Lv11
80 积分 2021-11-11 加入
Novel dual-targeting PROTAC degraders of GSK-3β and CDK5: A promising approach for pancreatic cancer treatment
2小时前
已完结
Discovery of 5-(Pyrimidin-2-ylamino)-1H-indole-2-carboxamide Derivatives as Nur77 Modulators with Selective and Potent Activity Against Triple-Negative Breast Cancer
1个月前
已完结
Discovery of BWA-522, a First-in-Class and Orally Bioavailable PROTAC Degrader of the Androgen Receptor Targeting N-Terminal Domain for the Treatment of Prostate Cancer
5个月前
已完结
Discovery of a Series of Orally Bioavailable Androgen Receptor Degraders for the Treatment of Prostate Cancer
5个月前
已完结
Discovery of PT-65 as a highly potent and selective Proteolysis-targeting chimera degrader of GSK3 for treating Alzheimer's disease
5个月前
已完结
Discovery of Effective Dual PROTAC Degraders for Neurodegenerative Disease-Associated Aggregates
5个月前
已完结
A bibliometric analysis of PROTAC from 2001 to 2021
5个月前
已完结
Stereospecific Acylative Suzuki–Miyaura Cross-Coupling: General Access to Optically Active α-Aryl Carbonyl Compounds
6个月前
已完结
Stereoselective synthesis of all-cis boryl tetrahydroquinolines via copper-catalyzed regioselective addition/cyclization of o-aldiminyl cinnamate with B2Pin2
6个月前
已关闭
Recent Advances and Future Directions on Small Molecule VEGFR Inhibitors in Oncological Conditions
7个月前
已完结
皖公网安备34019202002308
