Lv1
37 积分 2021-11-02 加入
Discovery of Novel Bifunctional Agents as Potent TRK Inhibitors and Degraders against xDFG Mutation Resistance
7小时前
已完结
Discovery of YFJ-36: Design, Synthesis, and Antibacterial Activities of Catechol-Conjugated β-Lactams against Gram-Negative Bacteria
1天前
已完结
Discovery of Potent, Selective and Efficacious Aminopyrazole Inhibitors of PLK4
4天前
已完结
Discovery of HW201877: A Highly Potent and Orally Bioavailable Inhibitor of 15-Prostaglandin Dehydrogenase to Potentiate Tissue Repair and Regeneration
4天前
已完结
Discovery of Bis-imidazolecarboxamide Derivatives as Novel, Potent, and Selective TNIK Inhibitors for the Treatment of Idiopathic Pulmonary Fibrosis
6天前
已完结
NSD2 targeting reverses plasticity and drug resistance in prostate cancer
9天前
已完结
Design, Synthesis, and Characterization of GluN2A Negative Allosteric Modulators Suitable for In Vivo Exploration
12天前
已完结
GluN2A mediates ketamine-induced rapid antidepressant-like responses
13天前
已完结
Bespoke library docking for 5-HT2A receptor agonists with antidepressant activity
13天前
已完结
Pathway-selective 5-HT1AR agonist as a rapid antidepressant strategy
14天前
已完结
皖公网安备34019202002308
