タイトル | Pharmacophore Mapping of Thienopyrimidine-Based Monophosphonate (ThP-MP) Inhibitors of the Human Farnesyl Pyrophosphate Synthase. |
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ジャーナル・号・ページ | J. Med. Chem., Vol. 60, Page 2119-2134, Year 2017 |
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掲載日 | 2016年5月10日 (構造データの登録日) |
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著者 | Park, J. / Leung, C.Y. / Matralis, A.N. / Lacbay, C.M. / Tsakos, M. / Fernandez De Troconiz, G. / Berghuis, A.M. / Tsantrizos, Y.S. |
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リンク | J. Med. Chem. / PubMed:28208018 |
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手法 | X線回折 |
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解像度 | 2.3 - 2.65 Å |
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構造データ | PDB-5juz: Crystal structure of human FPPS in complex with an allosteric inhibitor CL-06-057 手法: X-RAY DIFFRACTION / 解像度: 2.4 Å PDB-5jv0: Crystal structure of human FPPS in complex with an allosteric inhibitor CL-08-038 手法: X-RAY DIFFRACTION / 解像度: 2.4 Å PDB-5jv1: Crystal structure of human FPPS in complex with an allosteric inhibitor CL-08-066 手法: X-RAY DIFFRACTION / 解像度: 2.3 Å PDB-5jv2: Crystal structure of human FPPS in complex with an allosteric inhibitor MIT-01-055 手法: X-RAY DIFFRACTION / 解像度: 2.3 Å PDB-5ksx: Crystal structure of human FPPS in complex with an allosteric inhibitor AM-02-072 手法: X-RAY DIFFRACTION / 解像度: 2.65 Å |
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化合物 | ChemComp-YL4: [(R)-(2,3-dihydro-1-benzofuran-5-yl){[6-(4-methylphenyl)thieno[2,3-d]pyrimidin-4-yl]amino}methyl]phosphonic acid
ChemComp-YL5: [(1R)-2-(3-fluorophenyl)-1-{[6-(4-methylphenyl)thieno[2,3-d]pyrimidin-4-yl]amino}ethyl]phosphonic acid
ChemComp-YL6: [(1R)-1-{[6-(3-chloro-4-methylphenyl)thieno[2,3-d]pyrimidin-4-yl]amino}-2-(3-fluorophenyl)ethyl]phosphonic acid
ChemComp-6O3: {[6-(4-methylphenyl)thieno[2,3-d]pyrimidin-5-yl]methyl}phosphonic acid
ChemComp-7AM: [[(2~{S})-2-[[6-(4-methylphenyl)thieno[2,3-d]pyrimidin-4-yl]amino]-3-phenyl-propanoyl]amino]phosphonic acid
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由来 | - homo sapiens (ヒト)
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キーワード | TRANSFERASE/TRANSFERASE INHIBITOR / Transferase / TRANSFERASE-TRANSFERASE INHIBITOR complex |
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