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Giulio Rastelli

Showing results (81-90 of 93) with videos related to

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European Journal of Medicinal Chemistry|July 30, 2025
Design, synthesis, and biological evaluation of chalcone derivatives as selective Monoamine Oxidase-B inhibitors with potential neuroprotective effectsGiorgio Facchetti, Sara Marchese, Valentina Coccè, et al.
The Journal of Biological Chemistry|August 17, 2002
Oxidative modification of aldose reductase induced by copper ion. Definition of the metal-protein interaction mechanismIlaria Cecconi, Andrea Scaloni, Giulio Rastelli, et al.
ACS Medicinal Chemistry Letters|July 15, 2021
Promising Non-cytotoxic Monosubstituted Chalcones to Target Monoamine Oxidase-BLuca G Iacovino, Luca Pinzi, Giorgio Facchetti, et al.
Chemmedchem|November 19, 2016
Probing an Allosteric Pocket of CDK2 with Small MoleculesMichael S Christodoulou, Fabiana Caporuscio, Valentina Restelli, et al.
Scientific Reports|December 11, 2025
Design, synthesis and biological activity of glycoconjugated ADAMTS5 exosite inhibitors: applications in osteoarthritis and ovarian cancer modelsDoretta Cuffaro, Sophie Blagg, Kazuhiro Yamamoto, et al.
Journal of Medicinal Chemistry|January 10, 2019
Evaluation of Amides, Carbamates, Sulfonamides, and Ureas of 4-Prop-2-ynylidenecycloalkylamine as Potent, Selective, and Bioavailable Negative Allosteric Modulators of Metabotropic Glutamate Receptor 5Davide Graziani, Silvia Caligari, Elisa Callegari, et al.
Journal of Medicinal Chemistry|June 4, 2015
Discovery of Multitarget Antivirals Acting on Both the Dengue Virus NS5-NS3 Interaction and the Host Src/Fyn KinasesPaolo Vincetti, Fabiana Caporuscio, Suzanne Kaptein, et al.
Chemmedchem|November 21, 2018
Structure-Activity Relationships of Hexahydrocyclopenta[c]quinoline Derivatives as Allosteric Inhibitors of CDK2 and EGFRLuca Carlino, Michael S Christodoulou, Valentina Restelli, et al.
European Journal of Medicinal Chemistry|December 14, 2022
Design, synthesis, biological evaluation and crystal structure determination of dual modulators of carbonic anhydrases and estrogen receptorsAnnachiara Tinivella, Jerome C Nwachukwu, Andrea Angeli, et al.
Nature Communications|February 23, 2024
Quantitative live cell imaging of a tauopathy model enables the identification of a polypharmacological drug candidate that restores physiological microtubule interactionLuca Pinzi, Christian Conze, Nicolo Bisi, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
European Journal of Medicinal Chemistry|July 30, 2025
Design, synthesis, and biological evaluation of chalcone derivatives as selective Monoamine Oxidase-B inhibitors with potential neuroprotective effectsGiorgio Facchetti, Sara Marchese, Valentina Coccè, et al.
The Journal of Biological Chemistry|August 17, 2002
Oxidative modification of aldose reductase induced by copper ion. Definition of the metal-protein interaction mechanismIlaria Cecconi, Andrea Scaloni, Giulio Rastelli, et al.
ACS Medicinal Chemistry Letters|July 15, 2021
Promising Non-cytotoxic Monosubstituted Chalcones to Target Monoamine Oxidase-BLuca G Iacovino, Luca Pinzi, Giorgio Facchetti, et al.
Chemmedchem|November 19, 2016
Probing an Allosteric Pocket of CDK2 with Small MoleculesMichael S Christodoulou, Fabiana Caporuscio, Valentina Restelli, et al.
Scientific Reports|December 11, 2025
Design, synthesis and biological activity of glycoconjugated ADAMTS5 exosite inhibitors: applications in osteoarthritis and ovarian cancer modelsDoretta Cuffaro, Sophie Blagg, Kazuhiro Yamamoto, et al.
Journal of Medicinal Chemistry|January 10, 2019
Evaluation of Amides, Carbamates, Sulfonamides, and Ureas of 4-Prop-2-ynylidenecycloalkylamine as Potent, Selective, and Bioavailable Negative Allosteric Modulators of Metabotropic Glutamate Receptor 5Davide Graziani, Silvia Caligari, Elisa Callegari, et al.
Journal of Medicinal Chemistry|June 4, 2015
Discovery of Multitarget Antivirals Acting on Both the Dengue Virus NS5-NS3 Interaction and the Host Src/Fyn KinasesPaolo Vincetti, Fabiana Caporuscio, Suzanne Kaptein, et al.
Chemmedchem|November 21, 2018
Structure-Activity Relationships of Hexahydrocyclopenta[c]quinoline Derivatives as Allosteric Inhibitors of CDK2 and EGFRLuca Carlino, Michael S Christodoulou, Valentina Restelli, et al.
European Journal of Medicinal Chemistry|December 14, 2022
Design, synthesis, biological evaluation and crystal structure determination of dual modulators of carbonic anhydrases and estrogen receptorsAnnachiara Tinivella, Jerome C Nwachukwu, Andrea Angeli, et al.
Nature Communications|February 23, 2024
Quantitative live cell imaging of a tauopathy model enables the identification of a polypharmacological drug candidate that restores physiological microtubule interactionLuca Pinzi, Christian Conze, Nicolo Bisi, et al.
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