Allosteric Selectivity Design

Allosteric Selectivity Design is a methodological framework within off-target liability reduction that exploits allosteric binding sites to confer target specificity by modulating protein conformational dynamics in a manner distinct from orthosteric ligand interactions.

3

Publications

94

Citations

33

Authors

6

Institutions

Publications per year

2017–2026

1

Authors

33

  1. SV
    Steven V. O’Neil

    Pfizer (United States), United States

    1 publications · 44 citations

    1

    h-index

  2. MG
    Michael Green

    National Institute of Health Sciences, Japan

    1 publications · 44 citations

    1

    h-index

  3. RS
    Romelia Salomón–Ferrer

    Lawrence Berkeley National Laboratory, United States

    1 publications · 44 citations

    1

    h-index

  4. RS
    R. Scott Obach

    Pfizer (United States), United States

    1 publications · 44 citations

    1

    h-index

  5. SG
    Sarah Grimwood

    Pfizer (United States), United States

    1 publications · 44 citations

    1

    h-index

1–5 of 33

Venues

  1. European Journal of Medicinal Chemistry

    1 publications · 21 citations

    1

    h-index

  2. Molecular BioSystems

    1 publications · 29 citations

    1

    h-index

  3. Bioorganic & Medicinal Chemistry Letters

    1 publications · 44 citations

    1

    h-index

1–3