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Kinetic Study on the Base-Catalyzed Imine-Enamine Tautomerism of a Chiral Biologically Active Isoxazoline Derivative by HPLC on Amylose Tris(3,5-dimethylphenylcarbamate) Chiral Stationary Phase

Molecules (Basel, Switzerland), 2023-09, Vol.28 (18), p.6518

2023

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Selective MAO-B inhibitors: a lesson from natural products

Molecular diversity, 2014-02, Vol.18 (1), p.219-243

2014

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Chiral Hydroxy Metabolite of Mebendazole: Analytical and Semi-Preparative High-Performance Liquid Chromatography Resolution and Chiroptical Properties

Pharmaceuticals (Basel, Switzerland), 2024-05, Vol.17 (6), p.696

2024

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Novel Insights on Human Carbonic Anhydrase Inhibitors Based on Coumalic Acid: Design, Synthesis, Molecular Modeling Investigation, and Biological Studies

International journal of molecular sciences, 2022-07, Vol.23 (14), p.7950

2022

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Synthesis and Evaluation of Thymol-Based Synthetic Derivatives as Dual-Action Inhibitors against Different Strains of H. pylori and AGS Cell Line

Molecules (Basel, Switzerland), 2021-03, Vol.26 (7), p.1829

2021

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4-(3-Nitrophenyl)thiazol-2-ylhydrazone derivatives as antioxidants and selective hMAO-B inhibitors: synthesis, biological activity and computational analysis

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.597-612

2019

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Open saccharin-based secondary sulfonamides as potent and selective inhibitors of cancer-related carbonic anhydrase IX and XII isoforms

Journal of enzyme inhibition and medicinal chemistry, 2017-12, Vol.32 (1), p.51-59

2017

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Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives

Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.685-692

2021

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Design, Synthesis, Docking Studies and Monoamine Oxidase Inhibition of a Small Library of 1-acetyl- and 1-thiocarbamoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazoles

Molecules (Basel, Switzerland), 2019-01, Vol.24 (3), p.484

2019

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Synthesis, Molecular Modeling, and Selective Inhibitory Activity against Human Monoamine Oxidases of 3-Carboxamido-7-Substituted Coumarins

Journal of medicinal chemistry, 2009-04, Vol.52 (7), p.1935-1942

2009

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2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2270183-2270183

2023

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Synthesis, selective anti-Helicobacter pylori activity, and cytotoxicity of novel N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides

Bioorganic & medicinal chemistry letters, 2010-08, Vol.20 (16), p.4922-4926

2010

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Neem oil nanoemulsions: characterisation and antioxidant activity

Journal of enzyme inhibition and medicinal chemistry, 2017-01, Vol.32 (1), p.1265-1273

2017

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Meet Our Editorial Board Member

Anti-cancer agents in medicinal chemistry, 2020-11, Vol.20 (18), p.2137-2137

Secci, Daniela

2020

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Exploring New Scaffolds for the Dual Inhibition of HIV-1 RT Polymerase and Ribonuclease Associated Functions

Molecules (Basel, Switzerland), 2021-06, Vol.26 (13), p.3821

2021

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Synthesis and Biological Evaluation of Carvacrol-Based Derivatives as Dual Inhibitors of H. pylori Strains and AGS Cell Proliferation

Pharmaceuticals (Basel, Switzerland), 2020-11, Vol.13 (11), p.405

2020

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Discovery and optimization of pyrazoline derivatives as promising monoamine oxidase inhibitors

Current topics in medicinal chemistry, 2012-10, Vol.12 (20), p.2240-2257

2012

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Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.1400-1413

2019

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Novel insights on saccharin- and acesulfame-based carbonic anhydrase inhibitors: design, synthesis, modelling investigations and biological activity evaluation

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.1891-1905

2020

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Atriplex mollis Desf. Aerial Parts: Extraction Procedures, Secondary Metabolites and Color Analysis

Molecules (Basel, Switzerland), 2018-08, Vol.23 (8), p.1962

2018

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Benzo[b]tiophen-3-ol derivatives as effective inhibitors of human monoamine oxidase: design, synthesis, and biological activity

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.1511-1525

2019

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Inhibition of lysine acetyltransferases impairs tumor angiogenesis acting on both endothelial and tumor cells

Journal of experimental & clinical cancer research, 2020-06, Vol.39 (1), p.103-103, Article 103

2020

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A Novel Histone Acetyltransferase Inhibitor Modulating Gcn5 Network: Cyclopentylidene-[4-(4′-chlorophenyl)thiazol-2-yl)hydrazone

Journal of medicinal chemistry, 2009-01, Vol.52 (2), p.530-536

2009

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Synthesis and evaluation of a large library of nitroxoline derivatives as pancreatic cancer antiproliferative agents

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.1331-1344

2020

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Synthesis and biological evaluation of anti-Toxoplasma gondii activity of a novel scaffold of thiazolidinone derivatives

Journal of enzyme inhibition and medicinal chemistry, 2017-01, Vol.32 (1), p.746-758

2017

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Kinetic Study on the Base-Catalyzed Imine-Enamine Tautomerism of a Chiral Biologically Active Isoxazoline Derivative by HPLC on Amylose Tris(3,5-dimethylphenylcarbamate) Chiral Stationary Phase

Selective MAO-B inhibitors: a lesson from natural products

Chiral Hydroxy Metabolite of Mebendazole: Analytical and Semi-Preparative High-Performance Liquid Chromatography Resolution and Chiroptical Properties

Novel Insights on Human Carbonic Anhydrase Inhibitors Based on Coumalic Acid: Design, Synthesis, Molecular Modeling Investigation, and Biological Studies

Synthesis and Evaluation of Thymol-Based Synthetic Derivatives as Dual-Action Inhibitors against Different Strains of H. pylori and AGS Cell Line

4-(3-Nitrophenyl)thiazol-2-ylhydrazone derivatives as antioxidants and selective hMAO-B inhibitors: synthesis, biological activity and computational analysis

Open saccharin-based secondary sulfonamides as potent and selective inhibitors of cancer-related carbonic anhydrase IX and XII isoforms

Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives

Design, Synthesis, Docking Studies and Monoamine Oxidase Inhibition of a Small Library of 1-acetyl- and 1-thiocarbamoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazoles

Synthesis, Molecular Modeling, and Selective Inhibitory Activity against Human Monoamine Oxidases of 3-Carboxamido-7-Substituted Coumarins

2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms

Synthesis, selective anti-Helicobacter pylori activity, and cytotoxicity of novel N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides

Neem oil nanoemulsions: characterisation and antioxidant activity

Meet Our Editorial Board Member

Exploring New Scaffolds for the Dual Inhibition of HIV-1 RT Polymerase and Ribonuclease Associated Functions

Synthesis and Biological Evaluation of Carvacrol-Based Derivatives as Dual Inhibitors of H. pylori Strains and AGS Cell Proliferation

Discovery and optimization of pyrazoline derivatives as promising monoamine oxidase inhibitors

Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold

Novel insights on saccharin- and acesulfame-based carbonic anhydrase inhibitors: design, synthesis, modelling investigations and biological activity evaluation

Atriplex mollis Desf. Aerial Parts: Extraction Procedures, Secondary Metabolites and Color Analysis

Benzo[b]tiophen-3-ol derivatives as effective inhibitors of human monoamine oxidase: design, synthesis, and biological activity

Inhibition of lysine acetyltransferases impairs tumor angiogenesis acting on both endothelial and tumor cells

A Novel Histone Acetyltransferase Inhibitor Modulating Gcn5 Network: Cyclopentylidene-[4-(4′-chlorophenyl)thiazol-2-yl)hydrazone

Synthesis and evaluation of a large library of nitroxoline derivatives as pancreatic cancer antiproliferative agents

Synthesis and biological evaluation of anti-Toxoplasma gondii activity of a novel scaffold of thiazolidinone derivatives

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