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Therefore, it may be concluded that 479 cm−1 is the Zn–O bond frequency.
The broad band at 3,298 cm−1 in Figure 7a is characteristic for the N-H stretching bond frequency of primary and secondary amine groups, and it has shifted to 3,281 cm−1 in Figure 7b.
Increased internal hydrogen bond frequency showed a high degree of accordance with enhanced inhibition in vitro.
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The amide I′ band (1710 1600 cm–1) is composed primarily of peptide bond frequencies [ν(C=O)] that are sensitive to conformational changes within proteins.
In Figure 11(a), the H-bond frequency is greater than in other compounds, indicating that Labiatic acid may have a higher activity in this protein.
The separation between the bonded and de-bonded frequency bands averaged approximately 300 Hz, indicated by ΔF Σ in Fig. 7.
Several peptide sequences were preselected based on intermolecular H-bond frequencies.
Subsite binding energies were predicted with r2 = 0.502 correlation coefficient, while bond cleavage frequency prediction resulted in r2 = 0.538.
Differences in bond failure frequency in groups A and B were analysed using a Fisher exact test.
Unlike the work of Lucovsky et al. [67] who reported the Si F stretching mode frequencies around 935 cm−1 and Si F bond bending frequencies below 400 cm−1, we observed weak shoulder peaks of Si F bond with fundamental frequencies in the range 763 772 cm−1 (Fig. 6c).
Calculations for training set resulted in good correlation in case of subsite binding energies (r2 = 0.827 0.929) and bond cleavage frequencies (r2 = 0.727 0.835).
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