Co-structure of BTK kinase domain with L-005298385 inhibitor
收藏Protein Data Bank Japan2024-03-06 更新2026-03-21 收录
下载链接：
https://pdbj.org/mine/summary/6x3p
下载链接
链接失效反馈官方服务：
资源简介：
Co-structure of BTK kinase domain with L-005298385 inhibitor Descriptor: 1,2-ETHANEDIOL, 2-[BIS-(2-HYDROXY-ETHYL)-AMINO]-2-HYDROXYMETHYL-PROPANE-1,3-DIOL, 4-{8-amino-3-[(6R,8aS)-3-oxooctahydroindolizin-6-yl]imidazo[1,5-a]pyrazin-1-yl}-3-(cyclopropyloxy)-N-[4-(trifluoromethyl)pyridin-2-yl]benzamide, ... Authors: Fischmann, T.O. Deposit date: 2020-05-21 Release date: 2020-07-22 Last modified: 2024-03-06 Method: X-RAY DIFFRACTION (1.34 Å) Cite: Potent, non-covalent reversible BTK inhibitors with 8-amino-imidazo[1,5-a]pyrazine core featuring 3-position bicyclic ring substitutes. Bioorg.Med.Chem.Lett., 30, 2020
创建时间：
2020-05-21
