Search results for " Enzyme catalysis"

showing 2 items of 2 documents

1,2,3-Triazole in Heterocyclic Compounds, Endowed with Biological Activity, through 1,3-Dipolar Cycloadditions

2014

1,3-Dipolar cycloaddition reactions can be considered a powerful synthetic tool in the building of heterocyclic rings, with applications in different fields. In this review we focus on the synthesis of biologically active compounds possessing the 1,2,3-triazole core through 1,3-dipolar cycloaddition reactions. The 1,2,3-triazole skeleton can be present as a single disubstituted ring, as a linker between two molecules, or embedded in a polyheterocycle. The cycloaddition reactions are usually catalysed by copper or ruthenium. Domino reactions can be achieved through dipolarophile anion formation, generally followed by cyclisation. The variety of attainable heterocyclic structures gives an ill…

Cycloaddition / Nitrogen heterocycles / Domino reactions / Homogeneous catalysis / Enzyme catalysis / Biological activity / Medicinal chemistrySettore CHIM/03 - Chimica Generale E InorganicaCycloaddition Nitrogen heterocycles Domino reactions Homogeneous catalysis Enzyme catalysis Biological activity Medicinal chemistrySettore CHIM/08 - Chimica Farmaceutica
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Resveratrol-Related Dehydrodimers: Laccase-Mediated Biomimetic Synthesis and Antiproliferative Activity

2012

Seven resveratrol-related monomeric stilbenoids were submitted to biomimetic oxidative coupling in the presence of laccase from Trametes versicolor (TvL), and gave racemic dihydrobenzofuran dehydrodimers (±)-15 to (±)-21. These products, after spectral characterization, were submitted to an antiproliferative activity bioassay against SW480 human colon cancer cells. Five racemates were found to be active, and were resolved by chiral HPLC. The pure enantiomers were subjected to circular dichroism measurements to establish their absolute configurations at C-7 and C-8. These enantiomerically pure compounds were submitted to the antiproliferative activity assay towards SW480 cells, and were all …

LaccaseCircular dichroismAntitumor agentsbiologyStereochemistryChemistryOrganic ChemistryMedicinal chemistryEnzyme catalysisStructure-activity relationshipsAntiproliferationMedicinal chemistry; Biomimetic synthesis; Enzyme catalysis; Antiproliferation; Antitumor agents; Structure-activity relationshipsbiology.organism_classificationStereocenterEnzyme catalysisChiral column chromatographyBiomimetic synthesisBiomimetic synthesisPhysical and Theoretical ChemistryEnantiomerTrametes versicolorEuropean Journal of Organic Chemistry
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