Gpcr Selectivity

GPCR Selectivity is a pharmacological property that refers to the capacity of a ligand to preferentially bind to or activate a specific G protein-coupled receptor subtype over other structurally or functionally related GPCR subtypes.

181

Publications

12.9K

Citations

1.3K

Authors

363

Institutions

Publications per year

2017–2026

71

Variants

G Protein-coupled Receptor Selectivity

Authors

1.3K

  1. GM
    Graeme Milligan

    University of Glasgow, United Kingdom

    10 publications · 497 citations

    10

    h-index

  2. DE
    David E. Gloriam

    University of Copenhagen, Denmark

    10 publications · 1.2K citations

    10

    h-index

  3. MB
    Michel Bouvier

    Université de Montréal, Canada

    9 publications · 784 citations

    9

    h-index

  4. AS
    Alexander S. Hauser

    University of Copenhagen, Denmark

    6 publications · 752 citations

    6

    h-index

  5. AI
    Asuka Inoue

    Tohoku University, Japan

    5 publications · 1K citations

    5

    h-index

1–5 of 1.3K

Venues

  1. Journal of Medicinal Chemistry

    17 publications · 977 citations

    15

    h-index

  2. Journal of Biological Chemistry

    JBC · 8 publications · 693 citations

    8

    h-index

  3. Molecular Pharmacology

    7 publications · 322 citations

    7

    h-index

  4. Proceedings of the National Academy of Sciences

    PNAS · 7 publications · 510 citations

    7

    h-index

  5. Journal of Chemical Information and Modeling

    JCIM · 5 publications · 150 citations

    5

    h-index

1–5