Milan Kožíšek

Institute of Organic Chemistry and Biochemistry

Czech Republic

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Articles (16)

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2025

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2025

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2025

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2025

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2024

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2021

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2021

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2021

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2021

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2021

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2020

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2020

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2020

Collaborators (4)

Ales Machara

Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry

CZECH REPUBLIC

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Zahra Aliakbar Tehrani

Institute of Biotechnology

CZECH REPUBLIC

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Jakub Zýka

University of Chemistry and Technology

CZECH REPUBLIC

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Zdenek Vavrina

Institute of Organic Chemistry and Biochemistry

CZECH REPUBLIC

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Milan Kožíšek

Research Interests

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Articles (16)

The evaluation of DNA-linked inhibitor antibody and AlphaScreen assays for high-throughput screening of compounds targeting the cap-binding domain in influenza a polymerase

Design of Potent Mannose‐6‐Phosphate Derivatives as Ligands for CI‐M6P/IGF2R Using Fluorescence Polarization Assay

3′‐Dehydroxypurpurogallin‐4‐Carboxamides as Influenza A Endonuclease Inhibitors: Synthesis, Structure–Activity Relationship Analysis, and Structural Characterization of Protein Complex

Design of Zn‐Binding Peptide(s) from Protein Fragments

Front Cover: 3’‐Dehydroxypurpurogallin‐4‐Carboxamides as Influenza A Endonuclease Inhibitors: Synthesis, Structure‐Activity Relationship Analysis, and Structural Characterization of Protein Complex (ChemMedChem 3/2025)

3’‐Dehydroxypurpurogallin‐4‐carboxamides as Influenza A Endonuclease Inhibitors: Synthesis, SAR Analysis, and Structural Characterization of Protein Complex

Apollon: a deoxyribozyme that generates a yellow product

Thermodynamic and structural characterization of an optimized peptide-based inhibitor of the influenza polymerase PA-PB1 subunit interaction

Ligand Strain and Its Conformational Complexity Is a Major Factor in the Binding of Cyclic Dinucleotides to STING Protein

Ligand Strain and Its Conformational Complexity Is a Major Factor Determining Binding of Cyclic Dinucleotides to STING Protein.

Protein-Ligand Interactions in the STING Binding Site Probed by Rationally Designed Single-Point Mutations: Experiment and Theory.

Synthesis and In Vitro Evaluation of C-7 and C-8 Luteolin Derivatives as Influenza Endonuclease Inhibitors

Structural and Thermodynamic Analysis of the Resistance Development to Pimodivir (VX-787), the Clinical Inhibitor of Cap Binding to PB2 Subunit of Influenza A Polymerase

Structural characterization of the interaction between the C-terminal domain of the influenza polymerase PA subunit and an optimized small peptide inhibitor.

Unraveling the anti-influenza effect of flavonoids: Experimental validation of luteolin and its congeners as potent influenza endonuclease inhibitors.

Rhomboid intramembrane protease YqgP licenses bacterial membrane protein quality control as adaptor of FtsH AAA protease.

Collaborators (4)

Ales Machara

Zahra Aliakbar Tehrani

Jakub Zýka

Zdenek Vavrina

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