...
首页> 外文期刊>Bulletin of the Korean Chemical Society >Virtual Screening and Biochemical Evaluation of Mitogen-activated Protein Kinase Phosphatase 4 Inhibitors
【24h】

Virtual Screening and Biochemical Evaluation of Mitogen-activated Protein Kinase Phosphatase 4 Inhibitors

机译:丝裂原活化蛋白激酶磷酸酶4抑制剂的虚拟筛选和生化评估。

获取原文
获取原文并翻译 | 示例

摘要

Mitogen-activated protein kinase phosphatase 4 (MKP4) has proved to be a promising target for the development of therapeutics for the treatment of diabetes and the other metabolic diseases. Here, we report an example for a successful application of the structure-based virtual screening to identify three novel inhibitors of MKP4. These inhibitors have desirable physicochemical properties as a drug candidate and reveal a moderate potency with IC_(50) values ranging from 4.9 to 32.3 μM. Therefore, they deserve consideration for further development by structure-activity relationship studies to optimize the inhibitory and antidiabetic activities. Structural features relevant to the stabilization of the newly identified inhibitors in the active site of MKP4 are discussed in detail.
机译:丝裂原活化的蛋白激酶磷酸酶4(MKP4)已被证明是开发治疗糖尿病和其他代谢性疾病的疗法的有希望的目标。在这里,我们报告一个成功的应用实例,以基于结构的虚拟筛选来识别三种MKP4新型抑制剂。这些抑制剂作为候选药物具有理想的理化性质,并具有中等效力,IC_(50)值范围为4.9至32.3μM。因此,它们值得通过结构-活性关系研究来进一步开发以优化抑制和抗糖尿病活性。详细讨论了与新发现的抑制剂在MKP4活性位点的稳定化有关的结构特征。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号