Lv42
680 积分 2022-12-05 加入
Computational insights into allosteric inhibition of focal adhesion kinase: A combined pharmacophore modeling and molecular dynamics approach
5天前
已完结
Discovery of novel pyrrolo [2,3-d] pyrimidine derivatives as potent FAK inhibitors based on cyclization strategy
5天前
已完结
DNA damage response inhibitors in cancer therapy: lessons from the past, current status and future implications
17天前
已完结
Targeting DNA damage response pathways in cancer
17天前
已完结
CDK2 heterobifunctional degraders co-degrade CDK2 and cyclin E resulting in efficacy in CCNE1-amplified and overexpressed cancers
18天前
已完结
CDK2 heterobifunctional degraders co-degrade CDK2 and cyclin E resulting in efficacy in CCNE1-amplified and overexpressed cancers
18天前
已完结
Discovery of AZD8421: A Potent CDK2 Inhibitor with Selectivity Against Other CDK Family Members and the Human Kinome
19天前
已完结
SARM1 activation promotes axonal degeneration via a two-step phase transition
19天前
已完结
Expression of CD38 in human neuroblastoma SH-SY5Y cells
1个月前
已完结
A novel FAK-degrading PROTAC molecule exhibited both anti-tumor activities and efficient MDR reversal effects
1个月前
已完结
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