hALK in complex with compound 7 N-((1S)-1-(5-fluoropyridin-2-yl)ethyl)-1-(5-methyl-1H-pyrazol-3-yl)-3-(oxetan-3-ylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-6-amine
收藏Protein Data Bank Japan2024-03-13 更新2026-03-21 收录
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hALK in complex with compound 7 N-((1S)-1-(5-fluoropyridin-2-yl)ethyl)-1-(5-methyl-1H-pyrazol-3-yl)-3-(oxetan-3-ylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-6-amine Descriptor: ALK tyrosine kinase receptor, N-[(1S)-1-(5-fluoropyridin-2-yl)ethyl]-1-(5-methyl-1H-pyrazol-3-yl)-3-[(oxetan-3-yl)sulfonyl]-1H-pyrrolo[2,3-b]pyridin-6-amine Authors: Lane, W, Saikatendu, K. Deposit date: 2018-07-06 Release date: 2019-05-01 Last modified: 2024-03-13 Method: X-RAY DIFFRACTION (2.303 Å) Cite: Discovery of Potent, Selective, and Brain-Penetrant 1 H-Pyrazol-5-yl-1 H-pyrrolo[2,3- b]pyridines as Anaplastic Lymphoma Kinase (ALK) Inhibitors. J.Med.Chem., 62, 2019
与化合物7 N-[(1S)-1-(5-氟吡啶-2-基)乙基]-1-(5-甲基-1H-吡唑-3-基)-3-(氧杂环丁烷-3-基磺酰基)-1H-吡咯并[2,3-b]吡啶-6-胺结合的人源ALK(hALK)。
描述信息:ALK酪氨酸激酶受体,N-[(1S)-1-(5-氟吡啶-2-基)乙基]-1-(5-甲基-1H-吡唑-3-基)-3-[(氧杂环丁烷-3-基)磺酰基]-1H-吡咯并[2,3-b]吡啶-6-胺。
作者:Lane, W、Saikatendu, K.
提交日期:2018-07-06
发布日期:2019-05-01
最后修改日期:2024-03-13
实验方法:X射线衍射(分辨率2.303 Å)
引用文献:《强效、选择性且可穿透血脑屏障的1H-吡唑-5-基-1H-吡咯并[2,3-b]吡啶类ALK抑制剂》,《Journal of Medicinal Chemistry》,2019年,第62卷。
创建时间:
2018-07-06



