% IMPORTANT: The following is UTF-8 encoded. This means that in the presence % of non-ASCII characters, it will not work with BibTeX 0.99 or older. % Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or % “biber”. @ARTICLE{Bongarzone:201266, author = {Bongarzone, Salvatore and Tran, Hoang Ngoc Ai and Cavalli, Andrea and Roberti, Marinella and Carloni, Paolo and Legname, Giuseppe and Bolognesi, Maria Laura}, title = {{P}arallel {S}ynthesis, {E}valuation, and {P}reliminary {S}tructure−{A}ctivity {R}elationship of 2,5-{D}iamino-1,4-benzoquinones as a {N}ovel {C}lass of {B}ivalent {A}nti-{P}rion {C}ompound}, journal = {Journal of medicinal chemistry}, volume = {53}, number = {22}, issn = {1520-4804}, address = {Washington, DC}, publisher = {ACS}, reportid = {FZJ-2015-03571}, pages = {8197 - 8201}, year = {2010}, abstract = {A 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 EC50 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.}, cin = {GRS / IAS-5}, ddc = {540}, cid = {I:(DE-Juel1)GRS-20100316 / I:(DE-Juel1)IAS-5-20120330}, pnm = {899 - ohne Topic (POF2-899)}, pid = {G:(DE-HGF)POF2-899}, typ = {PUB:(DE-HGF)16}, UT = {WOS:000284287200029}, doi = {10.1021/jm100882t}, url = {https://juser.fz-juelich.de/record/201266}, }