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.
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4.3K
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451
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136
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2017–2026
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Stefan W. Krause, Robert Gastpar, Reinhard Andreesen et al. · Clinical Cancer Research · 2004 · 242 citations · Full text
Life Sciences, Immunology, Oncology +17
Elucidation of the mechanism enabling tumor selective prodrug monotherapy.
Klaus Bosslet, Rainer H. Straub, Matthias Blumrich et al. · PubMed · 1998 · 226 citations
Medicine, Oncology, Pharmacology +13
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136

University of Bradford
Bradford, United Kingdom
4 h-index
31 publications
1.2K citations

Chinese Academy of Sciences
Beijing, China
3 h-index
6 publications
224 citations

University of Göttingen
Göttingen, Germany
3 h-index
13 publications
671 citations

Chinese Academy of Medical Sciences & Peking Union Medical College
Beijing, China
2 h-index
7 publications
134 citations

Peking University
Beijing, China
2 h-index
9 publications
783 citations
Center for Life Sciences
Beijing, China
2 h-index
5 publications
367 citations
Shanghai Institutes for Biological Sciences
Shanghai, China
2 h-index
3 publications
182 citations
Institute of Biomedical Sciences, Academia Sinica
Taipei, Taiwan
2 h-index
7 publications
213 citations
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Repository · 9 publications · 621 citations
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5 publications · 326 citations
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3 publications · 93 citations
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3 publications · 316 citations
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3 publications · 91 citations
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