Lv31
320 积分 2025-09-22 加入
Discovery of Novel ERα and Aromatase Dual-Targeting PROTAC Degraders to Overcome Endocrine-Resistant Breast Cancer
14天前
已完结
Stable expression of human aromatase complementary DNA in mammalian cells: a useful system for aromatase inhibitor screening
24天前
已关闭
Arylidene-Thiazoldione Scaffold Acts as the E3 Ligand of DCAF11 for PROTAC Design
1个月前
已完结
Selective CDK6 Degradation via the KLHDC2 E3 Ubiquitin Ligase
2个月前
已完结
Rational Design of CDK12/13 and BRD4 Molecular Glue Degraders
3个月前
已完结
Abstract LB430: QTX3544, a potent and selective G12V-preferring KRAS inhibitor, synergizes with EGFR inhibitors for enhanced anti-tumor activity
3个月前
已关闭
A Glutathione S-Transferase Pi Molecular Glue Tethers Splicing Factors and Remodels Cell Metabolism
4个月前
已完结
Structural basis for LZTR1 recognition of RAS GTPases for degradation
4个月前
已完结
Discovery of BRD9 Molecular Glue Degraders That Spare Cardiomyocytes
5个月前
已完结
Rational Design of CDK12/13 and BRD4 Molecular Glue Degraders
5个月前
已完结
皖公网安备34019202002308
