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8BR7

Discovery of IRAK4 Inhibitors BAY1834845 and BAY1830839

これはPDB形式変換不可エントリーです。
8BR7 の概要
エントリーDOI10.2210/pdb8br7/pdb
分子名称Interleukin-1 receptor-associated kinase 4, N-{2-[2-(4-benzoylpiperazin-1-yl)-2-oxoethyl]-2H-indazol-5-yl}-3-nitrobenzamide (3 entities in total)
機能のキーワードirak4, kinase, transferase
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67598.20
構造登録者
主引用文献Bothe, U.,Gunther, J.,Nubbemeyer, R.,Siebeneicher, H.,Ring, S.,Bomer, U.,Peters, M.,Rausch, A.,Denner, K.,Himmel, H.,Sutter, A.,Terebesi, I.,Lange, M.,Wengner, A.M.,Guimond, N.,Thaler, T.,Platzek, J.,Eberspacher, U.,Schafer, M.,Steuber, H.,Zollner, T.M.,Steinmeyer, A.,Schmidt, N.
Discovery of IRAK4 Inhibitors BAY1834845 (Zabedosertib) and BAY1830839 .
J.Med.Chem., 67:1225-1242, 2024
Cited by
PubMed Abstract: Interleukin-1 receptor-associated kinase 4 (IRAK4) plays a critical role in innate inflammatory processes. Here, we describe the discovery of two clinical candidate IRAK4 inhibitors, (zabedosertib) and , starting from a high-throughput screening hit derived from Bayer's compound library. By exploiting binding site features distinct to IRAK4 using an in-house docking model, liabilities of the original hit could surprisingly be overcome to confer both candidates with a unique combination of good potency and selectivity. Favorable DMPK profiles and activity in animal inflammation models led to the selection of these two compounds for clinical development in patients.
PubMed: 38228402
DOI: 10.1021/acs.jmedchem.3c01714
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.119 Å)
構造検証レポート
Validation report summary of 8br7
検証レポート(詳細版)ダウンロードをダウンロード

252091

件を2026-04-15に公開中

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