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三德
Lv3
340 积分
2020-10-24 加入
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Discovery and optimization of novel pyrazole-benzimidazole CPL304110, as a potent and selective inhibitor of fibroblast growth factor receptors FGFR (1–3)
15天前
已完结
Discovery of a Selective and Orally Bioavailable FGFR2 Degrader for Treating Gastric Cancer
4个月前
已完结
Discovery of Potent and Selective WDR5 Proteolysis Targeting Chimeras as Potential Therapeutics for Pancreatic Cancer
4个月前
已完结
Discovery of highly efficient CRBN-recruiting HPK1-PROTAC as a potential chemical tool for investigation of scaffolding roles in TCR signaling
4个月前
已完结
Proteolysis-targeting chimeras with reduced off-targets
4个月前
已完结
Selective and Potent PROTAC Degraders of c-Src Kinase
4个月前
已完结
Design, synthesis, and evaluation of VHL-based EZH2 degraders for breast cancer
4个月前
已完结
Design, Synthesis, and Anticancer Evaluation of Arylurea Derivatives as Potent and Selective Type Ⅱ Irreversible Covalent FGFR4 Inhibitors
1年前
已完结
A first-in-human phase 1/2 study of FGF401 and combination of FGF401 with spartalizumab in patients with hepatocellular carcinoma or biomarker-selected solid tumors
1年前
已完结
The FGFR Landscape in Cancer: Analysis of 4,853 Tumors by Next-Generation Sequencing
1年前
已完结
没有进行任何应助
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1年前
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1年前
感谢,速度真快
1年前
感谢
1年前
感谢
1年前
速度真快,么么哒
1年前
感谢,速度真快
1年前
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