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Chemical Biology
Cyclic Peptides: From Bioorganic Synthesis to Applications
Edited by
Jesko Koehnke;
Jesko Koehnke
Helmholtz Centre for Infection Research, Germany
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Wilfred A van der Donk
Wilfred A van der Donk
University of Illinois, USA
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Hardback ISBN:
978-1-78262-528-5
PDF ISBN:
978-1-78801-015-3
EPUB ISBN:
978-1-78801-377-2
Special Collection:
2017 ebook collection
Series:
Chemical Biology
No. of Pages:
380
Published online:
14 Dec 2017
Published in print:
15 Dec 2017
Book Chapter
CHAPTER 6: Biology and Synthesis of the Argyrins
By
L. Millbrodt
;
L. Millbrodt
Leibniz Universität Hannover, Institute for Organic Chemistry
Schneiderberg 1B
30167 Hannover
Germany
Centre of Biomolecular Drug Research (BMWZ)
Schneiderberg 38
30167 Hannover
Germany
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M. Kalesse
M. Kalesse
Leibniz Universität Hannover, Institute for Organic Chemistry
Schneiderberg 1B
30167 Hannover
Germany
Centre of Biomolecular Drug Research (BMWZ)
Schneiderberg 38
30167 Hannover
Germany
Helmholtz Zentrum für Infektionsforschung (HZI)
Inhoffenstr 7
38124 Braunschweig
Germany
[email protected]
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Published:14 Dec 2017
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Special Collection: 2017 ebook collectionSeries: Chemical Biology
Page range:
122 - 140
Citation
L. Millbrodt and M. Kalesse, in Cyclic Peptides: From Bioorganic Synthesis to Applications, ed. J. Koehnke, J. Naismith, and W. A. van der Donk, The Royal Society of Chemistry, 2017, pp. 122-140.
Download citation file:
Argyrins A–F, isolated in 2002, are non-ribosomal cyclic peptides exhibiting a unique framework. Their remarkable bioactivity includes antibiotic, immunosuppressive and antitumor properties. The explanation of their properties can be found in the inhibition of bacterial elongation factor G and p27kip1 inhibition. Synthetic studies towards argyrins A–F have been investigated by four groups using different novel pathways of polypeptide chemistry in three convergent approaches and one linear solid-phase peptide synthesis.
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