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Novel hydroxyl tricyclics (e.g. GSK966587) as potent inhibitors of bacterial type IIA topoisomerases

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Protein Data Bank Japan2023-12-20 更新2026-03-21 收录
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Novel hydroxyl tricyclics (e.g. GSK966587) as potent inhibitors of bacterial type IIA topoisomerases Descriptor: (S)-4-((4-(((2,3-dihydro-[1,4]dioxino[2,3-c]pyridin-7-yl)methyl)amino)piperidin-1-yl)methyl)-3-fluoro-4-hydroxy-4H-pyrrolo[3,2,1-de][1,5]naphthyridin-7(5H)-one, 5'-D(*AP*GP*CP*CP*GP*TP*AP*GP*GP*TP*AP*CP*AP*CP *CP*GP*CP*AP*C)-3', 5'-D(*TP*GP*TP*GP*CP*GP*GP*TP*GP*TP*AP*CP*CP*TP *AP*CP*GP*GP*CP*T)-3', ... Authors: Miles, T.J, Hennessy, A.J, Bax, B, Brooks, G, Brown, B.S, Brown, P, Cailleau, N, Chen, D, Dabbs, S, Davies, D.T, Esken, J.M, Giordano, I, Hoover, J.L, Huang, J, Jones, G.E, Sukmar, S.K.K, Spitzfaden, C, Markwell, R.E, Minthorn, E.A, Rittenhouse, S, Gwynn, M.N, Pearson, N.D. Deposit date: 2013-06-20 Release date: 2013-08-07 Last modified: 2023-12-20 Method: X-RAY DIFFRACTION (2.6 Å) Cite: Novel Hydroxyl Tricyclics (E.G., Gsk966587) as Potent Inhibitors of Bacterial Type Iia Topoisomerases. Bioorg.Med.Chem.Lett., 23, 2013

数据集主题:新型羟基三环类化合物(如GSK966587)作为强效细菌IIA型拓扑异构酶抑制剂 描述项:(S)-4-((4-(((2,3-二氢-[1,4]二噁英[2,3-c]吡啶-7-基)甲基)氨基)哌啶-1-基)甲基)-3-氟-4-羟基-4H-吡咯并[3,2,1-de][1,5]萘啶-7(5H)-酮、5'-D(*AP*GP*CP*CP*GP*TP*AP*GP*GP*TP*AP*CP*AP*CP*CP*GP*CP*AP*C)-3'、5'-D(*TP*GP*TP*GP*CP*GP*GP*TP*GP*TP*AP*CP*CP*TP*AP*CP*GP*GP*CP*T)-3' 等 作者:Miles, T.J.、Hennessy, A.J.、Bax, B、Brooks, G、Brown, B.S、Brown, P、Cailleau, N、Chen, D、Dabbs, S、Davies, D.T、Esken, J.M、Giordano, I、Hoover, J.L、Huang, J、Jones, G.E、Sukmar, S.K.K、Spitzfaden, C、Markwell, R.E、Minthorn, E.A、Rittenhouse, S、Gwynn, M.N、Pearson, N.D. 提交日期:2013年6月20日 发布日期:2013年8月7日 最后修改日期:2023年12月20日 检测方法:X射线衍射(分辨率2.6 Å) 引用文献:《新型羟基三环类化合物(如GSK966587)作为强效细菌IIA型拓扑异构酶抑制剂》,Bioorg.Med.Chem.Lett., 23, 2013
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2013-06-20
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