pg电子官网

      EN
      ×
      EN
      • 业务咨询

        中国:

        Email: marketing@shtongxi.com.cn

        业务咨询专线:400-780-8018

        (仅限服务咨询,其他事宜请拨打川沙总部电话)

        川沙总部电话: +86 (21) 5859-1500

        海外:

        +1(781)535-1428(U.S.)

        0044 7790 816 954 (Europe)

        Email:marketing@medicilon.com

      在线留言×
      点击切换
      Customer Center
      客户中心

      研究人员设计合成STAT3和HDAC双通路抑制剂用于治疗实体肿瘤,PK实验通过pg电子官网进行

      2023-07-05
      |
      访问量:

      56.png

      The inhibition of HDACs will lead to compensated activation of a notorious cancer-related drug target, STAT3, in breast cancer through a cascade, which probably limits the anti-proliferation effect of HDAC inhibitors in solid tumors. 

      Herein, researchers synthesized a series of potent pterostilbene hydroxamic acid derivatives with dual-target inhibition activity. 

      The pharmacokinetic experiment in SD Rats was carried out by Medicilon.

      Reference:

      Yuhao Ren, et al. Discovery of STAT3 and Histone Deacetylase (HDAC) Dual-Pathway Inhibitors for the Treatment of Solid Cancer. J Med Chem. 2021 Jun 10;64(11):7468-7482. doi: 10.1021/acs.jmedchem.1c00136. 

      相关新闻
      ×
      搜索验证
      点击切换
      友情链接: