EN
×
EN
在线咨询
在线
咨询
电话
电话
微信公众号
业务咨询
中国:
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)
留言
留言
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9728太阳集团首页进行

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
Baidu
sogou