Publications
- Rational Design of Highly Potent SARS-CoV-2 nsp14 Methyltransferase Inhibitors2023 | Faculty of Science, Central Library of Charles University
- Exploring positions 6 and 7 of a quinazoline-based scaffold leads to changes in selectivity and potency towards RIPK2/3 kinases2023 | Faculty of Science, Central Library of Charles University
- Discovery of isonucleotidic CDNs as potent STING agonists with immunomodulatory potential2022 | Faculty of Science, Central Library of Charles University
- Structure-based design and modular synthesis of novel PI4K class II inhibitors bearing a 4-aminoquinazoline scaffold2022 | Faculty of Science, Central Library of Charles University
- High-Throughput Fluorescent Assay for Inhibitor Screening of Proteases from RNA Viruses2021 | Central Library of Charles University
- Non-Nucleotide RNA-Dependent RNA Polymerase Inhibitor That Blocks SARS-CoV-2 Replication2021 | Central Library of Charles University
- Enzymatic Preparation of 2′–5′,3′–5′-Cyclic Dinucleotides, Their Binding Properties to Stimulator of Interferon Genes Adaptor Protein, and Structure/Activity Correlations2019 | Faculty of Science, Central Library of Charles University
- The structural model of Zika virus RNA-dependent RNA polymerase in complex with RNA for rational design of novel nucleotide inhibitors2018 | Central Library of Charles University
- Highly Selective Phosphatidylinositol 4-Kinase III beta Inhibitors and Structural Insight into Their Mode of Action2015 | Central Library of Charles University
- The high-resolution crystal structure of phosphatidylinositol 4-kinase IIβ and the crystal structure of phosphatidylinositol 4-kinase IIα containing a nucleoside analogue provide a structural basis for isoform-specific inhibitor design2015 | Central Library of Charles University
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