1KSE
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![BU of 1kse by Molmil](/molmil-images/mine/1kse) | Solution Structure of a quinolone-capped DNA duplex | 分子名称: | 5'-D(*(5AT)P*GP*CP*GP*CP*A)-3', OXOLINIC ACID | 著者 | Tuma, J, Connors, W.H, Stitelman, D.H, Richert, C. | 登録日 | 2002-01-12 | 公開日 | 2002-05-08 | 最終更新日 | 2024-05-22 | 実験手法 | SOLUTION NMR | 主引用文献 | On the effect of covalently appended quinolones on termini of DNA duplexes. J.Am.Chem.Soc., 124, 2002
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4WVT
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![BU of 4wvt by Molmil](/molmil-images/mine/4wvt) | Crystal structure of XIAP-BIR2 domain complexed with ligand bound | 分子名称: | 3,11-DIFLUORO-6,8,13-TRIMETHYL-8H-QUINO[4,3,2-KL]ACRIDIN-13-IUM, E3 ubiquitin-protein ligase XIAP, ZINC ION | 著者 | Pokross, M.E. | 登録日 | 2014-11-07 | 公開日 | 2015-03-04 | 最終更新日 | 2015-04-08 | 実験手法 | X-RAY DIFFRACTION (1.96 Å) | 主引用文献 | The Discovery of Macrocyclic XIAP Antagonists from a DNA-Programmed Chemistry Library, and Their Optimization To Give Lead Compounds with in Vivo Antitumor Activity. J.Med.Chem., 58, 2015
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4WVU
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![BU of 4wvu by Molmil](/molmil-images/mine/4wvu) | CRYSTAL STRUCTURE OF XIAP-BIR2 DOMAIN COMPLEXED WITH LIGAND BOUND | 分子名称: | 3,11-DIFLUORO-6,8,13-TRIMETHYL-8H-QUINO[4,3,2-KL]ACRIDIN-13-IUM, E3 ubiquitin-protein ligase XIAP, GLYCEROL, ... | 著者 | Pokross, M.E. | 登録日 | 2014-11-07 | 公開日 | 2015-03-04 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.02 Å) | 主引用文献 | The Discovery of Macrocyclic XIAP Antagonists from a DNA-Programmed Chemistry Library, and Their Optimization To Give Lead Compounds with in Vivo Antitumor Activity. J.Med.Chem., 58, 2015
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4WVS
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![BU of 4wvs by Molmil](/molmil-images/mine/4wvs) | Crystal structure of XIAP-BIR2 domain complexed with (S)-3-(4-methoxyphenyl)-2-((S)-2-((S)-1-((S)-2-((S)-2-(methylamino)propanamido)pent-4-ynoyl)pyrrolidine-2-carboxamido)-3-phenylpropanamido)propanoic acid | 分子名称: | 3,11-DIFLUORO-6,8,13-TRIMETHYL-8H-QUINO[4,3,2-KL]ACRIDIN-13-IUM, E3 ubiquitin-protein ligase XIAP, GLYCEROL, ... | 著者 | Pokross, M.E. | 登録日 | 2014-11-07 | 公開日 | 2015-05-06 | 最終更新日 | 2023-11-15 | 実験手法 | X-RAY DIFFRACTION (2.09 Å) | 主引用文献 | The Discovery of Macrocyclic XIAP Antagonists from a DNA-Programmed Chemistry Library, and Their Optimization To Give Lead Compounds with in Vivo Antitumor Activity. J.Med.Chem., 58, 2015
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