Fragment Linking and Optimization of Inhibitors of the Aspartic Protease Endothiapepsin: Fragment‐Based Drug Design Facilitated by Dynamic Combinatorial Chemistry

Fragment‐based drug design (FBDD) affords active compounds for biological targets. While there are numerous reports on FBDD by fragment growing/optimization, fragment linking has rarely been reported. Dynamic combinatorial chemistry (DCC) has become a powerful hit‐identification strategy for biologi...

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Detalles Bibliográficos
Autores principales: Mondal, Milon, Radeva, Nedyalka, Fanlo‐Virgós, Hugo, Otto, Sijbren, Klebe, Gerhard, Hirsch, Anna K. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113778/
https://www.ncbi.nlm.nih.gov/pubmed/27400756
http://dx.doi.org/10.1002/anie.201603074

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113778/
https://www.ncbi.nlm.nih.gov/pubmed/27400756
http://dx.doi.org/10.1002/anie.201603074

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