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6UCS

Discovery and Structure-Based optimization of potent and selective WDR5 inhibitors containing a dihydroisoquinolinone bicyclic core

6UCS の概要
エントリーDOI10.2210/pdb6ucs/pdb
分子名称WD repeat-containing protein 5, 2-amino-3-{[(5P)-2-[(3,5-dimethoxyphenyl)methyl]-5-(4-fluoro-2-methylphenyl)-1-oxo-1,2,3,4-tetrahydroisoquinolin-7-yl]methyl}-1-methyl-1H-imidazol-3-ium (3 entities in total)
機能のキーワードwdr5, structure-based design, mixed-lineage leukemia, transcription
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数2
化学式量合計69813.18
構造登録者
Zhao, B. (登録日: 2019-09-17, 公開日: 2020-01-01, 最終更新日: 2024-05-15)
主引用文献Tian, J.,Teuscher, K.B.,Aho, E.R.,Alvarado, J.R.,Mills, J.J.,Meyers, K.M.,Gogliotti, R.D.,Han, C.,Macdonald, J.D.,Sai, J.,Shaw, J.G.,Sensintaffar, J.L.,Zhao, B.,Rietz, T.A.,Thomas, L.R.,Payne, W.G.,Moore, W.J.,Stott, G.M.,Kondo, J.,Inoue, M.,Coffey, R.J.,Tansey, W.P.,Stauffer, S.R.,Lee, T.,Fesik, S.W.
Discovery and Structure-Based Optimization of Potent and Selective WD Repeat Domain 5 (WDR5) Inhibitors Containing a Dihydroisoquinolinone Bicyclic Core.
J.Med.Chem., 63:656-675, 2020
Cited by
PubMed: 31858797
DOI: 10.1021/acs.jmedchem.9b01608
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.85 Å)
構造検証レポート
Validation report summary of 6ucs
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-08-21に公開中

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