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Two new series of allocolchicinoids mimicking the structure of -N-acetylcolchinol O-mether ether (2, NCME) were synthesized and evaluated for their abilities to inhibit tubulin assembly.
In this study, three siRNAs (ps-PA496, ps-PA1116, and ps-PA1473) thegeting the polymerase A (PA) gene of highly pathogenic avian influenza virus (HPAIV) H5N1 were designed and evaluated for their abilities to inhibit HPAIV replication.
All extracts were evaluated for their abilities to scavenge free radicals (DPPH method) and inhibition of the oxidation of linoleic acid (β-carotene/linoleic acid) in vitro test systems.
Such cells were functionally evaluated for their abilities to multi-lineage reconstitute myeloablated hosts.
These primary fibroblasts were grown to 100% confluent in culture and then evaluated for their abilities to promote cancer cells to form colony in soft agar.
Antioxidant properties of the crude extracts and different fractions of the six plants were evaluated for their abilities to scavenge 2,2-diphenyl-2-picrylhydrazyl hydrate (DPPH), nitric oxide (NO) and superoxide anion (SO) radicals in vitro.
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Several other herbs and supplements have been evaluated for their ability to reduce inflammation in people with rheumatoid arthritis.
These compounds were evaluated for their ability to in vitro inhibit VEGFR2 kinase enzyme.
Additionally, SCIs were evaluated for their ability to serve as indicators of effluent dispersion.
Several model mechanism-based inhibitors (MbIs) were designed and evaluated for their ability to inhibit sulfatases.
A series of N-benzoylindazoles was synthesized and evaluated for their ability to inhibit HNE.
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