タイトル A potent seven-membered cyclic BTK (Bruton's tyrosine Kinase) chiral inhibitor conceived by structure-based drug design to lock its bioactive conformation. ジャーナル・号・ページ Bioorg. Med. Chem. Lett. , Vol. 29, Page 1074-1078, Year 2019掲載日 2018年9月28日 (構造データの登録日) 著者Lopez-Tapia, F. / Lou, Y. / Brotherton-Pleiss, C. / Kuglstatter, A. / So, S.S. / Kondru, R. リンク Bioorg. Med. Chem. Lett. / PubMed:30857747手法 X線回折 解像度 1.12 - 1.36 Å 構造データ PDB-6hrp : 構造ビューア CRYSTAL STRUCTURE OF BTK KINASE DOMAIN COMPLEXED WITH 6-(dimethylamino)-2-[2-(hydroxymethyl)-3-[1-methyl-5-[[5-(morpholine-4-carbonyl)-2-pyridyl]amino]-6-oxo-3-pyridyl]phenyl]-3,4-dihydroisoquinolin-1-one 手法 : X-RAY DIFFRACTION / 解像度 : 1.12 Å
PDB-6hrt : 構造ビューア CRYSTAL STRUCTURE OF BTK KINASE DOMAIN COMPLEXED WITH 12-(6-tert-butyl-8-fluoro-1-oxo-phthalazin-2-yl)-9-hydroxy-6-methyl-4-[[5-(morpholine-4-carbonyl)-2-pyridyl]amino]-6-azatricyclo[9.4.0.02,7]pentadeca-1(15),2(7),3,11,13-pentaen-5-one 手法 : X-RAY DIFFRACTION / 解像度 : 1.36 Å
化合物 ChemComp-GMQ : 構造ビューア 6-~{tert}-butyl-8-fluoranyl-2-[2-(hydroxymethyl)-3-[1-methyl-5-[(5-morpholin-4-ylcarbonylpyridin-2-yl)amino]-6-oxidanylidene-pyridazin-3-yl]phenyl]phthalazin-1-one
ChemComp-GMW : 構造ビューア (9~{S})-12-(6-~{tert}-butyl-8-fluoranyl-1-oxidanylidene-phthalazin-2-yl)-6-methyl-4-[(5-morpholin-4-ylcarbonylpyridin-2-yl)amino]-9-oxidanyl-6-azatricyclo[9.4.0.0^{2,7}]pentadeca-1(15),2(7),3,11,13-pentaen-5-one
由来 homo sapiens (ヒト) キーワード TRANSFERASE / TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX