Lv1
30 积分 2024-02-28 加入
DUBA sustains the stability of NOD2 and RIPK2 to enhance innate immune responses
2天前
已完结
Discovery of imidazopyridines containing isoindoline-1,3-dione framework as a new class of BACE1 inhibitors: Design, synthesis and SAR analysis
6个月前
已完结
Design, synthesis, and biological evaluation of selective covalent inhibitors of FGFR4
6个月前
已完结
Curcumin Analog L48H37 Prevents Lipopolysaccharide-Induced TLR4 Signaling Pathway Activation and Sepsis via Targeting MD2
9个月前
已完结
Novel sulfanylphthalimide analogues as highly potent inhibitors of monoamine oxidase B
10个月前
已完结
A selective Fibroblast Growth Factor Receptor 1/2 PROTAC degrader with antitumor activity
1年前
已完结
Discovery and characterization of highly potent and selective allosteric USP7 inhibitors
1年前
已完结
Structure–activity relationship, kinetic mechanism, and selectivity for a new class of ubiquitin C-terminal hydrolase-L1 (UCH-L1) inhibitors
1年前
已完结
Discovery of a Potent and Selective Degrader for USP7
1年前
已完结
Structure–activity relationship, kinetic mechanism, and selectivity for a new class of ubiquitin C-terminal hydrolase-L1 (UCH-L1) inhibitors
1年前
已完结
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