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Spirotetronate Polyketides as Leads in Drug Discovery

[Image: see text] The discovery of chlorothricin (1) defined a new family of microbial metabolites with potent antitumor antibiotic properties collectively referred to as spirotetronate polyketides. These microbial metabolites are structurally distinguished by the presence of a spirotetronate motif...

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Autores principales: Lacoske, Michelle H., Theodorakis, Emmanuel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380204/
https://www.ncbi.nlm.nih.gov/pubmed/25434976
http://dx.doi.org/10.1021/np500757w
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author Lacoske, Michelle H.
Theodorakis, Emmanuel A.
author_facet Lacoske, Michelle H.
Theodorakis, Emmanuel A.
author_sort Lacoske, Michelle H.
collection PubMed
description [Image: see text] The discovery of chlorothricin (1) defined a new family of microbial metabolites with potent antitumor antibiotic properties collectively referred to as spirotetronate polyketides. These microbial metabolites are structurally distinguished by the presence of a spirotetronate motif embedded within a macrocyclic core. Glycosylation at the periphery of this core contributes to the structural complexity and bioactivity of this motif. The spirotetronate family displays impressive chemical structures, potent bioactivities, and significant pharmacological potential. This review groups the family members based on structural and biosynthetic considerations and summarizes synthetic and biological studies that aim to elucidate their mode of action and explore their pharmacological potential.
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spelling pubmed-43802042015-12-01 Spirotetronate Polyketides as Leads in Drug Discovery Lacoske, Michelle H. Theodorakis, Emmanuel A. J Nat Prod [Image: see text] The discovery of chlorothricin (1) defined a new family of microbial metabolites with potent antitumor antibiotic properties collectively referred to as spirotetronate polyketides. These microbial metabolites are structurally distinguished by the presence of a spirotetronate motif embedded within a macrocyclic core. Glycosylation at the periphery of this core contributes to the structural complexity and bioactivity of this motif. The spirotetronate family displays impressive chemical structures, potent bioactivities, and significant pharmacological potential. This review groups the family members based on structural and biosynthetic considerations and summarizes synthetic and biological studies that aim to elucidate their mode of action and explore their pharmacological potential. American Chemical Society and American Society of Pharmacognosy 2014-12-01 2015-03-27 /pmc/articles/PMC4380204/ /pubmed/25434976 http://dx.doi.org/10.1021/np500757w Text en Copyright © 2014 American Chemical Society and American Society of Pharmacognosy This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Lacoske, Michelle H.
Theodorakis, Emmanuel A.
Spirotetronate Polyketides as Leads in Drug Discovery
title Spirotetronate Polyketides as Leads in Drug Discovery
title_full Spirotetronate Polyketides as Leads in Drug Discovery
title_fullStr Spirotetronate Polyketides as Leads in Drug Discovery
title_full_unstemmed Spirotetronate Polyketides as Leads in Drug Discovery
title_short Spirotetronate Polyketides as Leads in Drug Discovery
title_sort spirotetronate polyketides as leads in drug discovery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380204/
https://www.ncbi.nlm.nih.gov/pubmed/25434976
http://dx.doi.org/10.1021/np500757w
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