首页> 美国卫生研究院文献>Acta Crystallographica Section C: Crystal Structure Communications >N-{N-2-(35-Difluoro­phenyl)acetyl-(S)-alanyl}-(S)-phenyl­glycine tert-butyl ester (DAPT): an inhibitor of γ-secretase revealing fine electronic and hydrogen-bonding features
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N-{N-2-(35-Difluoro­phenyl)acetyl-(S)-alanyl}-(S)-phenyl­glycine tert-butyl ester (DAPT): an inhibitor of γ-secretase revealing fine electronic and hydrogen-bonding features

机译:N- {N- 2-(35-二氟苯基)乙酰基-(S)-丙氨酰}-(S)-苯基甘氨酸叔丁酯(DAPT):γ-分泌酶的抑制剂显示出良好的电子和氢粘合功能

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摘要

The title compound, C23H26F2N2O4, is a dipeptidic inhibitor of γ-secretase, one of the enzymes involved in Alzheimer’s dis­ease. The mol­ecule adopts a compact conformation, without intra­molecular hydrogen bonds. In the crystal structure, one of the amide N atoms forms the only inter­molecular N—H⋯O hydrogen bond; the second amide N atom does not form hydrogen bonds. High-resolution synchrotron diffraction data permitted the unequivocal location and refinement without restraints of all H atoms, and the identification of the characteristic shift of the amide H atom engaged in the hydrogen bond from its ideal position, resulting in a more linear hydrogen bond. Significant residual densities for bonding electrons were revealed after the usual SHELXL refinement, and modeling of these features as additional inter­atomic scatterers (IAS) using the program PHENIX led to a significant decrease in the R factor from 0.0411 to 0.0325 and diminished the r.m.s. deviation level of noise in the final difference Fourier map from 0.063 to 0.037 e Å−3.
机译:标题化合物C23H26F2N2O4是γ-分泌酶的二肽抑制剂,γ-分泌酶是与阿尔茨海默病相关的酶之一。分子具有紧密的构象,没有分子内的氢键。在晶体结构中,一个酰胺N原子形成唯一的分子间N-H = O氢键;第二个酰胺N原子不形成氢键。高分辨率同步加速器衍射数据允许毫无疑问地进行定位和精制,而没有所有H原子的约束,并且可以确定参与氢键的酰胺H原子从其理想位置发生的特征位移,从而获得更线性的氢键。在常规的SHELXL改进后,揭示了键合电子的显着残留密度,并且使用程序PHENIX将这些特征建模为附加的原子间散射体(IAS),导致R因子从0.0411显着降低至0.0325,并降低了r.m.s.最终差傅立叶图中噪声的偏差水平从0.063到0.037 eÅ -3

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