Sentence examples for exhibited signals from inspiring English sources

1H-NMR spectrum of compound 4 exhibited signals at 10.2, 11.4 attributed to 2NH groups and 13.1 ppm assigned to OH group which exchangeable with D2O.

In addition, the 1H NMR also exhibited signals due to one β-glucopyranosyl unit [δ 5.08 (d, J = 7.0 Hz, H-1")].

The 1H and 13C NMR spectra exhibited signals which ascribable to three methyls, four methylenes (one oxygenated), four methines (two oxygenated), and four quaternary carbons (a tetrasubstituted double bond, a carbonyl).

The later compound was also confirmed by 1H-NMR spectrum exhibited signals at δ 1.20, 1.90, and 3.90, due to CH3, CH2, and CH pyrrole protons respectively, in addition to an aromatic multiplet in the region of δ 7.53 7.57.

Thus, compound 2 was elucidated as shown in Fig. 1, and was given the trivial name vibralactone T. The 13C NMR and DEPT spectra (Tables 1 and 2) of the colorless oil compound 3 exhibited signals ascribable to three methyls, three methylenes, four methines, and five quaternary carbons (two carbonyls).

1H-NMR of 22 exhibited signals at 3.4 ppm corresponding to N-CH3 group, 5.9 ppm due to NH2 group, two doublet at 6.1, 7.4 ppm for 2 CH quinoline, two doublet at 6.5, 6.6 ppm assigned to CH = CH groups, singlet at 12.0 NH. 13C-NMR of 22 showed singlet at 186.6 ppm attributed to (CO) group.

The one in the diagram exhibited signaling that makes defense more accurate.

Two-dimensional 1H,15N-NMR experiments exhibited signal loss upon complexation consistent with the formation of high-molecular-weight species.

The −60 sentinel was weak elsewhere whereas the −228 sentinel exhibited signal in the limb buds (Fig. 6B).

A number of clusters with unknown functions were identified as coding sequences which exhibited signal peptides, such as clusters 11 and 126.

Each individual patient exhibited signal changes in those left and right hippocampal areas that reached significance in group statistics (Fig. 4).