about
Effect of cooking method on carnosine and its homologues, pentosidine and thiobarbituric acid-reactive substance contents in beef and turkey meat.New 1,4-dihydropyridines endowed with NO-donor and calcium channel agonist properties.Multivariate analysis applied to Raman mapping of dye-functionalized carbon nanotubes: a novel approach to support the rational design of functional nanostructures.Synthesis and voltage-clamp studies of methyl 1,4-dihydro-2, 6-dimethyl-5-nitro-4-(benzofurazanyl)pyridine-3-carboxylate racemates and enantiomers and of their benzofuroxanyl analogues.Profile of the intermolecular forces governing the interaction of drugs with mucin.Microwave-assisted Maillard reactions for the preparation of advanced glycation end products (AGEs).A sensitive and practical fluorimetric test for CNT acidic site determination.Studies on agents with mixed NO-dependent and calcium channel antagonistic vasodilating activities.Searching for balanced hybrid NO-donor 1,4-dihydropyridines with basic properties.Platelet antiaggregatory effects and haemodynamic activity of two terfuroxan isomer pairs.New 1,4-dihydropyridines conjugated to furoxanyl moieties, endowed with both nitric oxide-like and calcium channel antagonist vasodilator activities.Determination of carnosine, anserine, homocarnosine, pentosidine and thiobarbituric acid reactive substances contents in meat from different animal species.Thermolysis of 4-(2-azido-3-nitrophenyl)-1,4-dihydropyridines as source of β-carboline derivatives and some related compoundsMucin–drugs interaction: The case of theophylline, prednisolone and cephalexinThe different kinetic behavior of two potential photosensitizers for PDTA transient kinetic study between signaling proteins: the case of the MEK–ERK interactionEffect of dietary supplementation of vitamin E in pigs to prevent the formation of carcinogenic substances in meat productsFunctionalization of Single-Walled Carbon Nanotubes through 1,3-Cycloaddition of Carbonyl Ylides under Microwave IrradiationLigand-based design, in silico ADME-Tox filtering, synthesis and biological evaluation to discover new soluble 1,4-DHP-based CFTR activatorsGRIND-based 3D-QSAR and CoMFA to investigate topics dominated by hydrophobic interactions: The case of hERG K+ channel blockersSquaraine Dyes: Interaction with Bovine Serum Albumin to Investigate Supramolecular Adducts with Aggregation‐Induced Emission (AIE) PropertiesResolution of some 4-benzofurazanyl and 4-benzofuroxanyl 1, 4-dihydropyridine derivatives by chiral HPLC on whelk-o1 and some polysaccharide chiral stationary phasesDisassembling the complexity of mucus barriers to develop a fast screening tool for early drug discovery
P50
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P50
description
researcher ORCID ID = 0000-0001-7262-6166
@en
wetenschapper
@nl
name
Sonja Visentin
@ast
Sonja Visentin
@en
Sonja Visentin
@es
Sonja Visentin
@nl
type
label
Sonja Visentin
@ast
Sonja Visentin
@en
Sonja Visentin
@es
Sonja Visentin
@nl
prefLabel
Sonja Visentin
@ast
Sonja Visentin
@en
Sonja Visentin
@es
Sonja Visentin
@nl
P1153
7004184798
P21
P31
P496
0000-0001-7262-6166