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Surface enrichment of corrosion resistant compounds was shown by XPS.
A significant correlation between experimental activity [Log(1/IC50)] and the corresponding binding free energy (ΔGb) of the docked compounds was shown.
The highest affinity among all compounds was shown by 1- 6- 3-phenylphenoxy)hexyl)azepane (1- 6- 3-phenylphenoxyf 1- 6- 3-phenylphenoxy
The regression coefficient (R2) of pure compounds was shown at 0.9992, 0.9993 and 0.9979.
Previously, the biosynthesis of these compounds was shown to be regulated by transcription factors MYB28 and MYB29.
Sensitivity to certain compounds was shown to be treatment-dependent.
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The structures of these two compounds are shown below.
These compounds were shown to have high affinity for the 5-HT6 receptor.
These compounds were shown to inhibit the proliferation of U87MG cells in the low micromolar range.
The structures of these compounds are shown in Table 8.
The synthesized trisubstituted triazine compounds are shown in Table 3.
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