Fragment-based Discovery

Fragment-Based Discovery is a drug discovery approach that identifies low molecular weight chemical fragments binding weakly but efficiently to target proteins, which are subsequently optimized into high-affinity ligands through iterative structural and medicinal chemistry refinement.

768

Publications

38.1K

Citations

4.8K

Authors

978

Institutions

Publications per year

2017–2026

308

Authors

4.8K

  1. CA
    Chris Abell

    University of Cambridge, United Kingdom

    24 publications · 1.5K citations

    21

    h-index

  2. TL
    Tom L. Blundell

    University of Cambridge, United Kingdom

    19 publications · 878 citations

    16

    h-index

  3. CW
    Christopher W. Murray

    Proteus (United Kingdom), United Kingdom

    15 publications · 1.9K citations

    15

    h-index

  4. RE
    Roderick E. Hubbard

    University of York, United Kingdom

    14 publications · 714 citations

    14

    h-index

  5. IJ
    Iwan J. P. de Esch

    Vrije Universiteit Amsterdam, Netherlands

    12 publications · 695 citations

    12

    h-index

1–5 of 4.8K

Venues

  1. Journal of Medicinal Chemistry

    158 publications · 11.5K citations

    64

    h-index

  2. Journal of Chemical Information and Modeling

    JCIM · 40 publications · 1.4K citations

    25

    h-index

  3. Bioorganic & Medicinal Chemistry Letters

    34 publications · 1.4K citations

    24

    h-index

  4. ACS Medicinal Chemistry Letters

    28 publications · 1.2K citations

    21

    h-index

  5. Journal of the American Chemical Society

    JACS · 20 publications · 1.8K citations

    20

    h-index

1–5