Tumor-selective Activation

Tumor-Selective Activation is a biopharmaceutical strategy within prodrug design that refers to the preferential enzymatic or chemical conversion of an inactive prodrug into its active cytotoxic form specifically within tumor tissues, thereby minimizing systemic toxicity and enhancing therapeutic efficacy.

64

Publications

4.3K

Citations

451

Authors

136

Institutions

Publications per year

2017–2026

17

Authors

451

  1. LH
    Laurence H. Patterson

    University of Bradford, United Kingdom

    3 publications · 114 citations

    3

    h-index

  2. LF
    Lutz F. Tietze

    University of Göttingen, Germany

    3 publications · 129 citations

    3

    h-index

  3. SD
    Steven D. Shnyder

    University of Bradford, United Kingdom

    3 publications · 114 citations

    3

    h-index

  4. KB
    Klaus Bosslet

    Behringwerke (Germany), Germany

    3 publications · 375 citations

    3

    h-index

  5. PM
    Paul M. Loadman

    University of Bradford, United Kingdom

    3 publications · 114 citations

    3

    h-index

1–5 of 451

Venues

  1. PubMed

    Repository · 9 publications · 621 citations

    9

    h-index

  2. Journal of Medicinal Chemistry

    5 publications · 326 citations

    5

    h-index

  3. Molecular Pharmaceutics

    3 publications · 93 citations

    3

    h-index

  4. Clinical Cancer Research

    3 publications · 316 citations

    3

    h-index

  5. Bioorganic & Medicinal Chemistry

    3 publications · 91 citations

    3

    h-index

1–5