哌啶
化学
类固醇
肾上腺素
孕烯醇酮
吡咯烷
效力
药理学
立体化学
内科学
体外
生物化学
医学
激素
作者
Otto Krayer,Frederick C. Uhle,Paula Ourisson
出处
期刊:PubMed
日期:1951-08-01
卷期号:102 (4): 261-8
被引量:1
摘要
Dihydroveratramine, tetrahydrojervine and Δ4-jervone, have been quantitatively compared with veratramine and jervine in regard to their antiaccelerator cardiac activity. The experiments were carried out using the heart-lung preparation of the dog under standard conditions of cardioacceleration caused by the continuous infusion of synthetic l -epinephrine.
A substance obtained by partial synthesis from pregnenolone, 20-(5'-methyl-2'-piperidyl)-Δ5-pregnen-3β, 20-diol, and kryptogenamine, prepared by partial synthesis from kryptogenin, have been shown to exhibit the characteristic antiaccelerator cardiac activity and have been included in the quantitative study.
The antiaccelerator cardiac activity decreases in the following order: veratramine > dihydroveratramine > tetrahydrojervine > 20-(5'-methyl-2'-piperidyl)-Δ5-pregnen-3β, 20-diol, jervine, Δ4-jervone > kryptogenamine.
Three types of steroid secondary amines exhibiting antiaccelerator cardiac activity, namely piperidine, pyrrolidine, and spiroaminoketal derivatives, have been considered. All of the substances characterized by high antiaccelerator potency are of the piperidine type.
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