Lv51
1004 积分 2024-02-22 加入
Design, synthesis and biological evaluation of 3-amino-6-(2-hydroxyphenyl)pyridazin-4-aryl derivatives as SMARCA2/4 degraders
3小时前
已完结
An orally active, small-molecule TNF inhibitor that disrupts the homotrimerization interface improves inflammatory arthritis in mice
1个月前
已完结
Enhancer reprogramming underlies therapeutic utility of a SMARCA2 degrader in SMARCA4 mutant cancer
1个月前
已完结
Discovery of High-Affinity SMARCA2/4 Bromodomain Ligands and Development of Potent and Exceptionally Selective SMARCA2 PROTAC Degraders
1个月前
已完结
SMARCA2 protein: structure, function and perspectives of drug design
1个月前
已完结
Azobenzene‐Based Linker Strategy for Selective Activation of Antibody–Drug Conjugates
1个月前
已完结
Potent antitumor activity of anti-HER2 antibody-topoisomerase I inhibitor conjugate based on self-immolative dendritic dimeric-linker
1个月前
已完结
Optimization of a pendant-shaped PEGylated linker for antibody-drug conjugates
1个月前
已完结
Abstract ND08: M3554, a novel anti-GD2 antibody drug conjugate
1个月前
已关闭
Targeting cancer with small molecule pan-KRAS degraders
1个月前
已完结
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