期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 26, 页码 6602-6616出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201307288
关键词
chemical synthesis; mutasynthesis; natural products; semisynthesis; thiopeptides
资金
- Spanish Science and Innovation Ministry, CICYT [CTQ2012-30930]
- Generalitat de Catalunya [2009SGR 1024]
- ISCIII
The recent development of thiopeptide analogues of antibiotics has allowed some of the limitations inherent to these naturally occurring substances to be overcome. Chemical synthesis, semisynthetic derivatization, and engineering of the biosynthetic pathway have independently led to complementary modifications of various thiopeptides. Some of the new substances have displayed improved profiles, not only as antibiotics, but also as antiplasmodial and anticancer drugs. The design of novel molecules based on the thiopeptide scaffold appears to be the only strategy to exploit the high potential they have shown in vitro. Herein we present the most relevant achievements in the production of thiopeptide analogues and also discuss the way the different approaches might be combined in a multidisciplinary strategy to produce more sophisticated structures.
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