タイトル | From Mm Fragments to Nm Compounds Using Iloe-NMR to Guide Linking of Compounds in Fragment Based Drug Discovery (Fbdd). |
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ジャーナル・号・ページ | To be Published |
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掲載日 | 2014年11月20日 (構造データの登録日) |
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著者 | Jacso, T. / Ullah, V. / Sandmark, J. / Oster, L. / Redzick, A. / Borjesson, U. / Olsson, T. / Akerud, T. |
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リンク | PubMedで検索 |
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手法 | X線回折 |
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解像度 | 1.62 - 2.33 Å |
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構造データ | PDB-4d76: Human FXIa in complex with small molecule inhibitors. 手法: X-RAY DIFFRACTION / 解像度: 1.77 Å PDB-4d7f: Human FXIa in complex with small molecule inhibitors. 手法: X-RAY DIFFRACTION / 解像度: 1.62 Å PDB-4d7g: Human FXIa in complex with small molecule inhibitors. 手法: X-RAY DIFFRACTION / 解像度: 2.33 Å |
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化合物 | ChemComp-J1J: N-[(2S)-1-({5-[(diaminomethylidene)amino]pentyl}amino)-1-oxo-3-phenylpropan-2-yl]-4-hydroxy-2-oxo-1,2-dihydroquinoline-6-carboxamide
ChemComp-IXA: N-[(2S)-1-({4-[(diaminomethylidene)amino]butyl}amino)-1-oxo-3-phenylpropan-2-yl]-4-hydroxy-2-oxo-1,2-dihydroquinoline-6-carboxamide
ChemComp-E6U: N-[(1S)-1-benzyl-2-(3-guanidinopropylamino)-2-oxo-ethyl]-4-hydroxy-2-oxo-1H-quinoline-6-carboxamide
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由来 | homo sapiens (ヒト)
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キーワード | HYDROLASE / SERINE PROTEASE |
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