As part of his studies on Lipophilicity, Maurizio Recanatini often connects relevant subjects like Organic chemistry. His study on Organic chemistry is mostly dedicated to connecting different topics, such as Lipophilicity. Reversed-phase chromatography and Phase (matter) are commonly linked in his work. His Phase (matter) study frequently draws connections between related disciplines such as Reversed-phase chromatography. His research on Stationary phase frequently connects to adjacent areas such as Chromatography. His research ties Stationary phase and Chromatography together. Maurizio Recanatini combines High-performance liquid chromatography and Hydrophilic interaction chromatography in his studies. By researching both Hydrophilic interaction chromatography and High-performance liquid chromatography, he produces research that crosses academic boundaries. He connects Thin-layer chromatography with High performance thin layer chromatography in his research.
Chromatography and Stationary phase are commonly linked in his work. Maurizio Recanatini connects Organic chemistry with Triazine in his study. By researching both Lipophilicity and Partition coefficient, Maurizio Recanatini produces research that crosses academic boundaries. Maurizio Recanatini undertakes interdisciplinary study in the fields of Partition coefficient and Lipophilicity through his research. His High-performance liquid chromatography study frequently intersects with other fields, such as Capacity factor. In most of his Capacity factor studies, his work intersects topics such as High-performance liquid chromatography. Maurizio Recanatini merges many fields, such as Enzyme and Acetylcholinesterase, in his writings. Maurizio Recanatini performs multidisciplinary study in the fields of Acetylcholinesterase and Enzyme via his papers. His research is interdisciplinary, bridging the disciplines of Glycoside and Stereochemistry.
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Multi-Target-Directed Ligands To Combat Neurodegenerative Diseases
Andrea Cavalli;Maria Laura Bolognesi;Anna Minarini;Michela Rosini.
Journal of Medicinal Chemistry (2008)
Toward a pharmacophore for drugs inducing the long QT syndrome: insights from a CoMFA study of HERG K(+) channel blockers.
Andrea Cavalli;Elisabetta Poluzzi;Fabrizio De Ponti;Maurizio Recanatini.
Journal of Medicinal Chemistry (2002)
Safety of non-antiarrhythmic drugs that prolong the QT interval or induce torsade de pointes: an overview.
Fabrizio De Ponti;Elisabetta Poluzzi;Andrea Cavalli;Maurizio Recanatini.
Drug Safety (2002)
3-(4-{[Benzyl(methyl)amino]methyl}phenyl)-6,7-dimethoxy-2H-2-chromenone (AP2238) Inhibits Both Acetylcholinesterase and Acetylcholinesterase-Induced β-Amyloid Aggregation: A Dual Function Lead for Alzheimer's Disease Therapy§
Lorna Piazzi;Angela Rampa;Alessandra Bisi;Silvia Gobbi.
Journal of Medicinal Chemistry (2003)
Multi-target-directed drug design strategy: from a dual binding site acetylcholinesterase inhibitor to a trifunctional compound against Alzheimer's disease.
Maria Laura Bolognesi;Andrea Cavalli;Luca Valgimigli;Manuela Bartolini.
Journal of Medicinal Chemistry (2007)
QT prolongation through hERG K(+) channel blockade: current knowledge and strategies for the early prediction during drug development.
Maurizio Recanatini;Elisabetta Poluzzi;Matteo Masetti;Andrea Cavalli.
Medicinal Research Reviews (2005)
Multi-target-directed coumarin derivatives: hAChE and BACE1 inhibitors as potential anti-Alzheimer compounds.
Lorna Piazzi;Andrea Cavalli;Francesco Colizzi;Federica Belluti.
Bioorganic & Medicinal Chemistry Letters (2008)
A small molecule targeting the multifactorial nature of Alzheimer's disease.
Andrea Cavalli;Maria Laura Bolognesi;Simona Capsoni;Vincenza Andrisano.
Angewandte Chemie (2007)
SAR of 9-Amino-1,2,3,4-tetrahydroacridine-Based Acetylcholinesterase Inhibitors: Synthesis, Enzyme Inhibitory Activity, QSAR, and Structure-Based CoMFA of Tacrine Analogues
Maurizio Recanatini;Andrea Cavalli;Federica Belluti;Lorna Piazzi.
Journal of Medicinal Chemistry (2000)
Single-molecule pulling simulations can discern active from inactive enzyme inhibitors.
Francesco Colizzi;Remo Perozzo;Leonardo Scapozza;Maurizio Recanatini.
Journal of the American Chemical Society (2010)
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