Front Cover: SAR Studies of the Leupyrrins: Design and Total Synthesis of Highly Potent Simplified Leupylogs (Chem. Eur. J. 66/2020)

The design and total synthesis of dramatically simplified leupylogs is presented. They demonstrate similar highly potent antifungal activities as the natural leupyrrins, as depicted by a balanced IC50 weighing scale. The origin of the secondary metabolites from the myxobacterium Sorangium cellulosum...

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Veröffentlicht in:Chemistry : a European journal 2020-11, Vol.26 (66), p.15047-15047
Hauptverfasser: Wosniok, Paul R., Knopf, Christopher, Dreisigacker, Sandra, Orozco‐Rodriguez, J. Manuel, Hinkelmann, Bettina, Mueller, Peter P., Brönstrup, Mark, Menche, Dirk
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container_end_page 15047
container_issue 66
container_start_page 15047
container_title Chemistry : a European journal
container_volume 26
creator Wosniok, Paul R.
Knopf, Christopher
Dreisigacker, Sandra
Orozco‐Rodriguez, J. Manuel
Hinkelmann, Bettina
Mueller, Peter P.
Brönstrup, Mark
Menche, Dirk
description The design and total synthesis of dramatically simplified leupylogs is presented. They demonstrate similar highly potent antifungal activities as the natural leupyrrins, as depicted by a balanced IC50 weighing scale. The origin of the secondary metabolites from the myxobacterium Sorangium cellulosum is illustrated by its fruiting bodies while the flask portrays the synthetic endeavors which have led to the discovery of leupylogs. More information can be found in the Communication by D. Menche et al. on page 15074.
doi_str_mv 10.1002/chem.202003844
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subjects antifungal agents
Leupylogs
natural products
SAR studies
total synthesis
title Front Cover: SAR Studies of the Leupyrrins: Design and Total Synthesis of Highly Potent Simplified Leupylogs (Chem. Eur. J. 66/2020)
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