タイトル | Selection of fragments for kinase inhibitor design: decoration is key. |
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ジャーナル・号・ページ | J. Med. Chem., Vol. 58, Page 457-465, Year 2015 |
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掲載日 | 2014年11月21日 (構造データの登録日) |
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著者 | Czodrowski, P. / Holzemann, G. / Barnickel, G. / Greiner, H. / Musil, D. |
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リンク | J. Med. Chem. / PubMed:25437144 |
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手法 | X線回折 |
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解像度 | 1.49 - 2.5 Å |
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構造データ | PDB-4x0m: Selection of fragments for kinase inhibitor design: decoration is key 手法: X-RAY DIFFRACTION / 解像度: 1.68 Å PDB-4x2f: Selection of fragments for kinase inhibitor design: decoration is key 手法: X-RAY DIFFRACTION / 解像度: 1.49 Å PDB-4x2g: Selection of fragments for kinase inhibitor design: decoration is key 手法: X-RAY DIFFRACTION / 解像度: 1.51 Å PDB-4x2j: Selection of fragments for kinase inhibitor design: decoration is key 手法: X-RAY DIFFRACTION / 解像度: 1.69 Å PDB-4x2k: Selection of fragments for kinase inhibitor design: decoration is key 手法: X-RAY DIFFRACTION / 解像度: 1.69 Å PDB-4x2n: Selection of fragments for kinase inhibitor design: decoration is key 手法: X-RAY DIFFRACTION / 解像度: 1.8 Å PDB-4x3j: Selection of fragments for kinase inhibitor design: decoration is key 手法: X-RAY DIFFRACTION / 解像度: 2.5 Å |
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化合物 | ChemComp-3WJ: 4-amino-8-(4-aminophenyl)pyrido[2,3-d]pyrimidin-5(8H)-one
ChemComp-3WK: 4-[(4-aminophenyl)amino]pyrido[2,3-d]pyrimidin-5(6H)-one
ChemComp-3WN: 4-[(3-aminophenyl)amino]pyrido[2,3-d]pyrimidin-5(8H)-one
ChemComp-3WO: 4-[(3-aminophenyl)amino]pyrido[2,3-d]pyrimidin-5(6H)-one
ChemComp-3WR: 1-[4-(4-amino-5-oxopyrido[2,3-d]pyrimidin-8(5H)-yl)phenyl]-3-[2-fluoro-5-(trifluoromethyl)phenyl]urea
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由来 | ![](img/tx_human.gif) homo sapiens (ヒト)
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キーワード | TRANSFERASE (転移酵素) / PROTEIN KINASE (プロテインキナーゼ) / INHIBITOR COMPLEX (酵素阻害剤) / Transferase/Transferase Inhibitor / Transferase-Transferase Inhibitor complex |
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