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Monica Esposito

Research Profile

Chemicals & Drugs

Genes & Molecular Sequences

Amino Acid Sequences

Concepts & Ideas

Phenomena

Procedures

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Publications

TOP 3
Antonello Mai; Marino Artico; Monica Esposito; Rino Ragno; Gianluca Sbardella; Silvio Massa
Synthesis and biological evaluation of enantiomerically pure pyrrolyl-oxazolidinones as a new class of potent and selective monoamine oxidase type A inhibitors.
Antonello Mai; Silvio Massa; Rino Ragno; Monica Esposito; Gianluca Sbardella; Giuseppina Nocca; Roberto Scatena; Florian Jesacher; Peter Loidl; Gerald Brosch
Binding mode analysis of 3-(4-benzoyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiation.
Antonello Mai; Marino Artico; Monica Esposito; Gianluca Sbardella; Silvio Massa; Olivia Befani; Paola Turini; Valentina Giovannini; Bruno Mondovì
3-(1H-Pyrrol-1-yl)-2-oxazolidinones as reversible, highly potent, and selective inhibitors of monoamine oxidase type A.

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All Publications

2003: Antonello Mai; Marino Artico; Monica Esposito; Rino Ragno; Gianluca Sbardella; Silvio Massa
Synthesis and biological evaluation of enantiomerically pure pyrrolyl-oxazolidinones as a new class of potent and selective monoamine oxidase type A inhibitors.
Farmaco (Società chimica italiana : 1989) 2003;58(3):231-41.
2002: Antonello Mai; Silvio Massa; Rino Ragno; Monica Esposito; Gianluca Sbardella; Giuseppina Nocca; Roberto Scatena; Florian Jesacher; Peter Loidl; Gerald Brosch
Binding mode analysis of 3-(4-benzoyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiation.
Journal of medicinal chemistry 2002;45(9):1778-84.
2002: Antonello Mai; Marino Artico; Monica Esposito; Gianluca Sbardella; Silvio Massa; Olivia Befani; Paola Turini; Valentina Giovannini; Bruno Mondovì
3-(1H-Pyrrol-1-yl)-2-oxazolidinones as reversible, highly potent, and selective inhibitors of monoamine oxidase type A.
Journal of medicinal chemistry 2002;45(6):1180-3.

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