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Crystal Structure of a Noncovalently Bound alpha-Ketoheterocycle Inhibitor (Phenhexyl/Oxadiazole/Pyridine) to a Humanized Variant of Fatty Acid Amide Hydrolase

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Protein Data Bank Japan2023-09-06 更新2026-03-21 收录
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Crystal Structure of a Noncovalently Bound alpha-Ketoheterocycle Inhibitor (Phenhexyl/Oxadiazole/Pyridine) to a Humanized Variant of Fatty Acid Amide Hydrolase Descriptor: 1-DODECANOL, 7-phenyl-1-[5-(pyridin-2-yl)-1,3,4-oxadiazol-2-yl]heptan-1-one, CHLORIDE ION, ... Authors: Mileni, M, Han, G.W, Boger, D.L, Stevens, R.C. Deposit date: 2010-11-24 Release date: 2011-11-09 Last modified: 2023-09-06 Method: X-RAY DIFFRACTION (1.78 Å) Cite: Fluoride-mediated capture of a noncovalent bound state of a reversible covalent enzyme inhibitor: X-ray crystallographic analysis of an exceptionally potent alpha-ketoheterocycle inhibitor of fatty acid amide hydrolase. J.Am.Chem.Soc., 133, 2011

人源化脂肪酸酰胺水解酶(Fatty Acid Amide Hydrolase)变体与非共价结合的α-酮杂环抑制剂(苯己基/恶二唑/吡啶类)的晶体结构 描述符:1-十二烷醇、7-苯基-1-[5-(吡啶-2-基)-1,3,4-恶二唑-2-基]庚烷-1-酮、氯离子…… 作者:Mileni, M、Han, G.W、Boger, D.L、Stevens, R.C 提交日期:2010-11-24 发布日期:2011-11-09 最后修改日期:2023-09-06 实验方法:X射线衍射(X-RAY DIFFRACTION),分辨率1.78埃(Å) 引用文献:《氟化物介导捕获可逆共价酶抑制剂的非共价结合状态:脂肪酸酰胺水解酶的超强α-酮杂环抑制剂的X射线晶体学分析》,《美国化学会志》(J. Am. Chem. Soc.),第133卷,2011年
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2010-11-24
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