Jung Jae-Kyu, Johnson Benjamin R, Duong Tracy, Decaire Marc, Uy Jane, Gharbaoui Tawfik, Boatman P Douglas, Sage Carleton R, Chen Ruoping, Richman Jeremy G, Connolly Daniel T, Semple Graeme
Department of Medicinal Chemistry, Arena Pharmaceuticals, 6166 Nancy Ridge Drive, San Diego, California 92121, USA.
J Med Chem. 2007 Apr 5;50(7):1445-8. doi: 10.1021/jm070022x. Epub 2007 Mar 15.
Recently identified GPCRs, GPR109a and GPR109b, the high and low affinity receptors for niacin, may represent good targets for the development of HDL elevating drugs for the treatment of atherosclerosis. Acifran, an agonist of both receptors, has been tested in human subjects, yet until recently very few analogs had been reported. We describe a series of acifran analogs prepared using newly developed synthetic pathways and evaluated as agonists for GPR109a and GPR109b, resulting in identification of compounds with improved activity at these receptors.
最近发现的G蛋白偶联受体(GPCRs)GPR109a和GPR109b是烟酸的高亲和力和低亲和力受体,它们可能是开发用于治疗动脉粥样硬化的高密度脂蛋白(HDL)升高药物的良好靶点。阿西夫兰是这两种受体的激动剂,已在人体受试者中进行了测试,但直到最近,报道的类似物还很少。我们描述了一系列使用新开发的合成途径制备的阿西夫兰类似物,并将其评估为GPR109a和GPR109b的激动剂,从而鉴定出在这些受体上具有改善活性的化合物。