State Key Laboratory of Natural Medicines, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing 210009, PR China; Department of Organic Chemistry, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing 210009, PR China.
Bioorg Med Chem. 2013 Dec 15;21(24):7742-51. doi: 10.1016/j.bmc.2013.10.017. Epub 2013 Oct 23.
A series of novel 1,2,4-triazole bearing 5-substituted biphenyl-2-sulfonamide derivatives were designed and synthesized to develop new angiotensin II subtype 2 (AT2) receptor agonists as novel antihypertensive candidates. It was found that 14f (IC50=0.4 nM) and 15e (IC50=5.0 nM) displayed potent AT2 receptor affinity and selectivity in binding assays. Biological evaluation in vivo suggested that 14f is obviously superior to that of reference drug losartan in RHRs, and meanwhile, 14f has no significant impact on heart rate. The interesting activities of these compounds may make them promising candidates as antihypertensive agents.
设计并合成了一系列新型含 1,2,4-三唑基的 5-取代联苯-2-磺酰胺衍生物,以期开发新型血管紧张素 II 亚型 2(AT2)受体激动剂作为新型抗高血压候选药物。研究发现,化合物 14f(IC50=0.4 nM)和 15e(IC50=5.0 nM)在结合实验中表现出对 AT2 受体的高亲和性和选择性。体内生物学评价表明,化合物 14f 在 RHRs 中的活性明显优于阳性对照药氯沙坦,同时,14f 对心率没有显著影响。这些化合物的有趣活性可能使它们成为有前途的抗高血压药物候选物。