Publications by authors named "Claudia Piutti"

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ADME properties of CHF6366, a novel bi-functional M3 muscarinic receptor antagonist and ß adrenoceptor agonist (MABA) radiolabelled at both functional moieties.
Alberto Ghiglieri, Monica Messina, Valentina Cenacchi, Claudia Piutti, Flavio Cinato

Xenobiotica· April 2023

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Stereoselective synthesis of 3,4-dihydropyrrolo[1,2-a]pyrazin-1(2H)-one derivatives as PIM kinase inhibitors inspired from marine alkaloids.
Francesco Casuscelli, Elena Ardini, Nilla Avanzi, Alessandra Badari, Elena Casale, Claudia Piutti

Chirality· November 2022

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Plasma-enhanced protein patterning in a microfluidic compartmentalized platform for multi-organs-on-chip: a liver-tumor model.
Erika Ferrari, Giovanni Stefano Ugolini, Claudia Piutti, Simona Marzorati, Marco Rasponi

Biomed Mater· June 2021

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Discovery and optimization of pyrrolo[1,2-a]pyrazinones leads to novel and selective inhibitors of PIM kinases.
Francesco Casuscelli, Elena Ardini, Nilla Avanzi, Elena Casale, Giovanni Cervi, Claudia Piutti

Bioorg Med Chem· December 2013

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The Piancatelli rearrangement: new applications for an intriguing reaction.
Claudia Piutti, Francesca Quartieri

Molecules· October 2013

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A submarine journey: the pyrrole-imidazole alkaloids.
Barbara Forte, Beatrice Malgesini, Claudia Piutti, Francesca Quartieri, Alessandra Scolaro

Mar Drugs· November 2009

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3-Aminopyrazole inhibitors of CDK2/cyclin A as antitumor agents. 2. Lead optimization.
Paolo Pevarello, Maria Gabriella Brasca, Paolo Orsini, Gabriella Traquandi, Antonio Longo, Claudia Piutti

J Med Chem· April 2005

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3-Aminopyrazole inhibitors of CDK2/cyclin A as antitumor agents. 1. Lead finding.
Paolo Pevarello, Maria Gabriella Brasca, Raffaella Amici, Paolo Orsini, Gabriella Traquandi, Claudia Piutti

J Med Chem· June 2004

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Total synthesis of the amaryllidaceae alkaloid (+)-plicamine and its unnatural enantiomer by using solid-supported reagents and scavengers in a multistep sequence of reactions.
Ian R Baxendale, Steven V Ley, Claudia Piutti

Angew Chem Int Ed Engl· June 2002

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