PARP1
化学
药理学
IC50型
聚ADP核糖聚合酶
伊立替康
体外
癌症
癌症研究
酶
生物化学
生物
医学
内科学
聚合酶
结直肠癌
作者
Tao Guo,Yongting Yuan,Ziyan Ma,Yurong Zou,Minghai Tang,Zhongning Guo,Zhiyuan Fu,Weichen Bo,Peng Wang,Shuai Liu,Hao Huang,Junfeng Hu,Zhuang Yang,Tao Jia,Taijin Wang,Lijuan Chen
标识
DOI:10.1021/acs.jmedchem.5c00185
摘要
inhibited tumor growth in the BRCA mutant MDA-MB-436 xenograft model and showed synergistic efficacy in combination with irinotecan in the HCT116 xenograft model, suggesting that it could be a promising candidate drug combined with chemotherapy for the treatment of cancer. These findings indicate that the strategy proposed in this study is highly significant for the development of selective PARP1 inhibitors.
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