Her primary scientific interests are in Acetylcholinesterase, Enzyme inhibitor, Biochemistry, Structure–activity relationship and Stereochemistry. Her Acetylcholinesterase research integrates issues from In vitro, Binding site and Amyloid precursor protein. Manuela Bartolini has researched Enzyme inhibitor in several fields, including Mechanism of action and Circular dichroism.
Her work in Biochemistry addresses subjects such as Alzheimer's disease, which are connected to disciplines such as Neurodegeneration and Neuroscience. Within one scientific family, Manuela Bartolini focuses on topics pertaining to Lead compound under Structure–activity relationship, and may sometimes address concerns connected to Anti alzheimer, Reactive oxygen species, Lipoic acid and Pharmacophore. In general Stereochemistry, her work in Quantitative structure–activity relationship is often linked to Structure based linking many areas of study.
Manuela Bartolini mainly investigates Acetylcholinesterase, Pharmacology, Stereochemistry, Biochemistry and Tacrine. Her Acetylcholinesterase research is multidisciplinary, incorporating elements of Structure–activity relationship, Enzyme inhibitor and Cholinesterase. Her Pharmacology course of study focuses on Disease and Drug discovery and Neuroscience.
Manuela Bartolini combines subjects such as Lead compound, Binding site and Active site with her study of Stereochemistry. Her Amyloid research extends to Biochemistry, which is thematically connected. The Tacrine study combines topics in areas such as Pharmacophore and IC50.
Her scientific interests lie mostly in Pharmacology, Acetylcholinesterase, Tacrine, Butyrylcholinesterase and In vitro. Her work deals with themes such as Disease, Catalase and Ligand, which intersect with Pharmacology. Her Acetylcholinesterase research incorporates elements of Neurotoxicity and Toxicity.
Her study in Tacrine is interdisciplinary in nature, drawing from both Cholinergic, Agonist, IC50, Pharmacophore and Structure–activity relationship. Her Butyrylcholinesterase study incorporates themes from Oxidative stress and Potency. The various areas that Manuela Bartolini examines in her In vitro study include Anti alzheimer, Human serum albumin, Circular dichroism and Amyloid.
Manuela Bartolini focuses on Tacrine, Pharmacology, Acetylcholinesterase, Butyrylcholinesterase and Neuroprotection. Her Tacrine study is related to the wider topic of Enzyme. Her research in Pharmacology focuses on subjects like Ligand, which are connected to Cholinesterase.
Her Acetylcholinesterase study combines topics in areas such as Pharmacophore and Structure–activity relationship. Manuela Bartolini has included themes like Stereochemistry, GSK-3, Cell growth and Cytotoxicity in her Structure–activity relationship study. Her Neuroprotection research includes elements of Alzheimer's disease and Cannabinoid receptor, Cannabinoid receptor type 2.
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β-Amyloid aggregation induced by human acetylcholinesterase: inhibition studies
Manuela Bartolini;Carlo Bertucci;Vanni Cavrini;Vincenza Andrisano.
Biochemical Pharmacology (2003)
Insight Into the Kinetic of Amyloid β (1–42) Peptide Self‐Aggregation: Elucidation of Inhibitors’ Mechanism of Action
Manuela Bartolini;Carlo Bertucci;Maria Laura Bolognesi;Andrea Cavalli.
ChemBioChem (2007)
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)
Rational approach to discover multipotent anti-Alzheimer drugs.
Michela Rosini;Vincenza Andrisano;Manuela Bartolini;Maria L. Bolognesi.
Journal of Medicinal Chemistry (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)
Design, synthesis, and biological evaluation of dual binding site acetylcholinesterase inhibitors: new disease-modifying agents for Alzheimer's disease.
Pilar Munoz-Ruiz;Laura Rubio;Esther Garcia-Palomero;Isabel Dorronsoro.
Journal of Medicinal Chemistry (2005)
Inhibition of Acetylcholinesterase, β-Amyloid Aggregation, and NMDA Receptors in Alzheimer’s Disease: A Promising Direction for the Multi-target-Directed Ligands Gold Rush
Michela Rosini;Elena Simoni;Manuela Bartolini;Andrea Cavalli.
Journal of Medicinal Chemistry (2008)
Pyrano[3,2-c]quinoline−6-Chlorotacrine Hybrids as a Novel Family of Acetylcholinesterase- and β-Amyloid-Directed Anti-Alzheimer Compounds
Pelayo Camps;Xavier Formosa;Carles Galdeano;Diego Muñoz-Torrero.
Journal of Medicinal Chemistry (2009)
A small molecule targeting the multifactorial nature of Alzheimer's disease.
Andrea Cavalli;Maria Laura Bolognesi;Simona Capsoni;Vincenza Andrisano.
Angewandte Chemie (2007)
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