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The structure of the bromo-substituted compound is confirmed by single crystal XRD study.
The nature of the recognition process is evaluated by UV-Vis, ATR-IR and potentiometry, while the purity of the compound is confirmed by LC-MS and cyclic voltammetry.
If inhibitory activity of compound is confirmed in experimental tests, it serves as a basis for design of new patented inhibitors.
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The identity and chemical purity of this compound were confirmed by 1H NMR, mass spectroscopy, HPLC analysis, and elemental analysis.
The functional group of synthesized compound was confirmed by Fourier transform infrared (FT-IR) spectroscopy (Perkin Elmer, UK).
The purity (>95%) of the compound was confirmed by analytical HPLC on a C18 column.
The activity of each compound was confirmed in repeat assays using either the Bodipy-C16 or PED-6 lipid.
In addition, the binding mode of one compound was confirmed using X-ray crystallography.
The relative and absolute stereochemistry of this compound was confirmed by X-ray crystallography (Scheme 23).
The structure of this compound was confirmed by NMR (Fig. S2B, S3, S4 Supplementary Materials).
The identity of isolated compound was confirmed by LC-MS and was found to be >98% pure.
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