Lv6
1709 积分 2024-03-21 加入
Crystal Structure of the Human Cell Cycle Protein CksHs1: Single Domain Fold with Similarity to Kinase N-lobe Domain
20天前
已完结
Design, Synthesis, and Biological Evaluation of Aminoindazole Derivatives as Highly Selective Covalent Inhibitors of Wild-Type and Gatekeeper Mutant FGFR4
1个月前
已完结
Design, Synthesis, and Biological Evaluation of 5-Formyl-pyrrolo[3,2-b]pyridine-3-carboxamides as New Selective, Potent, and Reversible-Covalent FGFR4 Inhibitors
1个月前
已完结
Optimization of Aminoindazole derivatives as highly selective covalent inhibitors for wild-type and mutant FGFR4
1个月前
已完结
Optimization of Aminoindazole derivatives as highly selective covalent inhibitors for wild-type and mutant FGFR4
1个月前
已完结
Design, synthesis, and biological evaluation of selective covalent inhibitors of FGFR4
1个月前
已完结
Structural insights into rapamycin‐induced oligomerization of a FRB – FKBP fusion protein
1个月前
已完结
Design, synthesis, and biological evaluation of selective covalent inhibitors of FGFR4
1个月前
已完结
Optimization of Aminoindazole derivatives as highly selective covalent inhibitors for wild-type and mutant FGFR4
1个月前
已完结
Design and Synthesis of Functionally Active 5-Amino-6-Aryl Pyrrolopyrimidine Inhibitors of Hematopoietic Progenitor Kinase 1
3个月前
已完结
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