Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
International Journal of Molecular Sciences|October 2, 2020
Cooperative Binding of the Cationic Porphyrin Tris-T4 Enhances Catalytic Activity of 20S Proteasome Unveiling a Complex Distribution of Functional StatesAnna Maria Santoro, Alessandro D'Urso, Alessandra Cunsolo, et al.
Journal of Medicinal Chemistry|May 16, 2008
Exploiting protein fluctuations at the active-site gorge of human cholinesterases: further optimization of the design strategy to develop extremely potent inhibitorsStefania Butini, Giuseppe Campiani, Marianna Borriello, et al.
Current Topics in Medicinal Chemistry|August 26, 2016
Benzodiazepine Scaffold as Drug-like Molecular Simplification of FR235222: A Chemical Tool for Exploring HDAC InhibitionRosario Randino, Ilaria Moronese, Elena Cini, et al.
International Journal of Molecular Sciences|February 20, 2020
Exploring the Photodynamic Properties of Two Antiproliferative Benzodiazopyrrole DerivativesConcetta Imperatore, Mohammadhassan Valadan, Luciana Tartaglione, et al.
Journal of Medicinal Chemistry|February 1, 2007
Design and synthesis of potent antimalarial agents based on clotrimazole scaffold: exploring an innovative pharmacophoreSandra Gemma, Giuseppe Campiani, Stefania Butini, et al.
Journal of Medicinal Chemistry|November 30, 2021
New Insights into the Structure-Activity Relationship and Neuroprotective Profile of Benzodiazepinone Derivatives of Neurounina-1 as Modulators of the Na+/Ca2+ Exchanger IsoformsElisa Magli, Caterina Fattorusso, Marco Persico, et al.
Chemmedchem|November 19, 2024
Eco-friendly Synthesis and Molecular Modelling of 2-Phenylimidazo[1,2-b]pyridazine Derivatives: In Vitro and In Vivo Studies for Lead OptimizationMarica Erminia Schiano, Chiara Billi, Giorgio Grillo, et al.
Journal of Medicinal Chemistry|March 18, 2005
Development of molecular probes for the identification of extra interaction sites in the mid-gorge and peripheral sites of butyrylcholinesterase (BuChE). Rational design of novel, selective, and highly potent BuChE inhibitorsGiuseppe Campiani, Caterina Fattorusso, Stefania Butini, et al.
European Journal of Medicinal Chemistry|May 13, 2021
Hybrids between H2S-donors and betamethasone 17-valerate or triamcinolone acetonide inhibit mast cell degranulation and promote hyperpolarization of bronchial smooth muscle cellsFlavia Giordano, Angela Corvino, Antonia Scognamiglio, et al.
Journal of Medicinal Chemistry|May 21, 2010
Discovery of bishomo(hetero)arylpiperazines as novel multifunctional ligands targeting dopamine D(3) and serotonin 5-HT(1A) and 5-HT(2A) receptorsStefania Butini, Giuseppe Campiani, Silvia Franceschini, et al.
Pageof 6