PKA structures of AKT, indazole-pyridine inhibitors
收藏Protein Data Bank Japan2024-05-08 更新2026-03-21 收录
下载链接：
https://pdbj.org/mine/summary/2uzt
下载链接
链接失效反馈官方服务：
资源简介：
PKA structures of AKT, indazole-pyridine inhibitors Descriptor: (2S)-1-{[5-(3-METHYL-1H-INDAZOL-5-YL)PYRIDIN-3-YL]OXY}-3-PHENYLPROPAN-2-AMINE, CAMP-DEPENDENT PROTEIN KINASE INHIBITOR ALPHA, CAMP-DEPENDENT PROTEIN KINASE, ... Authors: Zhu, G.D, Gandhi, V.B, Gong, J, Thomas, S, Woods, K.W, Song, X, Li, T, Diebold, R.B, Luo, Y, Liu, X, Guan, R, Klinghofer, V, Johnson, E.F, Bouska, J, Olson, A, Marsh, K.C, Stoll, V.S, Mamo, M, Polakowski, J, Campbell, T.J, Penning, T.D, Li, Q, Rosenberg, S.H, Giranda, V.L. Deposit date: 2007-05-01 Release date: 2007-06-05 Last modified: 2024-05-08 Method: X-RAY DIFFRACTION (2.1 Å) Cite: Syntheses of Potent, Selective, and Orally Bioavailable Indazole-Pyridine Series of Protein Kinase B/Akt Inhibitors with Reduced Hypotension. J.Med.Chem., 50, 2007
创建时间：
2007-05-01
