前药
化学
抗惊厥药
苯妥英钠
药品
药理学
口服
羟甲基
溶解度
加药
立体化学
有机化学
生物化学
医学
癫痫
精神科
作者
Sailesh A. Varia,S. Schuller,Kenneth B. Sloan,Valentino J. Stella
标识
DOI:10.1002/jps.2600730812
摘要
Various bioreversible derivatives of phenytoin, a poorly water soluble and erratically absorbed drug after both oral and parenteral dosing, were synthesized. Initial evaluation of these expected prodrugs, i.e., their aqueous solubility, cleavage in the presence of various animal tissues, and anticonvulsant activity in mice, confirmed that a number of the derivatives did indeed behave as prodrugs. The more promising prodrugs were the disodium phosphate ester and various amino groups containing acyl esters of 3-(hydroxymethyl)-5,5-diphenylhydantoin.
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