Fragment-based Lead Discovery of Indazole-based Compounds as AXL Kinase Inhibitors
收藏Protein Data Bank Japan2023-11-29 更新2026-03-21 收录
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Fragment-based Lead Discovery of Indazole-based Compounds as AXL Kinase Inhibitors Descriptor: 3-[4-[6-chloranyl-5-[[(3R)-pyrrolidin-3-yl]amino]-1H-indazol-3-yl]pyrazol-1-yl]benzenecarbonitrile, Tyrosine-protein kinase Mer Authors: Anantharajan, J, Baburajendran, N. Deposit date: 2021-01-19 Release date: 2021-10-13 Last modified: 2023-11-29 Method: X-RAY DIFFRACTION (3.146 Å) Cite: Fragment-based lead discovery of indazole-based compounds as AXL kinase inhibitors. Bioorg.Med.Chem., 49, 2021
基于片段的吲唑类化合物作为AXL激酶抑制剂的先导发现研究
描述物：3-[4-[6-氯-5-[[(3R)-吡咯烷-3-基]氨基]-1H-吲唑-3-基]吡唑-1-基]苯甲腈、酪氨酸蛋白激酶Mer
作者：Anantharajan J、Baburajendran N
提交日期：2021-01-19
发布日期：2021-10-13
最后修改日期：2023-11-29
实验方法：X射线衍射（3.146 Å）
引用文献：Fragment-based lead discovery of indazole-based compounds as AXL kinase inhibitors. Bioorg.Med.Chem., 49, 2021
创建时间：
2021-01-19
