User profiles for Ugo Pradère
Ugo PradereSenior Scientist in Pharmaceutical Chemistry, ETH Zurich Verified email at pharma.ethz.ch Cited by 1491 |
A small-molecule inhibitor of Lin28
New discoveries in RNA biology underscore a need for chemical tools to clarify their roles in
pathophysiological mechanisms. In certain cancers, synthesis of the let-7 microRNA tumor …
pathophysiological mechanisms. In certain cancers, synthesis of the let-7 microRNA tumor …
[HTML][HTML] Synthesis of nucleoside phosphate and phosphonate prodrugs
U Pradere, EC Garnier-Amblard, SJ Coats… - Chemical …, 2014 - ACS Publications
For many decades, the design of new nucleoside analogs as potential therapeutic agents
focused on both sugar and nucleobase modifications. These nucleoside analogs rely on …
focused on both sugar and nucleobase modifications. These nucleoside analogs rely on …
Novel antiviral C5-substituted pyrimidine acyclic nucleoside phosphonates selected as human thymidylate kinase substrates
Acyclic nucleoside phosphonates (ANPs) are at the cornerstone of DNA virus and retrovirus
therapies. They reach their target, the viral DNA polymerase, after two phosphorylation steps …
therapies. They reach their target, the viral DNA polymerase, after two phosphorylation steps …
Critical 23S rRNA interactions for macrolide-dependent ribosome stalling on the ErmCL nascent peptide chain
The nascent peptide exit tunnel has recently been identified as a functional region of
ribosomes contributing to translation regulation and co-translational protein folding. Inducible …
ribosomes contributing to translation regulation and co-translational protein folding. Inducible …
Preparation of ribavirin analogues by copper-and ruthenium-catalyzed azide-alkyne 1, 3-dipolar cycloaddition
U Pradere, V Roy, TR McBrayer, RF Schinazi… - Tetrahedron, 2008 - Elsevier
In this study, we described the synthesis of 1,4- and 1,5-disubstituted-1,2,3-triazolo-nucleosides
from various alkynes with 1′-azido-2′,3′,5′-tri-O-acetylribose using either copper-…
from various alkynes with 1′-azido-2′,3′,5′-tri-O-acetylribose using either copper-…
[HTML][HTML] The solution structure of Dead End bound to AU-rich RNA reveals an unusual mode of tandem RRM-RNA recognition required for mRNA regulation
…, FE Loughlin, C von Schroetter, U Pradère… - Nature …, 2022 - nature.com
Dead End (DND1) is an RNA-binding protein essential for germline development through
its role in post-transcriptional gene regulation. The molecular mechanisms behind selection …
its role in post-transcriptional gene regulation. The molecular mechanisms behind selection …
Expeditious convergent procedure for the preparation of bis (POC) prodrugs of new (E)-4-phosphono-but-2-en-1-yl nucleosides
A series of unsaturated acyclonucleoside bis(POC) prodrugs of E configuration were
synthesized through an expeditious, highly efficient and stereoselective one-step procedure from …
synthesized through an expeditious, highly efficient and stereoselective one-step procedure from …
Short loop-targeting oligoribonucleotides antagonize Lin28 and enable pre-let-7 processing and suppression of cell growth in let-7-deficient cancer cells
…, M Lucic, D Pavlicek, U Pradere… - Nucleic acids …, 2015 - academic.oup.com
MicroRNAs (miRNAs) originate from stem-loop-containing precursors (pre-miRNAs, pri-miRNAs)
and mature by means of the Drosha and Dicer endonucleases and their associated …
and mature by means of the Drosha and Dicer endonucleases and their associated …
Preparation of acyclo nucleoside phosphonate analogues based on cross-metathesis
In our on-going program targeting anti-pox activity, we report here the synthesis of hitherto
unknown acyclic nucleoside phosphonates using olefin cross-metathesis (CM) as a key …
unknown acyclic nucleoside phosphonates using olefin cross-metathesis (CM) as a key …
β-d-2′-C-Methyl-2,6-diaminopurine Ribonucleoside Phosphoramidates are Potent and Selective Inhibitors of Hepatitis C Virus (HCV) and Are Bioconverted …
…, M Ehteshami, S Amiralaei, U Pradere… - Journal of medicinal …, 2015 - ACS Publications
The conversion of selected β-d-2,6-diaminopurine nucleosides (DAPNs) to their phosphoramidate
prodrug (PD) substantially blocks the conversion to the G-analog allowing for the …
prodrug (PD) substantially blocks the conversion to the G-analog allowing for the …