Lv4
446 积分 2024-08-26 加入
Engineering ERα degraders with pleiotropic ubiquitin ligase ligands maximizes therapeutic efficacy by co-opting distinct effector ligases
2个月前
已完结
Study on the structure-activity relationship of dihydroartemisinin derivatives: Discovery, synthesis, and biological evaluation of dihydroartemisinin-bile acid conjugates as potential anticancer agents
2个月前
已完结
The landscape of small-molecule prodrugs
4个月前
已完结
Design, Optimization, and Biological Evaluation of First-in-Class Triple Inhibitors of SGLT1, SGLT2, and DPP4 for Type 2 Diabetes Mellitus
5个月前
已完结
Elucidating Binding Selectivity in Cyclin-Dependent Kinases (CDKs) 4, 6, and 9: Development of Highly Potent and Selective CDK4/9 Inhibitors
5个月前
已完结
Small Molecule–Drug Conjugates Emerge as a New Promising Approach for Cancer Treatment
7个月前
已完结
Recent Advances in Peptide Linkers of Antibody–Drug Conjugates
7个月前
已完结
New, General, and Practical Enamine Cyclopropanation Using Dichloromethane
8个月前
已完结
Synthesis of 1- and 1,2-Substituted Cyclopropylamines from Ketone Homoenolates
8个月前
已完结
Discovery of (4-Pyrazolyl)-2-aminopyrimidines as Potent and Selective Inhibitors of Cyclin-Dependent Kinase 2
8个月前
已完结
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