タイトル | Structure-Based Drug Design of RN486, a Potent and Selective Bruton's Tyrosine Kinase (BTK) Inhibitor, for the Treatment of Rheumatoid Arthritis. |
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ジャーナル・号・ページ | J. Med. Chem., Vol. 58, Page 512-516, Year 2015 |
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掲載日 | 2014年2月13日 (構造データの登録日) |
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著者 | Lou, Y. / Han, X. / Kuglstatter, A. / Kondru, R.K. / Sweeney, Z.K. / Soth, M. / McIntosh, J. / Litman, R. / Suh, J. / Kocer, B. ...Lou, Y. / Han, X. / Kuglstatter, A. / Kondru, R.K. / Sweeney, Z.K. / Soth, M. / McIntosh, J. / Litman, R. / Suh, J. / Kocer, B. / Davis, D. / Park, J. / Frauchiger, S. / Dewdney, N. / Zecic, H. / Taygerly, J.P. / Sarma, K. / Hong, J. / Hill, R.J. / Gabriel, T. / Goldstein, D.M. / Owens, T.D. |
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リンク | J. Med. Chem. / PubMed:24712864 |
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手法 | X線回折 |
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解像度 | 1.55 - 2.05 Å |
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構造データ | PDB-4ot5: Crystal structure of BTK kinase domain complexed with 4-tert-Butyl-N-(3-{8-[4-(4-methyl-piperazine-1-carbonyl)-phenylamino]-imidazo[1,2-a]pyrazin-6-yl}-phenyl)-benzamide 手法: X-RAY DIFFRACTION / 解像度: 1.55 Å PDB-4ot6: Crystal structure of BTK kinase domain complexed with 4-Methanesulfonyl-N-(3-{8-[4-(morpholine-4-carbonyl)-phenylamino]-imidazo[1,2-a]pyrazin-6-yl}-phenyl)-benzamide 手法: X-RAY DIFFRACTION / 解像度: 2.05 Å PDB-4otq: Crystal structure of BTK kinase domain complexed with 1-[5-[3-(7-tert-butyl-4-oxo-quinazolin-3-yl)-2-methyl-phenyl]-1-methyl-2-oxo-3-pyridyl]-3-methyl-urea 手法: X-RAY DIFFRACTION / 解像度: 1.55 Å PDB-4otr: Crystal structure of BTK kinase domain complexed with 6-cyclopropyl-2-[3-[5-[[5-(4-ethylpiperazin-1-yl)-2-pyridyl]amino]-1-methyl-6-oxo-3-pyridyl]-2-(hydroxymethyl)phenyl]-8-fluoro-isoquinolin-1-one 手法: X-RAY DIFFRACTION / 解像度: 1.95 Å |
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化合物 | ChemComp-481: 4-tert-butyl-N-{3-[8-({4-[(4-methylpiperazin-1-yl)carbonyl]phenyl}amino)imidazo[1,2-a]pyrazin-6-yl]phenyl}benzamide
ChemComp-2V1: 4-(methylsulfonyl)-N-[3-(8-{[4-(morpholin-4-ylcarbonyl)phenyl]amino}imidazo[1,2-a]pyrazin-6-yl)phenyl]benzamide
ChemComp-2V2: 1-{5-[3-(7-tert-butyl-4-oxoquinazolin-3(4H)-yl)-2-methylphenyl]-1-methyl-2-oxo-1,2-dihydropyridin-3-yl}-3-methylurea
ChemComp-2V3: 6-cyclopropyl-2-[3-(5-{[5-(4-ethylpiperazin-1-yl)pyridin-2-yl]amino}-1-methyl-6-oxo-1,6-dihydropyridin-3-yl)-2-(hydroxymethyl)phenyl]-8-fluoroisoquinolin-1(2H)-one
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由来 | - homo sapiens (ヒト)
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キーワード | TRANSFERASE/TRANSFERASE INHIBITOR / TRANSFERASE-TRANSFERASE INHIBITOR complex |
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