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HIV-1 protease in complex with fluoro substituted diol-based C2- symmetric inhibitor

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Protein Data Bank Japan2024-05-08 更新2026-03-21 收录
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HIV-1 protease in complex with fluoro substituted diol-based C2- symmetric inhibitor Descriptor: (2R,3R,4R,5R)-2,5-BIS[(2,5-DIFLUOROBENZYL)OXY]-3,4-DIHYDROXY-N,N'-BIS[(1S,2R)-2-HYDROXY-2,3-DIHYDRO-1H-INDEN-1-YL]HEXANEDIAMIDE, POL POLYPROTEIN Authors: Lindberg, J, Pyring, D, Loewgren, S, Rosenquist, A, Zuccarello, G, Kvarnstroem, I, Zhang, H, Vrang, L, Claesson, B, Hallberg, A, Samuelsson, B, Unge, T. Deposit date: 2004-08-10 Release date: 2004-10-07 Last modified: 2024-05-08 Method: X-RAY DIFFRACTION (1.9 Å) Cite: Symmetric Fluoro-Substituted Diol-Based HIV Protease Inhibitors. Ortho-Fluorinated and Meta-Fluorinated P1/P1'-Benzyloxy Side Groups Significantly Improve the Antiviral Activity and Preserve Binding Efficacy Eur.J.Biochem., 271, 2004

与氟取代二醇类C₂对称抑制剂结合的HIV-1蛋白酶(HIV-1 protease) 描述物:(2R,3R,4R,5R)-2,5-双[(2,5-二氟苄基)氧基]-3,4-二羟基-N,N'-双[(1S,2R)-2-羟基-2,3-二氢-1H-茚-1-基]己二酰胺,POL多聚蛋白(POL polyprotein) 作者:Lindberg, J、Pyring, D、Loewgren, S、Rosenquist, A、Zuccarello, G、Kvarnstroem, I、Zhang, H、Vrang, L、Claesson, B、Hallberg, A、Samuelsson, B、Unge, T 提交日期:2004-08-10 发布日期:2004-10-07 最后修改日期:2024-05-08 实验方法:X射线衍射(X-RAY DIFFRACTION),分辨率1.9埃(Å) 引用文献:《对称氟取代二醇类HIV蛋白酶抑制剂:邻氟与间氟取代的P1/P1'-苄氧基侧链可显著提升抗病毒活性并保持结合效力》,《欧洲生物化学杂志》(Eur.J.Biochem.),第271卷,2004年
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2004-08-10
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