Lv1
98 积分 2025-05-08 加入
An open-source drug discovery platform enables ultra-large virtual screens
1个月前
已完结
Combining IC50 or Ki Values From Different Sources is a Source of Significant Noise
1个月前
已完结
Deep contrastive learning enables genome-wide virtual screening
2个月前
已完结
Targeting the Spliceosomal Protein USP39 Through Allosteric Ligands and PROTAC‐Induced Degradation
4个月前
已完结
Development of selective FGFR1 degraders using a Rapid synthesis of proteolysis targeting Chimera (Rapid-TAC) platform
5个月前
已完结
Cancer Selective Target Degradation by Folate-Caged PROTACs
5个月前
已完结
Discovery of novel potent covalent inhibitor-based EGFR degrader with excellent in vivo efficacy
5个月前
已完结
Targeted Protein Degradation Induced by HEMTACs Based on HSP90
7个月前
已完结
Extracellular HSP90 Machineries Build Tumor Microenvironment and Boost Cancer Progression
7个月前
已完结
Pan- and isoform-specific inhibition of Hsp90: Design strategy and recent advances
7个月前
已完结
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