引用本文: 邵国贤, 贺文义, 华毅. 儿茶氨基酮及类似物的合成J. 药学学报, 1990, 25(2): 101-109.
GX Shao WY He, Y Hua, . SYNTHESIS OF CATECHOL AMINOKETONE AND ITS ANALOGUESJ. Acta Pharmaceutica Sinica, 1990, 25(2): 101-109.
Citation: GX Shao WY He, Y Hua, . SYNTHESIS OF CATECHOL AMINOKETONE AND ITS ANALOGUESJ. Acta Pharmaceutica Sinica, 1990, 25(2): 101-109.

儿茶氨基酮及类似物的合成

SYNTHESIS OF CATECHOL AMINOKETONE AND ITS ANALOGUES

  • 摘要: 本文报道儿茶氨基酮Ⅰ1~12及类似物Ⅱ1~12共24个和一个尿嘧啶氨基酮Ⅲ的合成。并对上述化合物的核磁共振谱及质谱进行了讨论。药理研究表明这类化合物对5-HT和Ca#引起的离体犬肠系膜动脉和基底动脉的收缩无明显对抗作用。某些化合物能增加在体犬股动脉血流量,显示其扩血管作用。其中以Ⅰ10作用最明显,静脉注射后有轻度的降压反应,并能增加麻醉犬的冠状动脉血流量和心肌收缩力,对乌头碱及氯仿诱导的心律失常亦有保护作用。

     

    Abstract: In this paper, the synthesis of a series of aminoketone derivatives are reported.Compounds Ⅰ1~9 and Ⅱ1~10 were synthesized from substituted chloroacetophenone with various amines. Compounds Ⅰ10~12 and Ⅱ11~12 were synthesized from substituted acetophenones with corresponding amines through Mannich reaction. The 1HNMR and MS were discussed. Pharmacological study showed that the vascular contraction of dog ruesenteric and basilar arteries induced by serotonine and calcium in vitro could not be antagonized by this kind of compounds and the known compound 3,4-dihydroxy acetophenone (Ⅰ0) Except Ⅰ10, the vasodilator effects of all compounds as shown by measurement of arterial blood flow after injection into femoral artery in dogs are weaker than Ⅰ0. After intravenous injection in anesthetized dogs, Ⅰ10 showed the same effect as Ⅰ0 to increase coronary blood flow and myocardial contraction. Furthermore, the ventricular arrhythmia induced by aconitine and chloroform could also be protected by compound Ⅰ10, but compound Ⅰ0 was not effective.

     

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