| タイトル | Discovery of novel integrase-LEDGF/p75 allosteric inhibitors based on a benzene scaffold. |
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| ジャーナル・号・ページ | Bioorg. Med. Chem., Vol. 28, Page 115643-115643, Year 2020 |
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| 掲載日 | 2019年12月25日 (構造データの登録日) |
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著者 | Sugiyama, S. / Iwaki, T. / Tamura, Y. / Tomita, K. / Matsuoka, E. / Arita, S. / Seki, T. / Yoshinaga, T. / Kawasuji, T. |
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リンク | Bioorg. Med. Chem. / PubMed:32773094 |
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| 手法 | X線回折 |
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| 解像度 | 2.1 - 2.5 Å |
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| 構造データ | PDB-6lmi: Crystal structure of HIV-1 integrase catalytic core domain in complex with 2-(tert-butoxy)-2-[3-(3,4-dihydro-2H-1-benzopyran-6-yl)-6-methanesulfonamido-2,3',4',5-tetramethyl-[1,1'-biphenyl]-4-yl]acetic acid 手法: X-RAY DIFFRACTION / 解像度: 2.5 Å PDB-6lmq: Crystal structure of HIV-1 integrase catalytic core domain in complex with 2-(tert-butoxy)-2-[3-(3,4-dihydro-2H-1,4-benzoxazin-6-yl)-6-methanesulfonamido-2,3',4',5-tetramethyl-[1,1'-biphenyl]-4-yl]acetic acid 手法: X-RAY DIFFRACTION / 解像度: 2.1 Å |
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| 化合物 | ChemComp-EJ9: (2S)-2-[2-(3,4-dihydro-2H-chromen-6-yl)-4-(3,4-dimethylphenyl)-3,6-dimethyl-5-(methylsulfonylamino)phenyl]-2-[(2-methylpropan-2-yl)oxy]ethanoic acid
ChemComp-940: (2S)-2-[2-(3,4-dihydro-2H-1,4-benzoxazin-6-yl)-4-(3,4-dimethylphenyl)-3,6-dimethyl-5-(methylsulfonylamino)phenyl]-2-[(2-methylpropan-2-yl)oxy]ethanoic acid
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| 由来 | human immunodeficiency virus type 1 group m subtype b (isolate ny5) (ヒト免疫不全ウイルス)
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キーワード | TRANSFERASE / hydrolase transferase/inhibitor |
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