Conjugation Reactions

Conjugation Reactions is a class of phase II biotransformation reactions in drug metabolism in which a xenobiotic or its metabolite is covalently linked to an endogenous, usually activated, polar moiety (such as glucuronic acid, sulfate, acetate, amino acids, or glutathione), thereby forming more hydrophilic and typically less pharmacologically active products that are more readily eliminated.

6.6K

Publications

306.4K

Citations

21.8K

Authors

3.3K

Institutions

Publications per year

2017–2026

762

Authors

21.8K

  1. PJ
    Peter J. van Bladeren

    Wageningen University & Research, Netherlands

    24 publications · 1.9K citations

    22

    h-index

  2. BM
    Bengt Mannervik

    Uppsala University, Sweden

    20 publications · 2.5K citations

    19

    h-index

  3. KM
    Keiji Maruoka

    Kyoto University, Japan

    20 publications · 1.1K citations

    18

    h-index

  4. GJ
    Gerard J. Mulder

    Leiden University, Netherlands

    19 publications · 753 citations

    16

    h-index

  5. AA
    Alexandre Alexakis

    University of Geneva, Switzerland

    16 publications · 2.2K citations

    16

    h-index

1–5 of 21.8K

Venues

  1. Journal of the American Chemical Society

    JACS · 367 publications · 25.9K citations

    90

    h-index

  2. The Journal of Organic Chemistry

    JOC · 475 publications · 18.3K citations

    64

    h-index

  3. Bioconjugate Chemistry

    165 publications · 8.3K citations

    51

    h-index

  4. Tetrahedron Letters

    380 publications · 11.9K citations

    50

    h-index

  5. Journal of Biological Chemistry

    JBC · 107 publications · 25K citations

    49

    h-index

1–5