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.
2015
30
466
471
Trabocchi, Andrea; Pala, N.; Krimmelbein, I.; Menchi, Gloria; Guarna, Antonio; Sechi, M.; Dreker, T.; Scozzafava, Andrea; Supuran, CLAUDIU TRANDAFIR; Carta, Fabrizio
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/961062
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 18
  • ???jsp.display-item.citation.isi??? 15
social impact