User profiles for Ugo Pradère

Ugo Pradere

Senior Scientist in Pharmaceutical Chemistry, ETH Zurich
Verified email at pharma.ethz.ch
Cited by 1491

A small-molecule inhibitor of Lin28

M Roos, U Pradère, RP Ngondo, A Behera… - ACS chemical …, 2016 - ACS Publications
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 …

[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 …

Novel antiviral C5-substituted pyrimidine acyclic nucleoside phosphonates selected as human thymidylate kinase substrates

D Topalis, U Pradere, V Roy, C Caillat… - Journal of medicinal …, 2011 - ACS Publications
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 …

Critical 23S rRNA interactions for macrolide-dependent ribosome stalling on the ErmCL nascent peptide chain

M Koch, J Willi, U Pradere, J Hall… - Nucleic acids …, 2017 - academic.oup.com
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 …

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-…

[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 …

Expeditious convergent procedure for the preparation of bis (POC) prodrugs of new (E)-4-phosphono-but-2-en-1-yl nucleosides

A Montagu, U Pradére, V Roy, SP Nolan, LA Agrofoglio - Tetrahedron, 2011 - Elsevier
A series of unsaturated acyclonucleoside bis(POC) prodrugs of E configuration were
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 …

Preparation of acyclo nucleoside phosphonate analogues based on cross-metathesis

H Kumamoto, D Topalis, J Broggi, U Pradere, V Roy… - Tetrahedron, 2008 - Elsevier
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 …

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 …