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Compounds were screened in quadruplicate on three separate occasions.
Compounds were screened for their antibacterial activity.
Compounds were screened in triplicate at a final concentration of 10 µM.
Thus, twelve target compounds were screened out and synthesized.
These compounds were screened for their α-glucosidase activity.
These compounds were screened for anticancer and antimicrobial activity.
Additionally, all the compounds were screened for anti-tuberculosis activity.
The resulting compounds were screened in vitro for pancreatic lipase (PL) inhibitory activity.
The compounds were screened using recombinant T. cruzi (Tulahuen strain) expressing beta-galactosidase.
The compounds were screened for antioxidant activities in human blood under oxidation stress conditions.
Compounds were screened against ciprofloxacin resistant bacteria and Mycobacterium tuberculosis H37Rv species.
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