Lv21
132 积分 2025-05-19 加入
A unique inhibitor binding site in ERK1/2 is associated with slow binding kinetics
9小时前
已完结
E7766, a Macrocycle-Bridged Stimulator of Interferon Genes (STING) Agonist with Potent Pan-Genotypic Activity
3天前
已完结
Rat somatic genome editing enables ER+ breast cancer modeling
24天前
已完结
Design, Synthesis, and Pharmacological Evaluation of cGAS/HDAC Dual Inhibitors for Treatment of Autoimmune Diseases
1个月前
已完结
Photosensitizer proximity labeling captures the lipid and protein interactomes
2个月前
已完结
Design, Synthesis and Biological Evaluation of 7-(1-Methyl-1H-indole-3-yl)-5H-pyrrolo[2,3-b]pyrazine Derivatives as Novel Covalent pan-FGFR Inhibitors to Overcome Clinical Resistance
3个月前
已完结
Structure-Based Design of 4-(1-Methyl-1 H -indol-3-yl)pyrimidin-2-amine Derivatives as the First Covalent FGFR3 Selective Inhibitors
3个月前
已完结
Development of UM-200: A Novel Alkyne Amide-Based Inhibitor of the cGAS-STING Pathway
3个月前
已完结
Development of Dihydroquinoxalinone-Based Dual CDK6/BET Inhibitors for Triple-Negative Breast Cancer Therapy
4个月前
已完结
Structure-Based Design of 4-(1-Methyl-1 H -indol-3-yl)pyrimidin-2-amine Derivatives as the First Covalent FGFR3 Selective Inhibitors
5个月前
已完结
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