Signalchem Lifesciences Corp. , 550-5600 Parkwood Way, Richmond, British Columbia, V6V 2M2, Canada.
J Med Chem. 2014 Jun 26;57(12):5039-56. doi: 10.1021/jm401516c. Epub 2013 Dec 20.
This review provides an overview of stearoyl-coenzyme A desaturase-1 (SCD1) as a novel therapeutic target for metabolic disorders and other indications. Target validation is reviewed, and limitations due to incomplete knowledge of the relevant biological systems are described. Assay development, particularly for high throughput screening, and characterization of SCD1 inhibition are summarized. The progress and evolution in medicinal chemistry are discussed, specifically focusing on key attributes of the most advanced SCD1 inhibitors described in the primary literature and in patent applications. This work culminated in numerous companies identifying potent selective inhibitors, some of which progressed to early clinical development. The status of current SCD1 drug discovery programs is reviewed. Challenges are discussed, and potential new directions are indicated.
这篇综述概述了硬脂酰辅酶 A 去饱和酶-1(SCD1)作为代谢紊乱和其他适应症的新型治疗靶点。综述了靶标验证,并描述了由于对相关生物系统了解不完整而产生的局限性。总结了测定法的发展,特别是高通量筛选和 SCD1 抑制作用的特性。讨论了药物化学的进展和演变,特别是重点介绍了主要文献和专利申请中描述的最先进的 SCD1 抑制剂的关键属性。这项工作最终导致许多公司确定了有效的选择性抑制剂,其中一些已进入早期临床开发阶段。综述了当前 SCD1 药物发现计划的现状。讨论了挑战,并指出了潜在的新方向。