Design and Synthesis of Highly Potent and Isoform Selective JNK3 Inhibitors: SAR Studies on Aminopyrazole Derivatives
收藏Protein Data Bank Japan2023-12-27 更新2026-03-21 收录
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https://pdbj.org/mine/summary/4whz
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Design and Synthesis of Highly Potent and Isoform Selective JNK3 Inhibitors: SAR Studies on Aminopyrazole Derivatives Descriptor: 3-(4-{[(2-chlorophenyl)carbamoyl]amino}-1H-pyrazol-1-yl)-N-{1-[(3S)-pyrrolidin-3-yl]-1H-pyrazol-4-yl}benzamide, Mitogen-activated protein kinase 10 Authors: Park, H, LoGrasso, P. Deposit date: 2014-09-24 Release date: 2014-11-26 Last modified: 2023-12-27 Method: X-RAY DIFFRACTION (1.79 Å) Cite: Design and Synthesis of Highly Potent and Isoform Selective JNK3 Inhibitors: SAR Studies on Aminopyrazole Derivatives. J.Med.Chem., 57, 2014
创建时间：
2014-09-24
