3R1I
| |
3P2Y
| |
3R9R
| |
3R7K
| |
3R20
| |
3R1J
| |
3RIH
| |
3RRP
| |
3R6F
| |
3R8C
| |
3FI2
| Crystal structure of JNK3 with amino-pyrazole inhibitor, SR-3451 | 分子名称: | 1,2-ETHANEDIOL, 3-{4-[(phenylcarbamoyl)amino]-1H-pyrazol-1-yl}-N-(3,4,5-trimethoxyphenyl)benzamide, Mitogen-activated protein kinase 10 | 著者 | Habel, J.E. | 登録日 | 2008-12-10 | 公開日 | 2009-03-03 | 最終更新日 | 2023-09-06 | 実験手法 | X-RAY DIFFRACTION (2.28 Å) | 主引用文献 | Structure-activity relationships and X-ray structures describing the selectivity of aminopyrazole inhibitors for c-Jun N-terminal kinase 3 (JNK3) over p38. J.Biol.Chem., 284, 2009
|
|
6WCT
| |
4IZ9
| |
6WSA
| |
3O0M
| |
6WSB
| |
3OME
| |
3OKS
| |
6XDH
| |
6XRS
| |
4KAM
| |
3FV8
| JNK3 bound to piperazine amide inhibitor, SR2774. | 分子名称: | 1,2-ETHANEDIOL, 5-bromo-N-(3-chloro-2-(4-(prop-2-ynyl)piperazin-1-yl)phenyl)furan-2-carboxamide, Mitogen-activated protein kinase 10 | 著者 | Habel, J.E. | 登録日 | 2009-01-15 | 公開日 | 2009-04-07 | 最終更新日 | 2023-09-06 | 実験手法 | X-RAY DIFFRACTION (2.28 Å) | 主引用文献 | Synthesis and SAR of piperazine amides as novel c-jun N-terminal kinase (JNK) inhibitors. Bioorg.Med.Chem.Lett., 19, 2009
|
|
3NDO
| |
3NG3
| |
3P85
| |