Michal Hocek
Researcher Next ID · RN-041346
Researcher · Biochemistry, Genetics and Molecular Biology
Prague, Poland
- Works count
- 631
- Citation count
- 10,568
- H-index
- 55
- i10-index
- 251
Research interests
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
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