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44 积分 2025-12-03 加入
Development of PROTAC degrader probe of CDK4/6 based on DCAF16
7天前
已完结
Exploration of the Tunability of BRD4 Degradation by DCAF16 Trans-labelling Covalent Glues
9天前
已完结
Discovery of benzenesulfonamide derivatives as potent PI3K/mTOR dual inhibitors with in vivo efficacies against hepatocellular carcinoma
14天前
已完结
Omipalisib inspired macrocycles as dual PI3K/mTOR inhibitors
14天前
已完结
Transient Receptor Potential Canonical 6 (TRPC6) Channel in the Pathogenesis of Diseases: A Jack of Many Trades
22天前
已完结
TRPC6 inhibition: podocyte-targeted treatment for focal segmental glomerulosclerosis?
24天前
已完结
Transient Receptor Potential Canonical 6 (TRPC6) Channel in the Pathogenesis of Diseases: A Jack of Many Trades
24天前
已完结
TRPC6: physiological function and pathophysiological relevance
28天前
已完结
Transient Receptor Potential Canonical 6 (TRPC6) Channel in the Pathogenesis of Diseases: A Jack of Many Trades
28天前
已完结
Discovery of a Potent, Selective and In Vivo Active Aurora A PROTAC Degrader from a Promiscuous Kinase Inhibitor
1个月前
已完结
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