Sentence examples for moderate inhibitory potency from inspiring English sources

Both of these chemical classes displayed moderate inhibitory potency against SUMO E1.

The results showed some 4,5,6,7-tetrahydro-2-[[ phenylamino thioxomethyl]amino]-benzo[b]thiophene-3-carboxylic acid derivatives (3a–i) exhibited moderate inhibitory potency on diphenolase activity of tyrosinase.

The results showed that the synthetic compounds possessed good to moderate cholinesterases inhibitory potency.

Most of them exhibited potent AChE inhibitory activity, high selectivity for AChE over BuChE, and moderate to good inhibitory potency toward Aβ aggregation.

The remaining isomeric iodo compounds that have low to moderate COX-2 inhibitory potency and selectivity in the purified COX enzyme assay were not tested for their inhibitory activity against COX-2 enzyme in the activated intact RAW264.7 cell line assay.

Among them, compound 49 displayed excellent inhibitory potency toward acetylcholinesterase (AChE), moderate anti-oxidative activity, selective biometal chelating, and possessed good inhibitory effects on self-induced and Cu2+-induced Aβ aggregation.

All the compounds showed inhibitory potencies, and 10 of these exhibited moderate inhibitory activities with IC50 values less than 10 μM.

Whereas 17a maintained moderate potency against EML4-ALK-Ba/F3 cell (IC50 = 0.61 μM), the others lost ALK inhibitory potency substantially (Table 1).

A six-fold difference of the inhibitory potency of paraoxon with human and guinea pig AChE was recorded while only moderate differences of the reactivation constants between human and animal AChE were determined.

Generally speaking, the inhibitory potency of all compounds in the series against the parasites did not strongly correlate with inhibitory potency against falcipain-2 for selected compounds tested, which at best was weak to moderate, suggesting other mechanisms of inhibition may also be involved or compounds may be selectively taken up by Plasmodium falciparum.

Increasing the dose of CN boosted its inhibitory potency.