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Piet Herdewijn

Researcher Next ID · RN-039452

Researcher · Biochemistry, Genetics and Molecular Biology

PLA Information Engineering University

Zhengzhou, Belgium

Accepting doctoral researchersFunding unknown
Works count
1,161
Citation count
24,294
H-index
73
i10-index
474

Research interests

Biochemistry, Genetics and Molecular Biology
Chemistry
Medicine
DNA and Nucleic Acid Chemistry
HIV/AIDS drug development and treatment
Advanced biosensing and bioanalysis techniques
Carbohydrate Chemistry and Synthesis
RNA and protein synthesis mechanisms

Publications

  • Anticancer kinase inhibitors impair intracellular viral trafficking and exert broad-spectrum antiviral effects

    Journal of Clinical Investigation · 2017 · 10.1172/jci89857

  • Catalysts from synthetic genetic polymers

    Nature · 2014 · 10.1038/nature13982

  • Mutations in the chikungunya virus non-structural proteins cause resistance to favipiravir (T-705), a broad-spectrum antiviral

    Journal of Antimicrobial Chemotherapy · 2014 · 10.1093/jac/dku209

  • Synthetic Genetic Polymers Capable of Heredity and Evolution

    Science · 2012 · https://doi.org/10.1126/science.1217622

  • Chemical Evolution of a Bacterium’s Genome

    Angewandte Chemie International Edition · 2011 · 10.1002/anie.201100535

  • A screen of chemical modifications identifies position-specific modification by UNA to most potently reduce siRNA off-target effects

    Nucleic Acids Research · 2010 · https://doi.org/10.1093/nar/gkq341

  • Toward Safe Genetically Modified Organisms through the Chemical Diversification of Nucleic Acids

    Chemistry & Biodiversity · 2009 · 10.1002/cbdv.200900083

  • A large-scale chemical modification screen identifies design rules to generate siRNAs with high activity, high stability and low toxicity

    Nucleic Acids Research · 2009 · https://doi.org/10.1093/nar/gkp106

  • α- l -ribo-Configured Locked Nucleic Acid (α-L-LNA): Synthesis and Properties

    Journal of the American Chemical Society · 2002 · 10.1021/ja0168763

  • Cyclohexene Nucleic Acids (CeNA): Serum Stable Oligonucleotides that Activate RNase H and Increase Duplex Stability with Complementary RNA

    Journal of the American Chemical Society · 2000 · 10.1021/ja000018+

  • Modifications in Lignin and Accumulation of Phenolic Glucosides in Poplar Xylem upon Down-regulation of Caffeoyl-Coenzyme A O-Methyltransferase, an Enzyme Involved in Lignin Biosynthesis

    Journal of Biological Chemistry · 2000 · 10.1074/jbc.m006915200

  • Exploring the active site of herpes simplex virus type-1 thymidine kinase by X-ray crystallography of complexes with aciclovir and other ligands

    Proteins Structure Function and Bioinformatics · 1998 · 10.1002/(sici)1097-0134(19980815)32:3<350::aid-prot10>3.0.co;2-8

  • Characterization of Synthetic Human Granulocyte Chemotactic Protein 2: Usage of Chemokine Receptors CXCR1 and CXCR2 andin VivoInflammatory Properties

    Biochemistry · 1997 · 10.1021/bi961999z

  • Synthesis and antiherpes virus activity of 1,5-anhydrohexitol nucleosides

    Journal of Medicinal Chemistry · 1993 · 10.1021/jm00066a013

  • Intracellular metabolism and mechanism of anti-retrovirus action of 9-(2-phosphonylmethoxyethyl)adenine, a potent anti-human immunodeficiency virus compound.

    Proceedings of the National Academy of Sciences · 1991 · 10.1073/pnas.88.4.1499

  • Marked in vivo antiretrovirus activity of 9-(2-phosphonylmethoxyethyl)adenine, a selective anti-human immunodeficiency virus agent.

    Proceedings of the National Academy of Sciences · 1989 · 10.1073/pnas.86.1.332

  • Differential Patterns of Intracellular Metabolism of 2′,3′-Didehydro-2′,3′-dideoxythymidine and 3′-Azido-2′,3′-dideoxythymidine, Two Potent Anti-human Immunodeficiency Virus Compounds

    Journal of Biological Chemistry · 1989 · https://doi.org/10.1016/s0021-9258(18)83322-1

  • Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds

    Journal of Virological Methods · 1988 · https://doi.org/10.1016/0166-0934(88)90134-6

  • Anti-retrovirus activity of 3′-fluoro- and 3′-azido-substituted pyrimidine 2′,3′-dideoxynucleoside analogues

    Biochemical Pharmacology · 1988 · 10.1016/0006-2952(88)90049-4

  • The in vitro and in vivo anti-retrovirus activity, and intracellular metabolism of 3′-azido-2′,3′-dideoxythymidine and 2′,3′-dideoxycytidine are highly dependent on the cell species

    Biochemical Pharmacology · 1988 · 10.1016/0006-2952(88)90178-5

  • Ribavirin antagonizes inhibitory effects of pyrimidine 2',3'-dideoxynucleosides but enhances inhibitory effects of purine 2',3'-dideoxynucleosides on replication of human immunodeficiency virus in vitro

    Antimicrobial Agents and Chemotherapy · 1987 · 10.1128/aac.31.10.1613

  • Sensitive and rapid assay on MT-4 cells for detection of antiviral compounds against the AIDS virus

    Journal of Virological Methods · 1987 · 10.1016/0166-0934(87)90002-4

  • Both 2′,3′-dideoxythymidine and its 2′,3′-unsaturated derivative (2′,3′-dideoxythymidinene) are potent and selective inhibitors of human immunodeficiency virus replication in vitro

    Biochemical and Biophysical Research Communications · 1987 · https://doi.org/10.1016/0006-291x(87)90460-8

  • 3'-Substituted 2',3'-dideoxynucleoside analogs as potential anti-HIV (HTLV-III/LAV) agents

    Journal of Medicinal Chemistry · 1987 · 10.1021/jm00391a003

  • The anti-HTLV-III (anti-HIV) and cytotoxic activity of 2',3'-didehydro-2',3'-dideoxyribonucleosides: a comparison with their parental 2',3'-dideoxyribonucleosides.

    Molecular Pharmacology · 1987 · 10.1016/s0026-895x(25)13752-8

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