1023694-79-2Relevant academic research and scientific papers
Novel uracil-based 2-aminoanilide and 2-aminoanilide-like derivatives: Histone deacetylase inhibition and in-cell activities
Mai, Antonello,Perrone, Andrea,Nebbioso, Angela,Rotili, Dante,Valente, Sergio,Tardugno, Maria,Massa, Silvio,De Bellis, Floriana,Altucci, Lucia
, p. 2530 - 2535 (2008/12/21)
A novel series of non-hydroxamate HDAC inhibitors (HDACi) showing a uracil group at the left and a 2-aminoanilide/2-aminoanilide-like portion at the right head have been reported. In particular, the new compounds incorporating a 2-aminoanilide moiety behaved as class I-selective HDACi. Compound 8, the most potent and class I-selective, showed weak apoptosis (higher than MS-275) joined to cytodifferentiating activity on U937 cells. Surprisingly, the highest differentiation was observed with 13, through an effect that seems to be unrelated to HDAC inhibition.
