Myriaporone 3/4 structure--activity relationship studies define a pharmacophore targeting eukaryotic protein synthesis

• Published in: Molecular bioSystems Vol. 2; no. 8; p. 371
• Main Authors: Hines, John, Roy, Myriam, Cheng, Hua, Agapakis, Christina M, Taylor, Richard, Crews, Craig M
• Format: Journal Article
• Language: English
• Published: England 01.08.2006
• Subjects: Animals; Anti-Infective Agents - chemistry; Anti-Infective Agents - pharmacology; Antineoplastic Agents - chemistry; Antineoplastic Agents - pharmacology; Aorta - cytology; Cattle; Cell Proliferation - drug effects; Cells, Cultured; Dose-Response Relationship, Drug; Endothelial Cells - drug effects; Epoxy Compounds - agonists; Epoxy Compounds - chemical synthesis; Epoxy Compounds - chemistry; Epoxy Compounds - pharmacology; Escherichia coli - drug effects; Mammals; Models, Biological; Protein Biosynthesis - drug effects; Pyrans - agonists; Pyrans - chemistry; Pyrans - pharmacology; Structure-Activity Relationship; Yeasts - drug effects
• ISSN: 1742-206X
• DOI: 10.1039/b602936a

Myriaporones are naturally occurring compounds which structurally resemble the southern hemisphere of the tedanolide family of macrolide antitumor agents. Despite the fact that myriaporone 3/4 represents only a portion of tedanolide, it nonetheless retains much of its biological activity. We show here that like tedanolide, myriaporone 3/4 inhibits protein synthesis and proliferation of mammalian cells with low nanomolar potencies but displays no prokaryotic growth inhibitory effect. Moreover, myriaporone 3/4 displays a very rapid, reversible and p21-independent activity to block S phase progression in mammalian cells. Structure-activity relationship studies revealed that the C18-C19 epoxide and the C14 hydroxymethyl group (tedanolide numbering) of myriaporone 3/4 are required for cell cycle inhibition. These constitute previously unidentified and/or novel pharmacophores for myriaporone 3/4. Our results show that the important biological activities associated with the structurally complex tedanolides are present and can be harnessed in the chemically much simpler myriaporones. This greatly increases the value of the latter as investigative tools for biochemical research as well as for development of potential therapeutics.