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Morten Meldal

Researcher Next ID · RN-038876

Researcher · Biochemistry, Genetics and Molecular Biology

University of Copenhagen

Copenhagen, Denmark

Accepting doctoral researchersFunding unknown
Works count
480
Citation count
24,494
H-index
59
i10-index
239

Research interests

Biochemistry, Genetics and Molecular Biology
Chemistry
Medicine
Chemical Synthesis and Analysis
Carbohydrate Chemistry and Synthesis
Glycosylation and Glycoproteins Research
Click Chemistry and Applications
Monoclonal and Polyclonal Antibodies Research

Publications

  • Recent Fascinating Aspects of the CuAAC Click Reaction

    Trends in Chemistry · 2020 · 10.1016/j.trechm.2020.03.007

  • A comparative study of the physicochemical properties of iron isomaltoside 1000 (Monofer®), a new intravenous iron preparation and its clinical implications

    European Journal of Pharmaceutics and Biopharmaceutics · 2011 · 10.1016/j.ejpb.2011.03.016

  • Maintaining Biological Activity by Using Triazoles as Disufide Bond Mimetics

    Angewandte Chemie International Edition · 2011 · 10.1002/anie.201005846

  • Cu-Catalyzed Azide−Alkyne Cycloaddition

    Chemical Reviews · 2008 · https://doi.org/10.1021/cr0783479

  • Polymer “Clicking” by CuAAC Reactions

    Macromolecular Rapid Communications · 2008 · https://doi.org/10.1002/marc.200800159

  • Combinatorial Library of Peptidotriazoles: Identification of [1,2,3]-Triazole Inhibitors against a Recombinant Leishmania m exicana Cysteine Protease

    Journal of Combinatorial Chemistry · 2004 · 10.1021/cc020085v

  • Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

    The Journal of Organic Chemistry · 2002 · https://doi.org/10.1021/jo011148j

  • Peptidotriazoles: Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions on Solid-Phase

    · 2001 · 10.1007/978-94-010-0464-0_119

  • Internally quenched fluorescent peptide substrates disclose the subsite preferences of human caspases 1, 3, 6, 7 and 8

    Biochemical Journal · 2000 · https://doi.org/10.1042/bj3500563

  • SPOCC: A Resin for Solid-Phase Organic Chemistry and Enzymatic Reactions on Solid Phase

    Journal of the American Chemical Society · 1999 · 10.1021/ja984355i

  • POEPOP and POEPS: Inert polyethylene glycol crosslinked polymeric supports for solid synthesis

    Tetrahedron Letters · 1996 · 10.1016/0040-4039(96)01319-6

  • Portion-mixing peptide libraries of quenched fluorogenic substrates for complete subsite mapping of endoprotease specificity.

    Proceedings of the National Academy of Sciences · 1994 · 10.1073/pnas.91.8.3314

  • A PEGA resin for use in the solid-phase chemical–enzymatic synthesis of glycopeptides

    Journal of the Chemical Society Chemical Communications · 1994 · 10.1039/c39940001849

  • Substrate preferences of glutamic‐acid‐specific endopeptidases assessed by synthetic Peptide Substrates based on intramolecular fluorescence quenching

    European Journal of Biochemistry · 1992 · 10.1111/j.1432-1033.1992.tb16906.x

  • Extensive comparison of the substrate preferences of two subtilisins as determined with peptide substrates which are based on the principle of intramolecular quenching

    Biochemistry · 1992 · 10.1021/bi00141a008

  • Pega: a flow stable polyethylene glycol dimethyl acrylamide copolymer for solid phase synthesis.

    Tetrahedron Letters · 1992 · https://doi.org/10.1016/s0040-4039(00)79604-3

  • Anthranilamide and nitrotyrosine as a donor-acceptor pair in internally quenched fluorescent substrates for endopeptidases: Multicolumn peptide synthesis of enzyme substrates for subtilisin carlsberg and pepsin

    Analytical Biochemistry · 1991 · 10.1016/0003-2697(91)90309-h

Current projects

    No projects listed.