Department of Organic and Physical Chemistry, Faculty of Pharmacy, Medical University of Warsaw, 1 Banacha Str., 02-097 Warsaw, Poland.
Centre for Preclinical Research and Technology, Department of Pharmacodynamics, Faculty of Pharmacy, Medical University of Warsaw, 1 Banacha Str., 02-097 Warsaw, Poland.
Int J Mol Sci. 2023 Feb 1;24(3):2779. doi: 10.3390/ijms24032779.
A series of 15 new derivatives of 6-acetyl-7-hydroxy-4-methylcoumarin containing a piperazine group were designed with the help of computational methods and were synthesized to study their affinity for the serotonin 5-HT and 5-HT receptors. Among them, 6-acetyl-7-{4-[4-(3-bromophenyl)piperazin-1-yl]butoxy}-4-methylchromen-2-one () and 6-acetyl-7-{4-[4-(2-chlorophenyl)piperazin-1-yl]butoxy}-4-methylchromen-2-one () exhibited excellent activity for 5-HT receptors with Ki values 0.78 (0.4-1.4) nM and 0.57 (0.2-1.3) nM, respectively, comparable to the Ki values of 8-OH-DPAT (0.25 (0.097-0.66) nM). The equilibrium dissociation constant values of the tested compounds showed differential intrinsic activities of the agonist and antagonist modes.
一系列含有哌嗪基团的 6-乙酰基-7-羟基-4-甲基香豆素的 15 个新衍生物在计算方法的帮助下被设计出来,并被合成以研究它们对 5-羟色胺 5-HT 和 5-HT 受体的亲和力。其中,6-乙酰基-7-{4-[4-(3-溴苯基)哌嗪-1-基]丁氧基}-4-甲基色烯-2-酮()和 6-乙酰基-7-{4-[4-(2-氯苯基)哌嗪-1-基]丁氧基}-4-甲基色烯-2-酮()对 5-HT 受体表现出优异的活性,Ki 值分别为 0.78(0.4-1.4)nM 和 0.57(0.2-1.3)nM,与 8-OH-DPAT(Ki 值为 0.25(0.097-0.66)nM)相当。测试化合物的平衡解离常数值显示出激动剂和拮抗剂模式的不同内在活性。