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.
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886
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222
Institutions
Publications per year
2017–2026
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Brian E. Huber, Elizabeth A. Austin, C A Richards et al. · Proceedings of the National Academy of Sciences · 1994 · 422 citations
Medicine, Oncology, Pharmacology +17
Single‐Triggered Trimeric Prodrugs
Keren Haba, Mikhail Popkov, Marina Shamis et al. · Angewandte Chemie International Edition · 2005 · 158 citations · Full text
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Institute of Biomedical Sciences, Academia Sinica, Taiwan
4 publications · 136 citations
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Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry, Czechia
3 publications · 124 citations
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Tel Aviv University
Tel Aviv, Israel
5 h-index
18 publications
1K citations
University of Kansas
Lawrence, United States
4 h-index
13 publications
389 citations
University of Michigan
Ann Arbor, United States
4 h-index
15 publications
310 citations
Scripps Research Institute
San Diego, United States
4 h-index
15 publications
921 citations

Johns Hopkins University
Baltimore, United States
4 h-index
32 publications
1.4K citations
Chia Nan University of Pharmacy and Science
Tainan City, Taiwan
3 h-index
15 publications
415 citations
University of Oxford
Oxford, United Kingdom
3 h-index
6 publications
325 citations
Rega Institute for Medical Research
Leuven, Belgium
3 h-index
4 publications
330 citations
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28 publications · 1.6K citations
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Repository · 11 publications · 715 citations
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8 publications · 243 citations
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6 publications · 142 citations
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