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Versatile Synthetic Route to Cycloheximide and Analogues That Potently Inhibit Translation Elongation.
- Source :
-
Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2019 Apr 08; Vol. 58 (16), pp. 5387-5391. Date of Electronic Publication: 2019 Mar 19. - Publication Year :
- 2019
-
Abstract
- Cycloheximide (CHX) is an inhibitor of eukaryotic translation elongation that has played an essential role in the study of protein synthesis. Despite its ubiquity, few studies have been directed towards accessing synthetic CHX derivatives, even though such efforts may lead to protein synthesis inhibitors with improved or alternate properties. Described here is the total synthesis of CHX and analogues, and the establishment of structure-activity relationships (SAR) responsible for translation inhibition. The SAR studies aided the design of more potent compounds, one of which irreversibly blocks ribosomal elongation, preserves polysome profiles, and may be a broadly useful tool for investigating protein synthesis.<br /> (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)
- Subjects :
- Biological Products chemical synthesis
Biological Products chemistry
Cycloheximide chemical synthesis
Cycloheximide chemistry
Dose-Response Relationship, Drug
Eukaryotic Cells metabolism
Molecular Conformation
Protein Biosynthesis drug effects
Ribosomes metabolism
Structure-Activity Relationship
Biological Products pharmacology
Cycloheximide pharmacology
Eukaryotic Cells drug effects
Ribosomes drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1521-3773
- Volume :
- 58
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- Angewandte Chemie (International ed. in English)
- Publication Type :
- Academic Journal
- Accession number :
- 30802354
- Full Text :
- https://doi.org/10.1002/anie.201901386