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SAR Studies of the Leupyrrins: Design and Total Synthesis of Highly Potent Simplified Leupylogs.

Wosniok, Paul R
; 
Knopf, Christopher
; 
Dreisigacker, Sandra
; 
Orozco-Rodriguez, J Manuel
; 
Hinkelmann, Bettina
; 
Mueller, Peter P
; ; 
Menche, Dirk
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Issue Date
2020-11-11
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Abstract
Invited for the cover of this issue is the group of Dirk Menche at the University of Bonn. The image depicts the natural product leupyrrin A1 and a synthetic leupylog in balance on an IC50 weighing scale. Read the full text of the article at 10.1002/chem.202002622.
Citation
Chemistry. 2020 Nov 11. doi: 10.1002/chem.202003845. Epub ahead of print.
Affiliation
HZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany.
Publisher
Wiley
Journal
Chemistry (Weinheim an der Bergstrasse, Germany)
URI
http://hdl.handle.net/10033/622586
DOI
10.1002/chem.202003845
PubMed ID
33174290
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Article
Language
en
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1521-3765
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Attribution-NonCommercial-ShareAlike 4.0 International
cbn
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Publications of the research group Chemical Biology (CBIO)