在实验室条件下对已改性基酸衍生物在老鼠心血管功能的基本药理学评估

Eva Kralova1, Ivan Malik2

  • 1Department of Pharmacology and Toxicology, Faculty of Pharmacy, Comenius University, Bratislava, Slovakia.

PubMed
概括

新的甲酸衍生物在老鼠身上进行了测试. 化合物表现出β-阻断剂和α-上腺溶解性质,其中化合物6d对血管收缩最有效,6c对心率增加最有效.

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