We have identified SRT2104 (4) as the first direct synthetic SIRT1 activator clinical candidate. The compound
was derived from the optimization of a previously described imidazo[1,2-b]thiazole scaffold. SRT2104 was selected as a
development candidate based on a combination of biochemical activity and pharmacokinetic profile. The in vivo characteristics
of SRT2104 were superior to those of analogues with similar activation profiles. The overall preclinical profile
suggests that the compound has potential to provide therapeutic benefit in a clinical setting.
我们发现 SRT2104 (4) 是首个直接合成的 SIRT1 激活剂临床候选药物。该化合物是通过优化之前描述的
咪唑并[1,2-b]
噻唑支架而得到的。SRT2104 是基于生化活性和药代动力学特征的综合考虑而被选为候选开发药物的。SRT2104 的体内特性优于具有类似活化特征的类似物。整体临床前研究结果表明,该化合物具有在临床环境中提供治疗益处的潜力。