none7A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting two aromatic prion recognition motifs, was designed and evaluated against prion infection. Notably, 6-chloro-1,2,3,4-tetrahydroacridine 10 showed an EC(50) of 0.17 μM, which was lower than that displayed by reference compound BiCappa. More importantly, 10 possessed the capability to contrast prion fibril formation and oxidative stress, together with a low cytotoxicity. This study further corroborates the bivalent strategy as a viable approach to the rational design of anti-prion chemical probes.noneBongarzone S; Tran HN; Cavalli A; Roberti M; Carloni P; Legname G; Bolognesi ML.Bongarzone S; Tran HN; Cavalli A; Roberti M; Carloni P; Legn...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of th...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting two ...
A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting two ...
none5Prion diseases are prototypical conformational diseases. From a medicinal chemistry point of vi...
Prion diseases are characterized by the accumulation of a misfolded prion protein, PrPSc which deriv...
none5A small library combining two different benzoquinone cores with seven (L) amino acid methyl est...
Prion diseases are fatal neurodegenerative disorders that affect humans and animals and for which no...
Prion Diseases or Transmissible Spongiform Encephalopathies are neurodegenerative conditions associa...
2-Aminopyridine-3,5-dicarbonitrile compounds were previously identified as mimetics of dominant-nega...
Background: The main pathogenic event of prion disorders has been identified in the deposition of th...
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of th...
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of th...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of th...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting two ...
A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting two ...
none5Prion diseases are prototypical conformational diseases. From a medicinal chemistry point of vi...
Prion diseases are characterized by the accumulation of a misfolded prion protein, PrPSc which deriv...
none5A small library combining two different benzoquinone cores with seven (L) amino acid methyl est...
Prion diseases are fatal neurodegenerative disorders that affect humans and animals and for which no...
Prion Diseases or Transmissible Spongiform Encephalopathies are neurodegenerative conditions associa...
2-Aminopyridine-3,5-dicarbonitrile compounds were previously identified as mimetics of dominant-nega...
Background: The main pathogenic event of prion disorders has been identified in the deposition of th...
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of th...
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of th...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
Prion diseases are serious, not curable neurodegenerative disorders caused by the accumulation of th...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...