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7N5O

Fragment-Based Discovery of a Novel Bruton's Tyrosine Kinase Inhibitor

7N5O の概要
エントリーDOI10.2210/pdb7n5o/pdb
分子名称Tyrosine-protein kinase BTK, IMIDAZOLE, S-1,2-PROPANEDIOL, ... (6 entities in total)
機能のキーワードcytoplasmic tyrosine kinase, transcriptional regulation, nuclear factor-kappab, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数1
化学式量合計33098.94
構造登録者
Dougan, D.R.,Lawson, J.D. (登録日: 2021-06-06, 公開日: 2021-09-08, 最終更新日: 2023-10-18)
主引用文献Sabat, M.,Dougan, D.R.,Knight, B.,Lawson, J.D.,Scorah, N.,Smith, C.R.,Taylor, E.R.,Vu, P.,Wyrick, C.,Wang, H.,Balakrishna, D.,Hixon, M.,Madakamutil, L.,McConn, D.
Discovery of the Bruton's Tyrosine Kinase Inhibitor Clinical Candidate TAK-020 ( S )-5-(1-((1-Acryloylpyrrolidin-3-yl)oxy)isoquinolin-3-yl)-2,4-dihydro-3 H -1,2,4-triazol-3-one, by Fragment-Based Drug Design.
J.Med.Chem., 64:12893-12902, 2021
Cited by
PubMed: 34448571
DOI: 10.1021/acs.jmedchem.1c01026
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.25 Å)
構造検証レポート
Validation report summary of 7n5o
検証レポート(詳細版)ダウンロードをダウンロード

222415

件を2024-07-10に公開中

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