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张璋
Lv7
5
3610 积分
2022-11-24 加入
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Dual Kv7.2/3-TRPV1 modulators inhibit nociceptor hyperexcitability and alleviate pain without target-related side effects
1个月前
已完结
Species-specific differences and the role of Nav1.9 in pain pathophysiology
1个月前
已完结
Persistent (Nav1.9) sodium currents in human dorsal root ganglion neurons
1个月前
已完结
Atom swap in triple bonds via nitrogen-deletion coupling with gem-diborylalkanes
2个月前
已完结
The Medicinal Chemist's Guide to Solving ADMET Challenges
2个月前
已完结
Discovery of Novel Pyrimidine-Based Derivatives as Nav1.2 Inhibitors with Efficacy in Mouse Models of Epilepsy
3个月前
已完结
Discovery of Preclinical Candidate AD1058 as a Highly Potent, Selective, and Brain-Penetrant ATR Inhibitor for the Treatment of Advanced Malignancies
3个月前
已完结
Recent advances in small molecule Nav 1.7 inhibitors for cancer pain management
4个月前
已完结
High-Throughput SFC-MS/MS Method to Measure EPSA and Predict Human Permeability
4个月前
已完结
Practical Process Research and Development
5个月前
已完结
没有进行任何应助
时间有点久【积分已退回】
1年前
求助文献标题为:Structure Based Design of CYP51 Inhibitors,发表在2016年的Curr. Top. Med. Chem.,PMID: 27449014 DOI: 10.2174/1568026616666160719164933。但应助文献为Structure-based design of PDK1 inhibitors,发表在2011年的Bioorganic & Medicinal Chemistry Letters上。
1年前
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