Synthesis and Anti-Arrhythmic Activity of the Chloride and Salicylate Salts of Morpholinoacetic Acid Ortho-Toluidide
作者:O. V. Gashkova、I. P. Rudakova、B. Ya. Syropyatov
DOI:10.1007/s11094-017-1667-3
日期:2017.11
amination by morpholine in the presence of an excess of Et3N produced morpholinoacetic acid ortho-toluidide and its salicylate salt. The acute toxicity and anti-arrhythmic and antifibrillatory activities of these compounds were studied. The biological activities indicated that these compounds were promising for further studies and evaluation of their potential for implementation into medical practice.
用氯乙酰氯酰化邻甲苯胺盐酸盐,然后在过量 Et3N 存在下用吗啉胺化,生成吗啉乙酸邻甲苯胺及其水杨酸盐。研究了这些化合物的急性毒性和抗心律失常和抗纤颤活性。生物活性表明,这些化合物有望用于进一步研究和评估其在医疗实践中的应用潜力。