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Journal of Medicinal Chemistry|May 24, 2019
Five-Membered N-Heterocyclic Scaffolds as Novel Amino Bioisosteres at γ-Aminobutyric Acid (GABA) Type A Receptors and GABA TransportersAlessandro Giraudo, Jacob Krall, Francesco Bavo, et al.International Journal of Molecular Sciences|December 30, 2020
Extracellular Matrix Composition Modulates the Responsiveness of Differentiated and Stem Pancreatic Cancer Cells to Lipophilic Derivate of GemcitabineStefania Forciniti, Elisa Dalla Pozza, Maria Raffaella Greco, et al.European Journal of Pharmaceutics and Biopharmaceutics : Official Journal of Arbeitsgemeinschaft Fur Pharmazeutische Verfahrenstechnik E.V|August 4, 2025
A new biocompatible butyric acid-releasing glucosamine derivative for transdermal deliveryMarica Erminia Schiano, Ritamaria Di Lorenzo, Teresa Di Serio, et al.Pharmaceutics|January 30, 2020
Curcumin-Loaded Solid Lipid Nanoparticles Bypass P-Glycoprotein Mediated Doxorubicin Resistance in Triple Negative Breast Cancer CellsGamal-Eldein Fathy Abd-Ellatef, Elena Gazzano, Daniela Chirio, et al.Scientific Reports|April 9, 2024
Identification of small molecules affecting the interaction between human hemoglobin and Staphylococcus aureus IsdB hemophoreMonica Cozzi, Mariacristina Failla, Eleonora Gianquinto, et al.European Journal of Medicinal Chemistry|March 19, 2026
Structure-based design of new pyrazole inhibitors targeting Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH)Agnese C Pippione, Noemi Villella, Federico Fornaseri, et al.European Journal of Medicinal Chemistry|December 12, 2018
Hydroxyazole scaffold-based Plasmodium falciparum dihydroorotate dehydrogenase inhibitors: Synthesis, biological evaluation and X-ray structural studiesAgnese C Pippione, Stefano Sainas, Parveen Goyal, et al.Journal of Medicinal Chemistry|June 26, 2018
Targeting Myeloid Differentiation Using Potent 2-Hydroxypyrazolo[1,5- a]pyridine Scaffold-Based Human Dihydroorotate Dehydrogenase InhibitorsStefano Sainas, Agnese C Pippione, Elisa Lupino, et al.Journal of Medicinal Chemistry|October 22, 2025
Exploiting the 2-(1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)acetic Acid Scaffold to Generate COXTRANs: A New Class of Dual Cyclooxygenase Inhibitors-Thromboxane Receptor AntagonistsFederica Blua, Francesca Boccato, Carola Buccellati, et al.Journal of Advanced Research|January 13, 2022
H2S donating corticosteroids: Design, synthesis and biological evaluation in a murine model of asthmaAngela Corvino, Valentina Citi, Ferdinando Fiorino, et al.Pageof 11