Sentence examples for strong antagonistic from inspiring English sources

Exact(42)

Moreover, strain AR6 exhibited strong antagonistic activity against phytopathogen Aspergillus niger.

The present evaluation clearly indicated that T. harzianum had strong antagonistic activity against P. ultimum than against P. capsici.

Hydroxysafflor yellow A has also been demonstrated with a strong antagonistic effect on platelet activating factor receptor [26].

A series of 1-Sulfonyl-6-Piperazinyl-7-Azaindoles 1-Sulfonyl-6-Piperazinyl-7-Azaindoles 1-Sulfonyl-6-Piperazinyl-7-Azaindoles 1-Sulfonyl-6-Piperazinyl-7-Azaindoles 1-Sulfonyl-6-Piperazinyl-7-Azaindoles 1-Sulfonyl-6-Piperazinyl-7-Azaindoles

Tissue functional assay in vitro showed that compound 2 exerted strong antagonistic activity on α1B-AR (pA2 7.13) with a poor selectivity for α1A and α1D subtypes.

Compounds 9, 12, 13, 15, 17, 18, 21, 22, 25 and 26 exerted strong antagonistic effects on α1A and/or α1D subtypes over α1B in vitro.

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Similar(16)

suggests that the former is only a moderate mycoparasite with significant variation among isolates, whereas the latter species may exhibit a stronger antagonistic potential against all epigeal fungi tested (Fig. 7).

The strongest antagonistic effect was found at 500 nM, and the differences in concomitant treatment effects caused by the tamoxifen concentration were similar to those for MAPT expression.

The hemizygosity of the X chromosome, X-autosomal interaction, the higher proportion of X-linked miRNAs in testis, and stronger antagonistic and/or adaptive sexual selection in the male, can all collectively drive evolution of testis miRNAs that are X-linked, at a faster rate than those that are autosomal.

On the basis of comprehensive evaluations, compound 8d which showed strong TRPV1 antagonistic activity, middle COX-2 inhibition, weak ulcerogenic action and had no hyperthermia side-effect was considered as a safe candidate for the further development of analgesic drugs.

These results indicated that most functional groups of 1a were conserved, and six new compounds (1b, 1c, and 9a d) exhibited strong PPARγ antagonistic activities (IC50 values of 5.2 25.8 μM) against 10 μM rosiglitazone in the promotion of the PPARγ LBD CBP (ligand-binding domain and cAMP-response-element binding protein) interaction as investigated by yeast two-hybrid technology based assay.

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