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Download analogous structures
Download analogous structures







download analogous structures

This review summarizes and discusses important developments and achievements in stimuli-responsive membranes.

download analogous structures

Further conferring membranes with stimuli responsiveness can allow them to dynamically tune their pore structure and/or surface properties for efficient separation performance.

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Although some differences in the biological activity of the complexes were found, it can be concluded that both complexes target the inflammatory processes on a cellular level.Membranes have been extensively studied and applied in various fields owing to their high energy efficiency and small environmental impact. The impact of the complexes on the expression of selected genes in the tested cell lines was further investigated by qRT-PCR methods and their DNA binding properties towards the isolated genomic DNA samples were evaluated by competitive binding studies with ethidium bromide. The complexes were most active against the 12Z among the studied cell lines, while the flufenamato complex, which showed an IC 50 value around 2 μM, was able to effectively trigger apoptosis through the caspase pathway. The cytotoxic effects of the complexes were studied on three selected cell lines, including epithelial hTERT HME1 used as a healthy control, endometriotic 12Z and endometrial cancer SK-UT-1. Both complexes create an interesting structural motif resembling molecular tweezers, with an open cavity between the fenamato and flufenamato ligands, and exhibit moderate radical scavenging activity, with the fenamato complex being more active. Their molecular structure was determined by the single-crystal X-ray diffraction method, which revealed that the complexes are isostructural and form analogous molecules and. Two novel Mn( II) complexes with non-steroidal anti-inflammatory drugs, fenamic (Hfen = 2-(phenylamino)benzoic acid) and flufenamic acid (Hflu = N-(3-trifluoromethylphenyl)-2-aminobenzoic acid) and neocuproine (neo) as a supporting ligand were designed, synthesized and characterized.









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