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The Z-propenones were also found to be more potent and selective than their E-isomers for COX-2 inhibitory activity.
The inhibitory activity of acetone extracts was found to be more potent and similar when compared to the positive control acarbose.
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Among the tested compounds, quinazolines 1 and 3 were found to be more potent than the standard drug Vinblastine against HepG2 and MCF-7 cell lines.
The isolated compounds (1 4) were screened for AChE enzyme inhibition assay in which compound 3 and 4 were found to be more potent AChE inhibitor.
Among the plants used, T. ammi and C. nocturnum were found to be more potent than the others.
Furthermore, the compounds with either bromide anion or N-methylene phenyl and N-heptyl substitutions found to be more potent cytotoxic.
Organic extracts of B9_Pink and CK01 isolates were found to be more potent than streptomycin against S. typhimurium.
The Organic extract of B9_Pink and B19 were also found to be more potent than streptomycin against E. coli.
Further, dimethyl substituted compound (8o) found to be more potent as compared to the single methoxy substituted compounds (8a, 8b and 8c).
G2 was found to be more potent than F1.
Nearly all tested compounds were found to be more potent against Candida albicans than control drug fluconazole.
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