about
Synthesis and pharmacological screening of a large library of 1,3,4-thiadiazolines as innovative therapeutic tools for the treatment of prostate cancer and melanoma.A novel library of saccharin and acesulfame derivatives as potent and selective inhibitors of carbonic anhydrase IX and XII isoforms.The sodium salt of the enantiomers of ricobendazole: Preparation, solubility and chiroptical properties.Open saccharin-based secondary sulfonamides as potent and selective inhibitors of cancer-related carbonic anhydrase IX and XII isoforms.Analysis of imidazoles and triazoles in biological samples after MicroExtraction by packed sorbent.Synthesis and biological evaluation of anti-Toxoplasma gondii activity of a novel scaffold of thiazolidinone derivatives.Enantiomers of triclabendazole sulfoxide: Analytical and semipreparative HPLC separation, absolute configuration assignment, and transformation into sodium salt.Protective Effects Induced by Microwave-Assisted Aqueous Harpagophytum Extract on Rat Cortex Synaptosomes Challenged with Amyloid β-Peptide.Magnetic Metal-Organic Framework Composite by Fast and Facile Mechanochemical Process.Design, synthesis and biochemical evaluation of novel multi-target inhibitors as potential anti-Parkinson agents.Inhibition of Human Monoamine Oxidase: Biological and Molecular Modeling Studies on Selected Natural Flavonoids.Crystal structure of the Eg5 - K858 complex and implications for structure-based design of thiadiazole-containing inhibitors4-(3-Nitrophenyl)thiazol-2-ylhydrazone derivatives as antioxidants and selective hMAO-B inhibitors: synthesis, biological activity and computational analysisDesign, Synthesis, Docking Studies and Monoamine Oxidase Inhibition of a Small Library of 1-acetyl- and 1-thiocarbamoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazolesThe Up-Regulation of Oxidative Stress as a Potential Mechanism of Novel MAO-B Inhibitors for Glioblastoma TreatmentNovel therapies for glaucoma: a patent review (2013-2019)Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffoldBenzo[b]tiophen-3-ol derivatives as effective inhibitors of human monoamine oxidase: design, synthesis, and biological activity
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0001-5701-6925
@en
name
Paolo Guglielmi
@ast
Paolo Guglielmi
@en
Paolo Guglielmi
@es
Paolo Guglielmi
@nl
type
label
Paolo Guglielmi
@ast
Paolo Guglielmi
@en
Paolo Guglielmi
@es
Paolo Guglielmi
@nl
prefLabel
Paolo Guglielmi
@ast
Paolo Guglielmi
@en
Paolo Guglielmi
@es
Paolo Guglielmi
@nl
P106
P1153
7003900564
P31
P496
0000-0001-5701-6925