Fragment-based Selectivity Design
Fragment-Based Selectivity Design is a fragment-based drug design strategy that specifically optimizes molecular fragments for selective target engagement by minimizing interactions with off-target proteins, thereby enhancing therapeutic precision.
18
Publications
681
Citations
157
Authors
41
Institutions
Publications per year
2017–2026
8
18
Selectivity of Kinase Inhibitor Fragments
Paul Bamborough, Murray J. B. Brown, J.A. Christopher et al. · Journal of Medicinal Chemistry · 2011 · 66 citations · Full text
Fragment-Based Design of Selective Nanomolar Ligands of the CREBBP Bromodomain
Andrea Unzue, Min Xu, Jing Dong et al. · Journal of Medicinal Chemistry · 2015 · 62 citations · Full text
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41
University of Zurich
Zurich, Switzerland
2 h-index
13 publications
884 citations
Xavier University of Louisiana
New Orleans, United States
1 h-index
2 publications
60 citations

Centre National de la Recherche Scientifique
Paris, France
1 h-index
1 publications
26 citations

Universidade Federal do ABC
Santo André, Brazil
1 h-index
1 publications
11 citations
University of Cambridge
Cambridge, United Kingdom
1 h-index
7 publications
476 citations

University of Bath
Bath, United Kingdom
1 h-index
2 publications
96 citations
Wellcome Centre for Infectious Diseases Research in Africa
Cape Town, South Africa
1 h-index
3 publications
144 citations
Tolero Pharmaceuticals (United States)
Lehi, United States
1 h-index
4 publications
64 citations
1–8 of 41
6 publications · 295 citations
6
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2 publications · 80 citations
2
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2 publications · 96 citations
2
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2 publications · 27 citations
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ChemComm · 1 publications · 20 citations
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