Yuhan Research Institute, 416-1, Gongse-dong, Giheung-gu, Yongin-si, Gyeonggi-do, Republic of Korea.
Bioorg Med Chem Lett. 2013 Jan 15;23(2):537-42. doi: 10.1016/j.bmcl.2012.11.018. Epub 2012 Nov 16.
Novel benzamide derivatives were synthesized and tested at in vitro assay by measuring fold increase of glucokinase activity at 5.0 mM glucose concentration. Among the prepared compounds, YH-GKA was found to be an active glucokinase activator with EC(50) of 70 nM. YH-GKA showed similar glucose AUC reduction of 29.6% (50 mg/kg) in an OGTT study with C57BL/J6 mice compared to 29.9% for metformin (300 mg/kg). Acute treatment of the compound in C57BL/J6 and ob/ob mice elicited basal glucose lowering activity. In subchronic study with ob/ob mice, YH-GKA showed significant decrease in blood glucose levels and no adverse effects on serum lipids or body weight. In addition, YH-GKA exhibited high bioavailability and moderate elimination in preclinical species.
新型苯甲酰胺衍生物被合成,并通过测量在 5.0mM 葡萄糖浓度下葡萄糖激酶活性的增加倍数来进行体外测定。在所制备的化合物中,YH-GKA 被发现是一种具有 EC(50)为 70nM 的有效的葡萄糖激酶激活剂。在 C57BL/J6 小鼠的 OGTT 研究中,YH-GKA 显示出与二甲双胍(300mg/kg)相似的葡萄糖 AUC 降低(29.6%,50mg/kg)。该化合物在 C57BL/J6 和 ob/ob 小鼠中的急性治疗引起了基础血糖降低活性。在 ob/ob 小鼠的亚慢性研究中,YH-GKA 显示出血糖水平的显著降低,对血清脂质或体重没有不良影响。此外,YH-GKA 在临床前物种中表现出高生物利用度和适度的消除。