Lv3
342 积分 2025-03-04 加入
Synthesis and structures of homoleptic germylenes and stannylenes with sulfonimidamide ligands
8天前
已完结
A Dual-Target and Dual-Mechanism Design Strategy by Combining Inhibition and Degradation Together
17天前
已完结
Discovery and Pharmacological Evaluation of Potent and Highly Selective PARP1 Inhibitors
19天前
已完结
FimH Antagonists: Phosphate Prodrugs Improve Oral Bioavailability
1个月前
已完结
Heterosynthons, Solid Form Design and Enhanced Drug Bioavailability
1个月前
已完结
N-Substituted Prodrugs of Mebendazole Provide Improved Aqueous Solubility and Oral Bioavailability in Mice and Dogs
1个月前
已完结
Acyclic cucurbit[n]uril molecular containers enhance the solubility and bioactivity of poorly soluble pharmaceuticals
1个月前
已完结
Selective PARP1 inhibitors, PARP1-based dual-target inhibitors, PROTAC PARP1 degraders, and prodrugs of PARP1 inhibitors for cancer therapy
1个月前
已完结
Double Swords in One: Novel Selective PI3K/110β PROTAC Degraders for the Treatment of Multidrug-Resistant Cancer by Activating ERS and Inhibiting P-gp
2个月前
已完结
Novel Mitochondria-Targeted Asymmetric Heptamethine Cyanine Dye for Cancer Targeted NIR Imaging and Potent Necrosis and Senescence Induction with Prolonged Retention
3个月前
已完结
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