Synthesis and antiproliferative activity of a tetrahydrofuran analog of FR901464.

Bioorg Med Chem Lett

Department of Chemistry, University of Pittsburgh 219 Parkman Avenue, Pittsburgh, PA 15260, United States; Cancer Therapeutics Program, UPMC Hillman Cancer Center 5117 Centre Ave, Pittsburgh, PA 15232, United States. Electronic address:

Published: May 2024

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Article Abstract

FR901464 is a natural product that exhibits antiproliferative activity at single-digit nanomolar concentrations in cancer cells. Its tetrahydropyran-spiroepoxide covalently binds the spliceosome. Through our medicinal chemistry campaign, we serendipitously discovered that a bromoetherification formed a tetrahydrofuran. The tetrahydrofuran analog was three orders of magnitude less potent than the corresponding tetrahydropyran analogs. This study shows the significance of the tetrahydropyran ring that presents the epoxide toward the spliceosome.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11154589PMC
http://dx.doi.org/10.1016/j.bmcl.2024.129739DOI Listing

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