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Both compounds were not cytotoxic in uninfected BHK cells at concentrations of 1 mM.
Both compounds were not toxic at relevant levels (Table 1).
Similar(58)
However, the effect of both compounds was not only exerted on the enzyme Vmax, but they also decreased values of S0.5 for substrates.
Both the compounds were not toxic to normal breast epithelial cell line (MCF10A), as there was no growth inhibition up to a concentration of 30 μM.
After treatment, the peak was still present in the samples obtained from both reactors, which indicated protein like compounds were not degraded.
3DEEM fluorescence analysis shows that protein like compounds were not degraded in both AnSBR-Fe and AnSBR-C.
Hence both were selected as a ligand for molecular docking studies as remaining compounds were not of any therapeutic significance.
These compounds were not associated with fibrosis.
Kinetic models for hydrocracking of model compounds were not analyzed.
However, these compounds were not always detected in samples [55].
The entire process time was less than 2 h, and toxic compounds were not used.
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