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123456qi
Lv4
6
570 积分
2024-03-15 加入
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Discovery of ERD-3111 as a Potent and Orally Efficacious Estrogen Receptor PROTAC Degrader with Strong Antitumor Activity
9天前
已完结
Discovery of SD-436: A Potent, Highly Selective and Efficacious STAT3 PROTAC Degrader Capable of Achieving Complete and Long-Lasting Tumor Regression
10天前
已完结
Application and challenges of nitrogen heterocycles in PROTAC linker
11天前
已完结
Potency-Enhanced Peptidomimetic VHL Ligands with Improved Oral Bioavailability
15天前
已完结
Discovery of SK-575 as a Highly Potent and Efficacious Proteolysis-Targeting Chimera Degrader of PARP1 for Treating Cancers
15天前
已完结
Functional characterization of a PROTAC directed against BRAF mutant V600E
15天前
已完结
Potency-Enhanced Peptidomimetic VHL Ligands with Improved Oral Bioavailability
17天前
已完结
Design, Synthesis and Antitumor Activity of a Novel Class of SHP2 Allosteric Inhibitors with a Furanyl Amide-Based Scaffold
17天前
已完结
Study of critical role of c-Met and its inhibitor SU11274 in colorectal carcinoma
17天前
已完结
PROTACs in Treatment of Cancer: A Review
17天前
已完结
没有进行任何应助
不需要pre-proof版,要正式版
4个月前
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