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The biological and computational results of these new molecules were compared with 1-hydroxyacridones.
Therefore, the two molecules were compared within 6 hours of incubation with Salmonella and E. coli biofilms.
The obtained HSA binding of known drug molecules were compared to the Immobilizd Artificial Membrane binding data (CHI IAM) obtained by our previously described HPLC‐based method.
The experimental IC50 activity values of these molecules were compared with its corresponding predicted C-Docker energy values and the point plot is graphed to identify the correlation between the IC50 and C-Docker energy.
The molecular orbital energy levels, the molecular orbital spatial distributions and the electronic absorption spectra of the ZnPcB series molecules were compared with those of TT7 and TT8 to reveal the substituent effects of different donor and acceptor groups on the phthalocyanine compounds and select good sesitizer candidates.
Different growth factors and molecules were compared.
Similar(46)
In those strains, the distribution of the intracellular concentrations of the three storage molecules was compared (Fig. 5).
The equilibrium properties of the different disubstituted polyacetylenes molecules are compared on the base of the normalised scaling plots.
While the calculation of the MCS values was quite demanding, the calculation of other similarities (see "Methods" section) was much simpler, as those used depended only on the number of heavy atoms in the molecules being compared and those in their MCS.
Thus, the relative extent of activation of key signaling molecules was compared between each cell type.
The mRNA expression of these molecules was compared between the two sample groups of GC- and GC+ by real-time PCR.
More suggestions(15)
molecules were collected
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molecules were represented
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molecules were increased
molecules were discovered
molecules were visualized
molecules were localized
molecules were deposited
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