Acyl derivatives of phenothiazine and their dibenzazepine analogs: Structure and antiarrhythmic activity
作者:S. Yu. Berdyaev、A. I. Turilova、Z. P. Senova、A. N. Gritsenko、N. V. Kaverina、A. P. Skoldinov
DOI:10.1007/bf00766356
日期:1991.1
original highly effective antiarrhythmic agents, ethmosine, and ethacizine [2, 3, 5-8], which have been evaluated highly by clinicians in the USSR and abroad [9-11, 15, 16]. The correlations between chemical structure and antiarrhythmic activity revealed for the example of these phenothiazine derivatives have permitted the discovery of compounds with promising antiarrhythmic properties among the corresponding
苏联医学科学院药理学研究所的化学家和药理学家在吩噻嗪的二烷基氨基酰基衍生物系列中的系统工作以发现独创的高效抗心律失常药乙胺嘧啶和乙西嗪而告终[2, 3, 5- 8],得到了苏联和国外临床医生的高度评价 [9-11, 15, 16]。以这些吩噻嗪衍生物为例,揭示的化学结构与抗心律失常活性之间的相关性允许在相应类似构建的二苯并氮杂氨基酰基衍生物中发现具有良好抗心律失常特性的化合物,代表与吩噻嗪相关的三环含氮系统。Bonnecor 具有原始的抗心律失常作用谱 [12-14, 17],