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Michal Hocek

Researcher Next ID · RN-041346

Researcher · Biochemistry, Genetics and Molecular Biology

Charles University

Prague, Poland

Accepting doctoral researchersFunding unknown
Works count
631
Citation count
10,568
H-index
55
i10-index
251

Research interests

Biochemistry, Genetics and Molecular Biology
Materials Science
Medicine
DNA and Nucleic Acid Chemistry
Advanced biosensing and bioanalysis techniques
HIV/AIDS drug development and treatment
Crystallization and Solubility Studies
X-ray Diffraction in Crystallography

Publications

  • Enzymatic Synthesis of Base-Functionalized Nucleic Acids for Sensing, Cross-linking, and Modulation of Protein–DNA Binding and Transcription

    Accounts of Chemical Research · 2019 · 10.1021/acs.accounts.9b00195

  • Pyrrolo[2,3‐ d ]pyrimidine (7‐deazapurine) as a privileged scaffold in design of antitumor and antiviral nucleosides

    Medicinal Research Reviews · 2017 · 10.1002/med.21465

  • Pyrrolo[2,3‐ d ]pyrimidine (7‐deazapurine) as a privileged scaffold in design of antitumor and antiviral nucleosides

    Medicinal Research Reviews · 2017 · 10.1002/med.21465

  • A Rotational BODIPY Nucleotide: An Environment‐Sensitive Fluorescence‐Lifetime Probe for DNA Interactions and Applications in Live‐Cell Microscopy

    Angewandte Chemie International Edition · 2015 · 10.1002/anie.201507922

  • A Rotational BODIPY Nucleotide: An Environment‐Sensitive Fluorescence‐Lifetime Probe for DNA Interactions and Applications in Live‐Cell Microscopy

    Angewandte Chemie International Edition · 2015 · 10.1002/anie.201507922

  • Inside Cover: A Rotational BODIPY Nucleotide: An Environment‐Sensitive Fluorescence‐Lifetime Probe for DNA Interactions and Applications in Live‐Cell Microscopy (Angew. Chem. Int. Ed. 1/2016)

    Angewandte Chemie International Edition · 2015 · 10.1002/anie.201510985

  • Synthesis of Base-Modified 2′-Deoxyribonucleoside Triphosphates and Their Use in Enzymatic Synthesis of Modified DNA for Applications in Bioanalysis and Chemical Biology

    The Journal of Organic Chemistry · 2014 · 10.1021/jo5020799

  • Systematic exploration of a class of hydrophobic unnatural base pairs yields multiple new candidates for the expansion of the genetic alphabet

    Nucleic Acids Research · 2014 · 10.1093/nar/gku715

  • Synthesis of Base-Modified 2′-Deoxyribonucleoside Triphosphates and Their Use in Enzymatic Synthesis of Modified DNA for Applications in Bioanalysis and Chemical Biology

    The Journal of Organic Chemistry · 2014 · 10.1021/jo5020799

  • Vinylsulfonamide and Acrylamide Modification of DNA for Cross‐linking with Proteins

    Angewandte Chemie International Edition · 2013 · 10.1002/anie.201303577

  • Nucleobase modification as redox DNA labelling for electrochemical detection

    Chemical Society Reviews · 2011 · 10.1039/c1cs15049a

  • Nucleobase modification as redox DNA labelling for electrochemical detection

    Chemical Society Reviews · 2011 · 10.1039/c1cs15049a

  • Synthesis and Significant Cytostatic Activity of 7-Hetaryl-7-deazaadenosines

    Journal of Medicinal Chemistry · 2011 · 10.1021/jm2005173

  • Synthesis and Photophysical Properties of Biaryl-Substituted Nucleos(t)ides. Polymerase Synthesis of DNA Probes Bearing Solvatochromic and pH-Sensitive Dual Fluorescent and 19 F NMR Labels

    The Journal of Organic Chemistry · 2011 · 10.1021/jo202321g

  • Direct Polymerase Synthesis of Reactive Aldehyde‐Functionalized DNA and Its Conjugation and Staining with Hydrazines

    Angewandte Chemie International Edition · 2009 · 10.1002/anie.200905556

  • C -Nucleosides: Synthetic Strategies and Biological Applications

    Chemical Reviews · 2009 · https://doi.org/10.1021/cr9002165

  • Aminophenyl‐ and Nitrophenyl‐Labeled Nucleoside Triphosphates: Synthesis, Enzymatic Incorporation, and Electrochemical Detection

    Angewandte Chemie International Edition · 2008 · 10.1002/anie.200705088

  • Cross-coupling reactions of nucleoside triphosphates followed by polymerase incorporation. Construction and applications of base-functionalized nucleic acids

    Organic & Biomolecular Chemistry · 2008 · 10.1039/b803664k

  • Aminophenyl‐ and Nitrophenyl‐Labeled Nucleoside Triphosphates: Synthesis, Enzymatic Incorporation, and Electrochemical Detection

    Angewandte Chemie International Edition · 2008 · 10.1002/anie.200705088

  • Cross-coupling reactions of nucleoside triphosphates followed by polymerase incorporation. Construction and applications of base-functionalized nucleic acids

    Organic & Biomolecular Chemistry · 2008 · 10.1039/b803664k

  • Base‐Modified DNA Labeled by [Ru(bpy)3]2+ and [Os(bpy)3]2+ Complexes: Construction by Polymerase Incorporation of Modified Nucleoside Triphosphates, Electrochemical and Luminescent Properties, and Applications

    Chemistry - A European Journal · 2008 · 10.1002/chem.200801538

  • An Efficient Method for the Construction of Functionalized DNA Bearing Amino Acid Groups through Cross‐Coupling Reactions of Nucleoside Triphosphates Followed by Primer Extension or PCR

    Chemistry - A European Journal · 2007 · 10.1002/chem.200700220

  • Ferrocenylethynyl Derivatives of Nucleoside Triphosphates: Synthesis, Incorporation, Electrochemistry, and Bioanalytical Applications

    Chemistry - A European Journal · 2007 · 10.1002/chem.200701249

  • An Efficient Method for the Construction of Functionalized DNA Bearing Amino Acid Groups through Cross‐Coupling Reactions of Nucleoside Triphosphates Followed by Primer Extension or PCR

    Chemistry - A European Journal · 2007 · 10.1002/chem.200700220

  • Ferrocenylethynyl Derivatives of Nucleoside Triphosphates: Synthesis, Incorporation, Electrochemistry, and Bioanalytical Applications

    Chemistry - A European Journal · 2007 · 10.1002/chem.200701249

  • Direct C−H Arylation of Purines: Development of Methodology and Its Use in Regioselective Synthesis of 2,6,8-Trisubstituted Purines

    Organic Letters · 2006 · 10.1021/ol062324j

  • Direct C−H Arylation of Purines: Development of Methodology and Its Use in Regioselective Synthesis of 2,6,8-Trisubstituted Purines

    Organic Letters · 2006 · 10.1021/ol062324j

  • Cross-coupling reactions of unprotected halopurine bases, nucleosides, nucleotides and nucleoside triphosphates with 4-boronophenylalanine in water. Synthesis of (purin-8-yl)- and (purin-6-yl)phenylalanines

    Organic & Biomolecular Chemistry · 2006 · 10.1039/b604010a

  • Cytostatic 6-Arylpurine Nucleosides. 6. SAR in Anti-HCV and Cytostatic Activity of Extended Series of 6-Hetarylpurine Ribonucleosides

    Journal of Medicinal Chemistry · 2005 · 10.1021/jm050335x

  • Cytostatic 6-Arylpurine Nucleosides. 6. SAR in Anti-HCV and Cytostatic Activity of Extended Series of 6-Hetarylpurine Ribonucleosides

    Journal of Medicinal Chemistry · 2005 · 10.1021/jm050335x

  • An Efficient Synthesis of 2-Substituted 6-Methylpurine Bases and Nucleosides by Fe- or Pd-Catalyzed Cross-Coupling Reactions of 2,6-Dichloropurines

    The Journal of Organic Chemistry · 2003 · 10.1021/jo034351i

  • Syntheses of Purines Bearing Carbon Substituents in Positions 2, 6 or 8 by Metal‐ or Organometal‐Mediated C−C Bond‐Forming Reactions

    European Journal of Organic Chemistry · 2002 · 10.1002/ejoc.200390025

  • Syntheses of Purines Bearing Carbon Substituents in Positions 2, 6 or 8 by Metal‐ or Organometal‐Mediated C−C Bond‐Forming Reactions

    European Journal of Organic Chemistry · 2002 · 10.1002/ejoc.200390025

  • Cytostatic 6-Arylpurine Nucleosides III. Synthesis and Structure-Activity Relationship Study in Cytostatic Activity of 6-Aryl-, 6-Hetaryl- and 6-Benzylpurine Ribonucleosides

    Collection of Czechoslovak Chemical Communications · 2001 · 10.1135/cccc20010483

  • Synthesis and Cytostatic Activity of Substituted 6-Phenylpurine Bases and Nucleosides: Application of the Suzuki−Miyaura Cross-Coupling Reactions of 6-Chloropurine Derivatives with Phenylboronic Acids

    Journal of Medicinal Chemistry · 2000 · https://doi.org/10.1021/jm991167+

Current projects

    No projects listed.