【摘要】 以异嗪皮啶-3-甲酸为起始原料,通过与不同的氨类化合物缩合得异嗪皮啶-3-酰胺类化合物,从而得到了一类新的异嗪皮啶-3-酰胺化合物,并对其进行了抗肿瘤活性研究。目标化合物结构经MS、~1H NMR确证。更多还原

【Abstract】 Using isofraxidin-3-formic acid as the starting material, condensating with different amines, a series of novel isofraxidin-3-amide compounds were obtained. The antitumor activities of these isofraxidin-3-formic compounds were also evaluated. The structure of the target compound was confirmed by MS and ~1 H NMR.更多还原