calcoloscientifico:risulati
Differenze
Queste sono le differenze tra la revisione selezionata e la versione attuale della pagina.
| Entrambe le parti precedenti la revisione Revisione precedente | Ultima revisione Entrambe le parti successive la revisione | ||
|
calcoloscientifico:risulati [16/02/2024 10:22] fausto.pagani |
calcoloscientifico:risulati [16/02/2024 10:23] fausto.pagani |
||
|---|---|---|---|
| Linea 37: | Linea 37: | ||
| === 2022 === | === 2022 === | ||
| + | * Elisi GM, Scalvini L, Lodola A, Mor M, Rivara S. Free-energy simulations support a lipophilic binding route for melatonin receptors. J. Chem. Inf. Model. 2022 62, 210-222. | ||
| * Galvani F, Scalvini L, Rivara S, Lodola A, Mor M. Mechanistic modeling of monoglyceride lipase covalent modification elucidates the role of leaving group expulsion and discriminates inhibitors with high and low potency. J. Chem. Inf. Model. 2022 62, 2771-2787. | * Galvani F, Scalvini L, Rivara S, Lodola A, Mor M. Mechanistic modeling of monoglyceride lipase covalent modification elucidates the role of leaving group expulsion and discriminates inhibitors with high and low potency. J. Chem. Inf. Model. 2022 62, 2771-2787. | ||
| * Mari M, Elisi GM, Bedini A, Lucarini S, Retini M, Lucini V, Scaglione F, Vincenzi F, Varani K, Castelli R, Mor M, Rivara S, Spadoni G. 2-Arylmelatonin analogues: probing the 2-phenyl binding pocket of melatonin MT1 and MT2 receptors. Eur. J. Med. Chem. 2022 243:114762. | * Mari M, Elisi GM, Bedini A, Lucarini S, Retini M, Lucini V, Scaglione F, Vincenzi F, Varani K, Castelli R, Mor M, Rivara S, Spadoni G. 2-Arylmelatonin analogues: probing the 2-phenyl binding pocket of melatonin MT1 and MT2 receptors. Eur. J. Med. Chem. 2022 243:114762. | ||
calcoloscientifico/risulati.txt ยท Ultima modifica: 11/03/2024 10:10 da fausto.pagani
Strumenti Pagina
