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Deltamethrin, a widely used type II pyrethroid insecticide, is a relatively potent neurotoxicant.
In vitro studies indicated that most of these compounds are relatively potent inhibitors of each enzyme.
Third, this interaction should be achieved at low concentrations, meaning that the substance has to be relatively potent.
Several human monoclonal antibodies (hmAbs) including b12, 2G12, and 2F5 exhibit relatively potent and broad HIV-1-neutralizing activity.
Glycosylation and hydroxyl substituents of anthocyanin had lower affinity to HSA at pH 4, but had relatively potent binding at pH 7.4.
Nonetheless they concluded that N. sativa has relatively potent bronchodilatory effects but when given orally it is less effective than conventional bronchodilators.
Two of them, compounds 17f and 17k, displayed relatively potent antagonist effects on glucagon receptors with IC50 values of 3.9 and 3.6 μM, respectively.
Some of the compounds were found to be substrates of PSAO and relatively potent inhibitors of MPAO (and vice versa) all at once.
We identified SLIARK-NH2 and SL-Cha-ARL-NH2 as relatively potent, highly selective PAR-2 agonists with EC50 values of 4 μM.
Few compounds were significantly active against Escherichia coli and Proteus vulgaris with MIC less than 0.06 μg/ml and relatively potent than ciprofloxacin.
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Most of synthesized compounds were relatively more potent to celecoxib (0.78 μM), diclofenac (2.94 μM) and indomethacin (7.24 μM).
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