Cardiovascular, Metabolic & Endocrine Diseases Chemistry, Pfizer Worldwide Research & Development , 610 Main St, Cambridge, MA 02139 , USA +1 617 551 3267 ; +1 617 551 3082 ;
Expert Opin Ther Pat. 2014 Aug;24(8):875-91. doi: 10.1517/13543776.2014.918957. Epub 2014 May 12.
Glucokinase (GK) is a key regulator of glucose homeostasis, and development of small molecule activators of this enzyme represents a promising new approach for the treatment of type 2 diabetes mellitus.
This manuscript reviews small molecule patent disclosures between late 2011 and February 2014 for both GK activators (GKAs) and GK-glucokinase regulatory protein (GK-GKRP) disruptors. The review is organized by company and structural class.
The field of GKA research continues to progress, driven by research across many organizations. To date, > 20 candidates have entered clinical development with the most advanced in Phase II trials. Despite promising efficacy, a significant number of early candidates have been discontinued for various reasons including increased risk of hypoglycemia and lack of durability. Recent work in the field has focused on liver-selective activators, which have shown lower hypoglycemia risk, including the development of novel GK-GKRP disruptors that act to indirectly increase hepatic GK activity.
葡萄糖激酶(GK)是葡萄糖稳态的关键调节剂,开发这种酶的小分子激活剂代表了治疗 2 型糖尿病的一种很有前途的新方法。
本文综述了 2011 年末至 2014 年 2 月期间,GK 激活剂(GKAs)和 GK-葡萄糖激酶调节蛋白(GK-GKRP)抑制剂的小分子专利公开情况。综述按公司和结构类别进行组织。
由于许多组织的研究,GKAs 的研究领域不断取得进展。迄今为止,已有超过 20 个候选药物进入临床开发阶段,其中最先进的候选药物处于 II 期试验阶段。尽管疗效有希望,但由于包括低血糖风险增加和耐久性缺乏在内的各种原因,许多早期候选药物已被停止开发。该领域的最新研究集中在肝选择性激活剂上,这些激活剂显示出低血糖风险较低,包括开发新型 GK-GKRP 抑制剂,这些抑制剂可间接增加肝 GK 活性。