A series of new pyridazinylacetic acid derivatives were synthesized and have been investigated for their ability to inhibit the activity of the A and B isoforms of monoamine oxidase (MAO). All compounds were found to be more selective to the MAO-A isoform with compound 5d having the highest SI values. Computational study performed with a docking technique indicated the potential of these compounds in pyridazine-based MAO-A inhibitor drug development.
我们合成了一系列新的
哒嗪基
乙酸衍
生物,并研究了它们抑制单胺氧化酶(MAO)A 和 B 同工酶活性的能力。研究发现,所有化合物都对 MAO-A 异构体具有更高的选择性,其中化合物 5d 的 SI 值最高。利用对接技术进行的计算研究表明,这些化合物具有开发基于
哒嗪的 MAO-A
抑制剂药物的潜力。