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Inspection of these individual compounds revealed two explanations.
Moreover, quite often the same compounds revealed promising and somewhat unexpected plant growth regulatory activity.
Moreover, most of the tested compounds revealed good gastrointestinal safety profile.
Some of the prepared compounds revealed good activity against the urease splitting bacteria, Proteus mirabilis.
Binding affinity results of the prepared compounds revealed good binding affinities at both melatonin receptor subtypes.
Overall, the designed compounds revealed good, in vivo, antinociceptive activity and satisfactory anti-inflammatory profile.
The new compounds revealed excellent in vitro antifungal activity with broad spectrum.
All these compounds revealed MIC values in the range of 15.0 78.6 μM.
Biological investigation of the four compounds revealed that they all inhibit the growth of P. falciparum.
Moreover, the dicationic compounds revealed a significantly lower toxicity than the monocationic counterparts.
These compounds revealed significant DPPH scavenging potential exhibiting IC50 values of 4.12, 5.06, 6.08 and 7.17 μg/mL, respectively [54].
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