Lv72
3610 积分 2024-02-10 加入
Design and synthesis of Riluzole-Ciprofloxacin hybrids as selective MST3 inhibitors for cancer treatment
3天前
已完结
Structure Based Drug Design of Crizotinib (PF-02341066), a Potent and Selective Dual Inhibitor of Mesenchymal–Epithelial Transition Factor (c-MET) Kinase and Anaplastic Lymphoma Kinase (ALK)
5天前
已完结
Tea catechins as inhibitors of receptor tyrosine kinases: mechanistic insights and human relevance
6天前
已完结
Computational insights into the stereo-selectivity of catechins for the inhibition of the cancer therapeutic target EGFR kinase
6天前
已完结
Inhibition of the epidermal growth factor receptor tyrosine kinase activity by leflunomide
6天前
已完结
Fluorocyclopropyl-containing tacrine derivatives as potent and selective dual CDK2/CDK9 inhibitors for the treatment of colorectal cancer
6天前
已完结
Design, Synthesis, and SAR of Covalent KIT and PDGFRA Inhibitors─Exploring Their Potential in Targeting GIST
13天前
已完结
Repurposing food and drug administration-approved cancer therapies: Exploring endocrine and targeted pathways in low-grade serous ovarian cancer treatment
1个月前
已关闭
The future of immune checkpoint therapy
1个月前
已完结
Crystal structure of the catalytic subunit of cyclic adenosine monophosphate-dependent protein kinase
1个月前
已完结
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