Sentence examples for potent table from inspiring English sources

LXY30 was found to be most potent (Table 2).

Acetone extracts were found to retard growth of both fungi tested to a similar extent as the ethanol extracts (Table 4) although they comprised only roughly half the weight (Table 3) so were roughly twice as potent (Table 4).

All other types of inhibitors were found to be one to two orders of magnitude less potent (Table 3).

The dansyl equivalent of ABEA-X-BY630, AUEA-dansyl (10), did show measurable affinity for the A1 receptor, but was significantly less potent (Table 2).

Compound (R)- 5, which has a 3,4-dihydro-2 H-benzo[ b][1,4]oxazine side chain, also displays enhanced CREBBP affinity, whereas the two fluorine-containing derivatives (R)- 7 and (R)- 8 as well as (S)- 1 were less potent (Table 1).

Cytotoxic studies against A549 lung adenocarcinoma cancer cell line showed Vasicine acetate to be the most potent compound (Table 4).

An analogue of cNPF1Flu with an acetyl group in place of the dye was also tested and showed 2-fold less potent inhibition (Table 2).

Partial atomic charges of +0.3 at ammonium hydrogen atoms and −0.5 to −0.6 on carboxylate oxygen atoms were common among the most potent ligands (Table 2).

The ten most potent compounds (Table 7) display selective high inhibitory activity against 11β-HSD1, wIC50IC50 values below 50 n m, when evaluated on a stably transfected HEK293 cell line.

We conclude that omega-9 cis unsaturated fatty acids between 18 and 22 carbons specifically inhibit MSI1 RNA-binding activity and identify erucic acid as the most potent inhibitor (Table 1).

We examined the structure activity relationship of SKI-356313 through a limited focused library of 14 derivatives, based on the 2-phenyl-1H indole core scaffold substituted at positions 1- and 6- on the indole and position 3- on the phenyl as an avenue in the search of more potent compounds (Table 1).