Beilstein J. Org. Chem.2015,11, 2105–2116, doi:10.3762/bjoc.11.227
calculate the properties of the hydrogen bond critical point.
The compounds used in this study and their atom numbering.
Possible conformations of 1.
Driving forces influencing association exemplified on two "extreme" conformations of 1∙∙∙benzoate.
Two possible, extreme multiple hydrogen bonded multimeric
structures of 1 and VT 1H NMR spectra (from +25 to −40 °C, low temperatures at bottom, CDCl3).
The proposed structure explaining unusual behavior of the titration curve for 1∙∙∙9 titration and anisotropy influence on methylene chemical shift.
Collective titration curves (H1/H7 and H3/H5 chemical shifts
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Graphical Abstract
Figure 1:
The compounds used in this study and their atom numbering.
Beilstein J. Org. Chem.2012,8, 2106–2117, doi:10.3762/bjoc.8.237
- to 8-fold more active than the monomeric peptide against the phytopathogenic bacteria. These results suggest that preassembling antimicrobial peptides to multimericstructures is not always associated with a significant improvement of the activity. In contrast, the carbopeptides synthesized were
active against human red blood cells pointing out that peptide preassembly is critical for the hemolytic activity. Notably, peptide preassembly resulted in an enhanced bactericidal effect.
Keywords: antimicrobial activity; carbopeptides; multimericstructures; oxime ligation; phytopathogenic bacteria
multivalent compounds exhibited low MIC values against plant and human pathogenic bacteria, a significant multimeric effect was not observed. Our results support the notion that preassembly of antimicrobial peptides to multimericstructures prior to contact with the microbial surface does not necessarily lead