Fragmentverknüpfung und ‐optimierung von Hemmstoffen der Aspartylprotease Endothiapepsin: Fragmentbasiertes Wirkstoffdesign beschleunigt durch dynamische kombinatorische Chemie-Reference-Cited by-同舟云学术

Fragmentverknüpfung und ‐optimierung von Hemmstoffen der Aspartylprotease Endothiapepsin: Fragmentbasiertes Wirkstoffdesign beschleunigt durch dynamische kombinatorische Chemie

Published:2016-07-12 Issue:32 Volume:128 Page:9569-9574
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Mondal Milon¹^ORCID,Radeva Nedyalka²,Fanlo‐Virgós Hugo³^ORCID,Otto Sijbren³,Klebe Gerhard²^ORCID,Hirsch Anna K. H.¹^ORCID

Affiliation:

1. Stratingh Institute for ChemistryUniversity of Groningen Nijenborgh 7 9747 AG Groningen Niederlande

2. Institute of Pharmaceutical Chemistry Marbach Weg 6 35032 Marburg Deutschland

3. Centre for Systems Chemistry, Stratingh Institute for ChemistryUniversity of Groningen Nijenborgh 4 9747 AG Groningen Niederlande

Funder

Dutch Ministry of Education, Culture, Science

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201603074

Reference41 articles.

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5. Introduction to Fragment-Based Drug Discovery

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