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Journal of Medicinal Chemistry|April 28, 2016
H2S-Donating Doxorubicins May Overcome Cardiotoxicity and Multidrug ResistanceKonstantin Chegaev, Barbara Rolando, Daniela Cortese, et al.Molecular Pharmaceutics|July 3, 2019
Validation of Thiosemicarbazone Compounds as P-Glycoprotein Inhibitors in Human Primary Brain-Blood Barrier and Glioblastoma Stem CellsIris Chiara Salaroglio, Carmen Abate, Barbara Rolando, et al.Molecular Pharmaceutics|August 30, 2019
Paracetamol-Galactose Conjugate: A Novel Prodrug for an Old Analgesic DrugFederica Sodano, Loretta Lazzarato, Barbara Rolando, et al.Chemmedchem|August 7, 2012
Designing multitarget anti-inflammatory agents: chemical modulation of the lumiracoxib structure toward dual thromboxane antagonists-COX-2 inhibitorsMassimo Bertinaria, Mohammed Abrar Abdul Gaffar Shaikh, Carola Buccellati, et al.Medchemcomm|August 16, 2018
New tetrahydroisoquinoline-based P-glycoprotein modulators: decoration of the biphenyl core gives selective ligandsMarialessandra Contino, Stefano Guglielmo, Maria Grazia Perrone, et al.Pharmaceuticals (Basel, Switzerland)|November 27, 2021
Ketogal Safety Profile in Human Primary Colonic Epithelial Cells and in MiceFederica Sodano, Bice Avallone, Monica Tizzano, et al.Small Science|August 21, 2025
Hyaluronic Acid-Decorated Liposomes for the Intrapulmonary Delivery of Imatinib: A Targeted Treatment for Postinflammatory Pulmonary FibrosisSara Bozzini, Valeria Bincoletto, Laura Pandolfi, et al.Journal of Medicinal Chemistry|April 23, 2010
4-hydroxy-1,2,5-oxadiazol-3-yl moiety as bioisoster of the carboxy function. Synthesis, ionization constants, and molecular pharmacological characterization at ionotropic glutamate receptors of compounds related to glutamate and its homologuesMarco L Lolli, Cecilia Giordano, Darryl S Pickering, et al.European Journal of Medicinal Chemistry|April 21, 2022
New aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the hydroxytriazole scaffoldAgnese Chiara Pippione, Zühal Kilic-Kurt, Sandra Kovachka, et al.Molecules (Basel, Switzerland)|December 11, 2022
Investigation into the Use of Encorafenib to Develop Potential PROTACs Directed against BRAFV600E ProteinElisabetta Marini, Marco Marino, Giulia Gionfriddo, et al.Pageof 11