Two novel zinc(II) coordination polymers constructed from in situ amidation ligands
Sign Up to like & getrecommendations! Published in 2018 at "Journal of Molecular Structure"
DOI: 10.1016/j.molstruc.2017.12.100
Abstract: Abstract Two novel coordination compounds, [Zn(Hbimh) (H2O)]·H2O (1) and [Zn(Hbimh)]·(4,4ʹ-bpy)0.5 (2) (H3bimh = benzimidazole-5,6-hydrazide, 4,4ʹ-bpy = 4,4ʹ-bipyridine), have been prepared from the hydrothermal in situ amidation cyclization reactions of H3bimdc (H3bimdc = benzimidazole-5,6-dicarboxylic acid) and hydrazine hydrate (N2H4·H2O). Compound 1 exhibits… read more here.
Keywords: novel zinc; two novel; zinc coordination; situ amidation ... See more keywords
Highly selective capture of minicircle DNA biopharmaceuticals by a novel zinc-histidine peptide conjugate
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DOI: 10.1016/j.seppur.2016.10.054
Abstract: Abstract The use of minicircle DNA (mcDNA) biomolecules as a pharmaceutical product holds remarkable potential due to their improved therapeutic efficacy in comparison with standard non-viral gene expression vectors. However, mcDNA translation into clinical application… read more here.
Keywords: histidine; minicircle dna; novel zinc; dna biopharmaceuticals ... See more keywords
Design, Synthesis, and Docking Study of Acyl Thiourea Derivatives as Possible Histone Deacetylase Inhibitors with a Novel Zinc Binding Group
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DOI: 10.3390/scipharm87040028
Abstract: Histone deacetylase inhibitors with zinc binding groups often exhibit drawbacks like non-selectivity or toxic effects. Thus, there are continuous efforts to modify the currently available inhibitors or to discover new derivatives to overcome these problems.… read more here.
Keywords: novel zinc; deacetylase inhibitors; histone deacetylase; histone ... See more keywords