タイトル | The Discovery of Pamapimod, R1503 and R1487 as Orally Bioavailable and Highly Selective Inhibitors of p38 Map Kinase |
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ジャーナル・号・ページ | To be Published |
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掲載日 | 2008年12月19日 (構造データの登録日) |
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著者 | Soth, M. / Kuglstatter, A. / Goldstein, D. |
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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 | 1.8 - 2.3 Å |
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構造データ | PDB-3fln: P38 kinase crystal structure in complex with R1487 手法: X-RAY DIFFRACTION / 解像度: 1.9 Å PDB-3flq: P38 kinase crystal structure in complex with 6-(2,4-difluoro-phenoxy)-2-((s)-2-methanesulfonyl-1-methyl-ethylamino)-8-methyl-8h-pyrido[2,3-d]pyrimidin 手法: X-RAY DIFFRACTION / 解像度: 1.9 Å PDB-3fls: P38 kinase crystal structure in complex with 6-(2,4-Difluoro-phenoxy)-2-((R)-2-methanesulfonyl-1-methyl-ethylamino)-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one 手法: X-RAY DIFFRACTION / 解像度: 2.3 Å PDB-3flw: P38 kinase crystal structure in complex with pamapimod 手法: X-RAY DIFFRACTION / 解像度: 2.1 Å PDB-3fly: P38 kinase crystal structure in complex with 6-(2,4-difluoro-phenoxy)-2-isopropylamino-8-methyl-8h-pyrido[2,3-d]pyrimidin-7-one 手法: X-RAY DIFFRACTION / 解像度: 1.8 Å |
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化合物 | ChemComp-3FN: 6-(2,4-difluorophenoxy)-8-methyl-2-(tetrahydro-2H-pyran-4-ylamino)pyrido[2,3-d]pyrimidin-7(8H)-one
ChemComp-891: 6-(2,4-difluorophenoxy)-8-methyl-2-{[(1S)-1-methyl-2-(methylsulfonyl)ethyl]amino}pyrido[2,3-d]pyrimidin-7(8H)-one
ChemComp-FLS: 6-(2,4-difluorophenoxy)-8-methyl-2-{[(1R)-1-methyl-2-(methylsulfonyl)ethyl]amino}pyrido[2,3-d]pyrimidin-7(8H)-one
ChemComp-FLW: 6-(2,4-difluorophenoxy)-2-{[3-hydroxy-1-(2-hydroxyethyl)propyl]amino}-8-methylpyrido[2,3-d]pyrimidin-7(8H)-one
ChemComp-FLY: 6-(2,4-difluorophenoxy)-8-methyl-2-[(1-methylethyl)amino]pyrido[2,3-d]pyrimidin-7(8H)-one
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由来 | - homo sapiens (ヒト)
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キーワード | SIGNALING PROTEIN / TRANSFERASE / P38; MAP KINASE; SERINE/THREONINE KINASE / Alternative splicing / ATP-binding / Cytoplasm / Kinase / Nucleotide-binding / Nucleus / Phosphoprotein / Polymorphism / Serine/threonine-protein kinase |
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