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1-(4-((3-(4-甲基哌嗪-1-基)丙基)氨基)苄基)-5-(三氟甲基)吡啶-2(1H)-酮的发现,一种用于治疗糖尿病肾病的口服活性多靶点药物。

Discovery of 1-(4-((3-(4-methylpiperazin-1-yl)propyl)amino)benzyl)-5-(trifluoromethyl)pyridin-2(1H)-one, an orally active multi-target agent for the treatment of diabetic nephropathy.

作者信息

Chen Jun, Peng Zhangzhe, Lu Miaomiao, Xiong Xuan, Chen Zhuo, Li Qianbin, Cheng Zeneng, Jiang Dejian, Tao Lijian, Hu Gaoyun

机构信息

Department of Medicinal Chemistry, Xiangya School of Pharmacy, Central South University, Changsha 410013, China.

Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008, China.

出版信息

Bioorg Med Chem Lett. 2018 Jan 15;28(2):222-229. doi: 10.1016/j.bmcl.2017.07.001. Epub 2017 Jul 4.

Abstract

Oxidative stress, inflammation and fibrosis can cause irreversible damage on cell structure and function of kidney and are key pathological factors in Diabetic Nephropathy (DN). Therefore, multi-target agents are urgently need for the clinical treatment of DN. Using Pirfenidone as a lead compound and based on the previous research, two novel series (5-trifluoromethyl)-2(1H)-pyridone analogs were designed and synthesized. SAR of (5-trifluoromethyl)-2(1H)-pyridone derivatives containing nitrogen heterocyclic ring have been established for in vitro potency. In addition, compound 8, a novel agent that act on multiple targets of anti-DN with IC of 90μM in NIH3T3 cell lines, t of 4.89±1.33h in male rats and LD>2000mg/kg in mice, has been advanced to preclinical studies as an oral treatment for DN.

摘要

氧化应激、炎症和纤维化可对肾脏的细胞结构和功能造成不可逆损伤,是糖尿病肾病(DN)的关键病理因素。因此,临床上迫切需要用于治疗DN的多靶点药物。以吡非尼酮为先导化合物,基于前期研究,设计并合成了两个新型系列的(5-三氟甲基)-2(1H)-吡啶酮类似物。已建立含氮杂环的(5-三氟甲基)-2(1H)-吡啶酮衍生物的体外活性构效关系。此外,化合物8作为一种作用于DN多个靶点的新型药物,在NIH3T3细胞系中的IC为90μM,在雄性大鼠中的t为4.89±1.33小时,在小鼠中的LD>2000mg/kg,已作为DN的口服治疗药物进入临床前研究阶段。

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