Vesicular monoamine transporter type 2 (VMAT2) is a newly emerging target for both diagnostic and therapeutic applications in diabetes mellitus. In pursuit of novel VMAT2 antagonists, we identified a potent hypoglycemic agent with a novel dihydropyridone scaffold. Several analogs were designed and synthesized. A preliminary structure activity relationship (SAR) showed that the dihydropyridone scaffold
囊泡单胺转运蛋白 2 型 (VMAT2) 是糖尿病诊断和治疗应用的新兴靶点。为了寻找新型 VMAT2 拮抗剂,我们确定了一种具有新型
二氢吡啶酮支架的强效降血糖药。设计并合成了几种类似物。初步的构效关系 (
SAR) 表明该活性需要
二氢吡啶酮支架。