Fragment-based Selectivity Design

Fragment-Based Selectivity Design is a fragment-based drug design strategy that specifically optimizes molecular fragments for selective target engagement by minimizing interactions with off-target proteins, thereby enhancing therapeutic precision.

18

Publications

681

Citations

157

Authors

41

Institutions

Publications per year

2017–2026

8

Authors

157

  1. AU
    Andrea Unzue

    University of Zurich, Switzerland

    2 publications · 137 citations

    2

    h-index

  2. JD
    Jing Dong

    Chinese Academy of Fishery Sciences, China

    2 publications · 137 citations

    2

    h-index

  3. MX
    Min Xu

    Dalian Medical University, China

    2 publications · 137 citations

    2

    h-index

  4. CN
    Cristina Nevado

    University of Zurich, Switzerland

    2 publications · 137 citations

    2

    h-index

  5. AC
    Amedeo Caflisch

    University of Zurich, Switzerland

    2 publications · 137 citations

    2

    h-index

1–5 of 157

Venues

  1. Journal of Medicinal Chemistry

    6 publications · 295 citations

    6

    h-index

  2. Bioorganic & Medicinal Chemistry

    2 publications · 80 citations

    2

    h-index

  3. Bioorganic & Medicinal Chemistry Letters

    2 publications · 96 citations

    2

    h-index

  4. European Journal of Medicinal Chemistry

    2 publications · 27 citations

    2

    h-index

  5. Chemical Communications

    ChemComm · 1 publications · 20 citations

    1

    h-index

1–5