
N ‐{ N ‐[2‐(3,5‐Difluorophenyl)acetyl]‐( S )‐alanyl}‐( S )‐phenylglycine tert ‐butyl ester (DAPT): an inhibitor of γ‐secretase, revealing fine electronic and hydrogen‐bonding features
Author(s) -
Czerwinski Andrzej,
Valenzuela Francisco,
Afonine Pavel,
Dauter Miroslawa,
Dauter Zbigniew
Publication year - 2010
Publication title -
acta crystallographica section c
Language(s) - English
Resource type - Journals
eISSN - 1600-5759
pISSN - 0108-2701
DOI - 10.1107/s0108270110044136
Subject(s) - chemistry , hydrogen bond , amide , crystallography , covalent bond , stereochemistry , molecule , organic chemistry
The title compound, C 23 H 26 F 2 N 2 O 4 , 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 .