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强心甾内酯类似物。对AY 22241常见性质的解释。

Cardenolide analogs. An explanation for the usual properties of AY 22241.

作者信息

Thomas R, Allen J, Pitts B J, Schwartz A

出版信息

Eur J Pharmacol. 1979 Jan 15;53(3):227-37. doi: 10.1016/0014-2999(79)90128-6.

Abstract

AY 22241 (AY) was compared with digitoxigenin with respect to effects on myocardial contractility and inhibition of Na+, K+-ATPase. Ay was less potent than digitoxigenin but otherwise showed the same type of rapid onset and rapid reversal of activity usually associated with genins. Since AY is a glycoside, its behaviour was regarded as anomalous since glycosides usually show both slow onset and slow reversal of activity. Attempts were made to account for the genin-like properties of AY in terms of the model for the digitalis receptor proposed by Thomas et al. (1974a,b). It is suggested that the low potency and genin-like properties of AY may be due to the fact that the steroid is attached to the lactone through the carbon atom that is alpha to the carbonyl group. This feature could result in non-alignment of the sugar residue with the sugar binding site and might also reduce the effectiveness of the interaction of the steroid moiety with its binding site. A notable feature of AY toxicity was its extremely rapid progression to irreversible fibrillation.

摘要

将AY 22241(AY)与洋地黄毒苷配基在对心肌收缩力的影响以及对Na +,K + -ATP酶的抑制作用方面进行了比较。AY的效力低于洋地黄毒苷配基,但在其他方面表现出与通常与配基相关的相同类型的起效迅速和活性快速逆转。由于AY是一种糖苷,其行为被认为是异常的,因为糖苷通常表现出起效缓慢和活性逆转缓慢。人们试图根据Thomas等人(1974a,b)提出的洋地黄受体模型来解释AY的配基样性质。有人提出,AY的低效和配基样性质可能是由于甾体通过与羰基相邻的碳原子连接到内酯上。这一特征可能导致糖残基与糖结合位点不对齐,也可能降低甾体部分与其结合位点相互作用的有效性。AY毒性的一个显著特征是其极其迅速地发展为不可逆的颤动。

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