Angela Stefanachi

Papers authored by Angela Stefanachi

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2012 Stolfa Da, Diana A. Stolfa, Angela Stefanachi

, Julia M. Gajer, Gajer Jm, Angela Nebbioso, Lucia Altucci, Saverio Cellamare, Manfred Jung

, Angelo Carotti

Design, synthesis and biological evaluation of 2-aminobenzanilide derivatives as potent and selective HDAC inhibitors

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2011 Raffaella Zoe Pellicani, Pellicani Rz, Angela Stefanachi

, Mauro Niso, Angelo Carotti, Francesco Leonetti, Orazio Nicolotti

, Roberto Perrone, Francesco Berardi, Saverio Cellamare, Nicola Antonio Colabufo, Colabufo Na

Potent Galloyl-Based Selective Modulators Targeting Multidrug Resistance Associated Protein 1 and P-glycoprotein

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Ilenia Giangreco, Gianluca Lattanzi, Orazio Nicolotti

, Marco Catto

, Antonio Laghezza, Francesco Leonetti, Angela Stefanachi

, Angelo Carotti

Insights into the Complex Formed by Matrix Metalloproteinase-2 and Alloxan Inhibitors: Molecular Dynamics Simulations and Free Energy Calculations

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L. Pisani, M. Catto

, F. Leonetti, O. Nicolotti

, A. Stefanachi

, F. Campagna, A. Carotti,

Targeting Monoamine Oxidases with Multipotent Ligands: An Emerging Strategy in the Search of New Drugs Against Neurodegenerative Diseases

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F. Leonetti, A. Stefanachi

, O. Nicolotti

, M. Catto

, L. Pisani, S. Cellamare, A. Carotti,

BCR-ABL Inhibitors in Chronic Myeloid Leukemia: Process Chemistry and Biochemical Profile

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Orazio Nicolotti

, Ilenia Giangreco, Antonellina Introcaso, Francesco Leonetti, Angela Stefanachi

, Angelo Carotti

Strategies of multi-objective optimization in drug discovery and development

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Orazio Nicolotti

, Leonardo Pisani, Marco Catto

, Francesco Leonetti, Ilenia Giangreco, Angela Stefanachi

, Angelo Carotti

Discovery of a Potent and Selective Hetero-Bivalent AChE Inhibitor via Bioisosteric Replacement

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Angela Stefanachi

, Angelo D. Favia, Orazio Nicolotti

, Francesco Leonetti, Leonardo Pisani, Marco Catto

, Christina Zimmer, Rolf W. Hartmann, Angelo Carotti

Design, Synthesis, and Biological Evaluation of Imidazolyl Derivatives of 4,7-Disubstituted Coumarins as Aromatase Inhibitors Selective over 17-α-Hydroxylase/C17−20 Lyase

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2010 Leonardo Pisani, Marco Catto

, Ilenia Giangreco, Francesco Leonetti, Orazio Nicolotti

, Angela Stefanachi

, Saverio Cellamare, Angelo Carotti

Design, Synthesis, and Biological Evaluation of Coumarin Derivatives Tethered to an Edrophonium‐like Fragment as Highly Potent and Selective Dual Binding Site Acetylcholinesterase Inhibitors

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Giovanni Pellegrino, Francesco Leonetti, Angelo Carotti, Orazio Nicolotti

, Leonardo Pisani, Angela Stefanachi

, Marco Catto

Solid phase synthesis of a molecular library of pyrimidines, pyrazoles, and isoxazoles with biological potential

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2009 Franco Fernández, Olga Caamaño, M. Isabel Nieto, Nieto Mi, Carmen López, Xerardo García-Mera, Angela Stefanachi

, Orazio Nicolotti

, M. Isabel Loza, Loza Mi, Jose Brea, Cristina Esteve, Victor Segarra, Bernat Vidal, Angelo Carotti

1,3-Dialkyl-8-N-substituted benzyloxycarbonylamino-9-deazaxanthines as potent adenosine receptor ligands: Design, synthesis, structure–affinity and structure–selectivity relationships

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2008 Alberto Coelho

, Abel Crespo, Franco Fernandez, PierFrancesco F. Biagini, Angela Stefanachi

, Eddy Sotelo, E.

Synthetic Applications of Polystyrene-Supported 1,1,3,3-Tetramethylguanidine

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Angela Stefanachi

, Orazio Nicolotti

, Francesco Leonetti, Saverio Cellamare, Francesco Campagna, Maria Isabel Loza

, Loza Mi, Jose Manuel Brea, Brea Jm, Fernando Mazza, Enrico Gavuzzo, Angelo Carotti

1,3-Dialkyl-8-(hetero)aryl-9-OH-9-deazaxanthines as potent A2B adenosine receptor antagonists: Design, synthesis, structure–affinity and structure–selectivity relationships

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Francesco Leonetti, Marco Catto

, Orazio Nicolotti

, Leonardo Pisani, Anna Cappa, Angela Stefanachi

, Angelo Carotti

Homo- and hetero-bivalent edrophonium-like ammonium salts as highly potent, dual binding site AChE inhibitors

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Saverio Cellamare, Angela Stefanachi

, Diana A. Stolfa, Teodora Basile, Marco Catto

, Francesco Campagna, Eddy Sotelo, Pasquale Acquafredda, Angelo Carotti

Design, synthesis, and biological evaluation of glycine-based molecular tongs as inhibitors of Aβ1-40 aggregation in vitro

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Angela Stefanachi

, B. Vidal, Jose Manuel Brea, Maria Isabel Cadavid, Nuria B. Centeno, Cristina Esteve, Maria Isabel Loza

, Ana Martinez, Rosa Nieto, V. Segarra, Enrique Raviña, Ferran Sanz, E. Sotelo, A. Carotti

1-, 3- and 8-substituted-9-deazaxanthines as potent and selective antagonists at the human A2B adenosine receptor

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

A. Stefanachi

, J. M. Brea, M. I. Cadavid, N. B. Centeno, C. Esteve, M. I. Loza, A. Martinez, R. Nieto, E. Raviña, F. Sanz, Segarra, E. Sotelo, B. Vidal, A. Carotti

Corrigendum to "1-, 3- and 8-substituted-9-deazaxanthines as potent and selective antagonists at the human A2B adenosine receptor" [Bioorg. Med. Chem. 16 (2008) 2852-2869] (DOI:10.1016/j.bmc.2008.01.002)

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2007 Francesco Leonetti, Carmelida Capaldi, Leonardo Pisani, Orazio Nicolotti

, Giovanni Muncipinto, Angela Stefanachi

, Saverio Cellamare, Carla Caccia, Angelo Carotti

Solid-Phase Synthesis and Insights into Structure−Activity Relationships of Safinamide Analogues as Potent and Selective Inhibitors of Type B Monoamine Oxidase

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2005 Angelo Carotti, Maria Isabel Cadavid, Cadavid Mi, Nuria B. Centeno, Centeno Nb, Cristina Esteve, Maria Isabel Loza

, Loza Mi, Ana Martinez, Rosa Nieto, Enrique Raviña, Ferran Sanz, Victor Segarra, Eddy Sotelo, Angela Stefanachi

and 1 other authors

Design, synthesis, and structure-activity relationships of 1-,3-,8-, and 9-substituted-9-deazaxanthines at the human A2B adenosine receptor

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2004 A. Carotti, A. Stefanachi

, E. Raviña, E. Sotelo, M. I. Loza, M. I. Cadavid, N. B. Centeno, O. Nicolotti

8-Substituted-9-deazaxanthines as adenosine receptor ligands: Design, synthesis and structure-affinity relationships at A 2B

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Papers authored by Angela Stefanachi