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108 积分 2026-08-12 加入
Discovery of CBPD-268 as an Exceptionally Potent and Orally Efficacious CBP/p300 PROTAC Degrader Capable of Achieving Tumor Regression
22天前
已完结
GNE-781, A Highly Advanced Potent and Selective Bromodomain Inhibitor of Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP)
22天前
已完结
SMARCA2 protein: Structure, function and perspectives of drug design
23天前
已完结
GNE-064: A Potent, Selective, and Orally Bioavailable Chemical Probe for the Bromodomains of SMARCA2 and SMARCA4 and the Fifth Bromodomain of PBRM1
23天前
已完结
Discovery of SMD-3040 as a Potent and Selective SMARCA2 PROTAC Degrader with Strong in vivo Antitumor Activity
28天前
已完结
Short and Scalable Synthesis of Enantiopure N‑Boc-trans-4-methyl‑L‑prolinol
1个月前
已完结
Inhibition of osimertinib-resistant epidermal growth factor receptor EGFR-T790M/C797S
1个月前
已完结
Structural Analysis of the Macrocyclic Inhibitor BI-4020 Binding to EGFR Kinase
1个月前
已完结
A Catalytic, Enantioselective Sulfamate Tethered Aza-Michael Cyclization
1个月前
已完结
Efficient Synthesis of Cyclopropane-Fused Heterocycles with Bromoethylsulfonium Salt
1个月前
已关闭
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