Abstract The protein arginine deiminase 4 (PAD4) is a calcium-dependent enzyme, which catalyses the irreversible conversion of peptidyl-arginines into peptidyl-citrullines and plays an important role in several diseases such as in the rheumatoid arthritis, multiple sclerosis, Alzheimer's disease, Creutzfeldt-Jacob's disease and cancer. In this study, we report the inhibition profiles and computational docking toward the PAD4 enzyme of a series of 1,2,3-triazole peptidomimetic-based derivatives incorporating the β-phenylalanine and guanidine scaffolds. Several effective, low micromolar PAD4 inhibitors are reported in this study.
Peptidomimetics as protein arginine deiminase 4 (PAD4) inhibitors / Trabocchi, Andrea; Pala, N.; Krimmelbein, I.; Menchi, Gloria; Guarna, Antonio; Sechi, M.; Dreker, T.; Scozzafava, Andrea; Supuran, CLAUDIU TRANDAFIR; Carta, Fabrizio. - In: JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY. - ISSN 1475-6366. - STAMPA. - 30:(2015), pp. 466-471. [10.3109/14756366.2014.947976]
Peptidomimetics as protein arginine deiminase 4 (PAD4) inhibitors.
TRABOCCHI, ANDREA;MENCHI, GLORIA;GUARNA, ANTONIO;SCOZZAFAVA, ANDREA;SUPURAN, CLAUDIU TRANDAFIR;CARTA, FABRIZIO
2015
Abstract
Abstract The protein arginine deiminase 4 (PAD4) is a calcium-dependent enzyme, which catalyses the irreversible conversion of peptidyl-arginines into peptidyl-citrullines and plays an important role in several diseases such as in the rheumatoid arthritis, multiple sclerosis, Alzheimer's disease, Creutzfeldt-Jacob's disease and cancer. In this study, we report the inhibition profiles and computational docking toward the PAD4 enzyme of a series of 1,2,3-triazole peptidomimetic-based derivatives incorporating the β-phenylalanine and guanidine scaffolds. Several effective, low micromolar PAD4 inhibitors are reported in this study.I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.