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Spirotetronate Polyketides as Leads in Drug Discovery
Author(s) -
Michelle H. Lacoske,
Emmanuel A. Theodorakis
Publication year - 2014
Publication title -
journal of natural products
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 139
eISSN - 1520-6025
pISSN - 0163-3864
DOI - 10.1021/np500757w
Subject(s) - drug discovery , structural motif , computational biology , biology , glycosylation , motif (music) , drug , biological activity , mode of action , common core , polyketide , chemistry , stereochemistry , biochemistry , pharmacology , core (optical fiber) , in vitro , biosynthesis , gene , materials science , acoustics , composite material , physics
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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