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Beilstein J. Org. Chem. 2022, 18, 1–12, doi:10.3762/bjoc.18.1
Graphical Abstract
Scheme 1: Synthesis of SMC stapled axin CBD peptides. Reaction conditions: (a) Pd2(dba)3, sSPhos, KF, DME/EtO...
Scheme 2: Overview of the different cross-linkages obtained by intramolecular SMC. A) General structure of SM...
Figure 1: Analysis of the secondary structure by circular dichroism: CD spectra of both isomers of stapled pe...
Figure 2: In vitro binding affinities to β-catenin determined by competitive fluorescence polarisation assays....
Figure 3: Cleavage sites of Proteinase K digestion indicated by a red arrow.
Figure 4: Principal component analysis (PCA) of the macrocycle’s non-hydrogen atoms in the two isomers of P5....
Figure 5: Molecular modelling of the conformational preferences of the SMC stapled peptides P5 (with cis or t...
Beilstein J. Org. Chem. 2019, 15, 1581–1591, doi:10.3762/bjoc.15.162
Figure 1: Glycosylated building blocks prepared for solid phase peptide synthesis (SPPS).
Scheme 1: A) Modification of Fmoc-Sieber-PS resin: a. piperidine in DMF (20% v/v), rt; 3 × 10 min; b. o-NBS-C...
Figure 2: Model AFGP analogues.
Figure 3: Conformational preferences of investigated glycopeptides.
Figure 4: Conformational preferences of monosaccharide moiety. A) cluster 1 for glycopeptide 3, B) cluster 1 ...
Beilstein J. Org. Chem. 2014, 10, 660–666, doi:10.3762/bjoc.10.58
Figure 1: Sequences of the investigated dehydropeptides.
Figure 2: The most stable conformation of peptide 1 proposed based on XPLOR-NIH calculations. Conformation 1a...
Figure 3: Proposal of the most stable conformation of peptide 2 based on XPLOR-NIH calculation. Conformation ...
Figure 4: Proposal of the most stable conformation of peptide 3 based on XPLOR-NIH calculations.