Lv3
274 积分 2025-08-07 加入
Targeting Multiple KRAS Mutations with High-Affinity Macrocyclic Inhibitors: From Discovery to Preclinical Validation
1天前
已完结
“Keep on ROCKIn”: Repurposed ROCK inhibitors to boost corneal endothelial regeneration
3天前
已完结
Discovery of unglycosylated indolocarbazoles as ROCK2 isoform-selective inhibitors for the treatment of breast cancer metastasis
5天前
已完结
Protein-templated synthesis of dinucleotide repeat DNA by an antiphage reverse transcriptase
10天前
已完结
ROCK-2-selective targeting and its therapeutic outcomes
16天前
已完结
Target identification and assessment in the era of AI
1个月前
已完结
Characteristic roadmap of linker governs the rational design of PROTACs
1个月前
已完结
Discovery of (S)-6-methoxy-chroman-3-carboxylic acid (4-pyridin-4-yl-phenyl)-amide as potent and isoform selective ROCK2 inhibitors
1个月前
已关闭
In Situ PROTAC Synthesis Enabled by Pathologically Activated Bioorthogonal Catalysis for Precision Cancer Therapy
1个月前
已完结
Development of Prostate-Specific Lysosome-Targeting Degraders
1个月前
已完结
皖公网安备34019202002308
