Prion diseases are fatal neurodegenerative disorders that affect humans and animals and for which no pharmacological treatment is available. Compounds consisting of two identical moieties joined via an appropriate spacer (i.e. bivalent compounds) have turned out to be effective tools to prevent prion fibril formation and exhibit an improved biological profile with regard to the corresponding monovalent derivatives. In this review we discuss the importance of the bivalent strategy as a viable approach to design new chemical entities to combat prion diseases
<div><p>The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
Prion diseases are fatal neurodegenerative disorders caused by protein misfolding and aggregation, a...
Prion diseases are fatal neurodegenerative disorders that affect humans and animals and for which no...
Prion diseases, or transmissible spongiform encephalopathies (TSEs), are neurodegenerative and infec...
A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting two ...
Prion diseases are prototypical conformational diseases. From a medicinal chemistry point of view, a...
A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting two ...
none7A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
none2noTherapy of prion diseases represents an extremely challenging effort for scientists working i...
ABSTRACTPrion diseases are a group of incurable zoonotic neurodegenerative diseases (NDDs) in humans...
Prion diseases (PrDs) are fatal neurodegenerative disorders, for which no effective therapeutic and ...
Background: The main pathogenic event of prion disorders has been identified in the deposition of th...
Prion diseases are associated with the conversion of the cellular prion protein (PrPC), a glycoprote...
<div><p>The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
Prion diseases are fatal neurodegenerative disorders caused by protein misfolding and aggregation, a...
Prion diseases are fatal neurodegenerative disorders that affect humans and animals and for which no...
Prion diseases, or transmissible spongiform encephalopathies (TSEs), are neurodegenerative and infec...
A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting two ...
Prion diseases are prototypical conformational diseases. From a medicinal chemistry point of view, a...
A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting two ...
none7A library of 11 entries, featuring a 2,5-diamino-1,4-benzoquinones nucleus as spacer connecting...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
none2noTherapy of prion diseases represents an extremely challenging effort for scientists working i...
ABSTRACTPrion diseases are a group of incurable zoonotic neurodegenerative diseases (NDDs) in humans...
Prion diseases (PrDs) are fatal neurodegenerative disorders, for which no effective therapeutic and ...
Background: The main pathogenic event of prion disorders has been identified in the deposition of th...
Prion diseases are associated with the conversion of the cellular prion protein (PrPC), a glycoprote...
<div><p>The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs...
The prion protein (PrP) is implicated in the Transmissible Spongiform Encephalopathies (TSEs), which...
Prion diseases are fatal neurodegenerative disorders caused by protein misfolding and aggregation, a...