| Literature DB >> 30996808 |
Leda Ivanova Bencheva1, Marilenia De Matteo1, Luca Ferrante1, Marco Ferrara1, Adolfo Prandi1, Pietro Randazzo1, Silvano Ronzoni1, Roberta Sinisi1, Pierfausto Seneci1,2, Vincenzo Summa3, Mariana Gallo3, Maria Veneziano3, Antonella Cellucci3, Nausicaa Mazzocchi4, Andrea Menegon4, Romano Di Fabio1,3.
Abstract
Acid-sensing ion channels (ASICs) are a family of ion channels permeable to cations and largely responsible for the onset of acid-evoked ion currents both in neurons and in different types of cancer cells, thus representing a potential target for drug discovery. Owing to the limited attention ASIC2 has received so far, an exploratory program was initiated to identify ASIC2 inhibitors using diminazene, a known pan-ASIC inhibitor, as a chemical starting point for structural elaboration. The performed exploration enabled the identification of a novel series of ASIC2 inhibitors. In particular, compound 2u is a brain penetrant ASIC2 inhibitor endowed with an optimal pharmacokinetic profile. This compound may represent a useful tool to validate in animal models in vivo the role of ASIC2 in different neurodegenerative central nervous system pathologies.Entities:
Year: 2019 PMID: 30996808 PMCID: PMC6466820 DOI: 10.1021/acsmedchemlett.8b00591
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345