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doi:10.22028/D291-30944
Title: | Design and Synthesis of Bioisosteres of Acylhydrazones as Stable Inhibitors of the Aspartic Protease Endothiapepsin |
Author(s): | Jumde, Varsha R. Mondal, Milon Gierse, Robin M. Unver, M. Yagiz Magari, Francesca van Lier, Roos C. W. Heine, Andreas Klebe, Gerhard Hirsch, Anna |
Language: | English |
Title: | ChemMedChem : chemistry enabling drug discovery |
Volume: | 13 |
Issue: | 21 |
Startpage: | 2266 |
Endpage: | 2270 |
Publisher/Platform: | Wiley-VCH |
Year of Publication: | 2018 |
Publikation type: | Journal Article |
Abstract: | Acylhydrazone-based dynamic combinatorial chemistry (DCC) is a powerful strategy for the rapid identification of novel hits. Even though acylhydrazones are important structural motifs in medicinal chemistry, their further progression in development may be hampered by major instability and potential toxicity under physiological conditions. It is therefore of paramount importance to identify stable replacements for acylhydrazone linkers. Herein, we present the first report on the design and synthesis of stable bioisosteres of acylhydrazone-based inhibitors of the aspartic protease endothiapepsin as a follow-up to a DCC study. The most successful bioisostere is equipotent, bears an amide linker, and we confirmed its binding mode by X-ray crystallography. Having some validated bioisosteres of acylhydrazones readily available might accelerate hit-to-lead optimization in future acylhydrazone-based DCC projects. |
DOI of the first publication: | 10.1002/cmdc.201800446 |
URL of the first publication: | https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cmdc.201800446 |
Link to this record: | hdl:20.500.11880/29154 http://dx.doi.org/10.22028/D291-30944 |
ISSN: | 1860-7187 1860-7179 |
Date of registration: | 15-May-2020 |
Faculty: | NT - Naturwissenschaftlich- Technische Fakultät |
Department: | NT - Pharmazie |
Professorship: | NT - Prof. Dr. Anna Hirsch |
Collections: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
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