J. Med. Chem., 2013, 56 (17), pp 6666–6680
New Anticancer Agents Mimicking Protein Recognition Motifs
Marco Persico †, Anna Ramunno *‡, Vita Maglio ‡, Silvia Franceschelli *‡, Chiara Esposito ‡, Alfonso Carotenuto †, Diego Brancaccio †, Valeria De Pasquale §, Luigi Michele Pavone §, Michela Varra †, Nausicaa Orteca †, Ettore Novellino †, and Caterina Fattorusso *†
† Dipartimento di Farmacia, Università di Napoli “Federico II”, Via D. Montesano 49, 80131 Napoli, Italy
‡ Dipartimento di Farmacia, Università di Salerno, Via Giovanni Paolo II 132, 84084 Fisciano (SA), Italy
§ Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli “Federico II”, Via S. Pansini 5, 80131 Napoli, Italy
DOI: 10.1021/jm400947b
Abstract
The novel tetrasubstituted pyrrole derivatives 8g, 8h, and 8i showed selective cytotoxicity against M14 melanoma cells at low micromolar concentration. Structure–activity relationships (SARs) indicated the presence of three aromatic substituents on the pyrrole core as necessary for biological activity. Computational studies strongly suggest that the peculiar 3D orientation of these
substituents is able to reproduce the hydrophobic side chains in LxxLL-like protein recognition motifs. Biological results showed altered p53 expression and nuclear translocation in cells sensitive to the compounds, suggesting p53 involvement in their anticancer mechanism of action.
Unfortunately, because of poor solubility of the active analogues, it was not possible to perform further investigation by NMR techniques. Pharmacophore models were generated and used to perform 3D searches in molecular databases. Results indicated that two compounds share the same pharmacological profile and the same pharmacophoric features with our new derivatives, and one of them inhibited MDM2–MDM4 heterodimer formation.
