| Discovery of human hexosaminidase inhibitors by in situ screening of a library of mono-and divalent pyrrolidine iminosugars V Pingitore, M Martínez-Bailén, AT Carmona, Z Mészáros, N Kulik, ... Bioorganic Chemistry 120, 105650, 2022 | 14 | 2022 |
| Harnessing pyrrolidine iminosugars into dimeric structures for the rapid discovery of divalent glycosidase inhibitors AT Carmona, S Carrion-Jimenez, V Pingitore, E Moreno-Clavijo, I Robina, ... European Journal of Medicinal Chemistry 151, 765-776, 2018 | 13 | 2018 |
| Discovery of a potent α-galactosidase inhibitor by in situ analysis of a library of pyrrolizidine–(thio) urea hybrid molecules generated via click chemistry P Elías-Rodríguez, V Pingitore, AT Carmona, AJ Moreno-Vargas, D Ide, ... The Journal of Organic Chemistry 83 (16), 8863-8873, 2018 | 12 | 2018 |
| Development of the ULK1-Recruiting Chimeras (ULKRECs) to enable proximity-induced and ULK1-dependent degradation of mitochondria N Zaman, N Aley, V Pingitore, DL Selwood, R Ketteler bioRxiv, 2024.04. 15.589474, 2024 | 1 | 2024 |
| Reacciones Clic y evaluación in situ para la identificación de inhibidores de glicosidasas V Pingitore | 1 | 2021 |
| Delocalized quinolinium-macrocyclic peptides, an atypical chemotype for CNS penetration V Pingitore, J Pancholi, TW Hornsby, J Warne, G Pryce, LJ McCormick, ... Science Advances 10 (28), eado3501, 2024 | | 2024 |
