Prodrug Selectivity

Prodrug Selectivity is a pharmacological property that denotes the preferential activation or conversion of a prodrug into its active metabolite at the target site or within the target population, distinguishing it from non-selective prodrug activation by virtue of its spatial, temporal, or biochemical specificity.

143

Publications

6.3K

Citations

886

Authors

222

Institutions

Publications per year

2017–2026

31

Authors

886

  1. AN
    Abraham Nudelman

    Bar-Ilan University, Israel

    4 publications · 156 citations

    4

    h-index

  2. SR
    Steve R. Roffler

    Institute of Biomedical Sciences, Academia Sinica, Taiwan

    4 publications · 136 citations

    4

    h-index

  3. AR
    Ada Rephaeli

    Bar-Ilan University, Israel

    4 publications · 156 citations

    4

    h-index

  4. KB
    Kenneth B. Sloan

    University of Florida, United States

    3 publications · 40 citations

    3

    h-index

  5. PM
    Pavel Majer

    Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry, Czechia

    3 publications · 124 citations

    3

    h-index

1–5 of 886

Venues

  1. Journal of Medicinal Chemistry

    28 publications · 1.6K citations

    24

    h-index

  2. PubMed

    Repository · 11 publications · 715 citations

    11

    h-index

  3. Bioorganic & Medicinal Chemistry Letters

    8 publications · 243 citations

    8

    h-index

  4. Molecules

    6 publications · 92 citations

    6

    h-index

  5. Journal of Pharmaceutical Sciences

    6 publications · 142 citations

    6

    h-index

1–5