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Fragment‐Based Drug Design Facilitated by Protein‐Templated Click Chemistry: Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin

There is an urgent need for the development of efficient methodologies that accelerate drug discovery. We demonstrate that the strategic combination of fragment linking/optimization and protein‐templated click chemistry is an efficient and powerful method that accelerates the hit‐identification proc...

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Detalhes bibliográficos
Publicado no:Chemistry
Main Authors: Mondal, Milon, Unver, M. Yagiz, Pal, Asish, Bakker, Matthijs, Berrier, Stephan P., Hirsch, Anna K. H.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5095814/
https://ncbi.nlm.nih.gov/pubmed/27604032
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/chem.201603001
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