Lv61
1700 积分 2024-12-11 加入
Design and Synthesis of Pyrrolo[2,3-d]pyrimidine-Derived Leucine-Rich Repeat Kinase 2 (LRRK2) Inhibitors Using a Checkpoint Kinase 1 (CHK1)-Derived Crystallographic Surrogate
19天前
已完结
Synthetic Approaches to the New Drugs Approved During 2020
19天前
已完结
Antibacterial oxazolidinone analogues having a N-hydroxyacetyl-substituted seven-membered [1,2,5]triazepane or [1,2,5]oxadiazepane C-ring unit
2个月前
已完结
Structure-based design and optimization lead to the identification of novel potent sEH inhibitor with PPARγ partial agonist activity against inflammatory and metabolic-related diseases
4个月前
已完结
The past, present, and future of antibiotics
5个月前
已完结
Structural basis for context-specific inhibition of translation by oxazolidinone antibiotics
7个月前
已完结
Structural basis for context-specific inhibition of translation by oxazolidinone antibiotics
7个月前
已完结
Investigation of the Mechanism of Action of Oxazolidinones
7个月前
已关闭
Oxazolidinones: mechanisms of resistance and mobile genetic elements involved
7个月前
已完结
Dose optimization of TBI-223 for enhanced therapeutic benefit compared to linezolid in antituberculosis regimen
7个月前
已完结
The entanglement of a two two-level atoms interacting with a cavity field in the presence of intensity-dependent coupling regime, atom–atom, dipole–dipole interactions and Kerr-like medium
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