作者:V. P. Chernykh、Zh. -P. Bulada、P. A. Bezuglyi、Yu. A. Golubenko、L. N. Voronina、A. I. Goncharov、V. A. Chubenko
DOI:10.1007/bf00758460
日期:1981.3
reported [i] the synthesis and biological activity of 1,3,5-thiadiazolyloxamicacidamides. We established that the hypoglycemic and antibacterial activity depend on the character of the substituents bonded to the amide nitrogen atom. It seemed of interest to obtain new derivatives of oxamic acid, viz., N-beteryloxamic acid hydrazones, and to investigate their biological activity. The synthesis of this group
我们之前曾报道过 [i] 1,3,5-噻二唑基肟酸酰胺的合成和生物活性。我们确定降血糖和抗菌活性取决于与酰胺氮原子键合的取代基的特征。获得草氨酸的新衍生物,即 N- 壬二酸腙,并研究它们的生物活性似乎很有趣。本组化合物的合成是通过该方案实现的