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Synthesis and antiproliferative activity of a tetrahydrofuran analog of FR901464.
Pohorilets, Ivanna; Beard, Jacob P; Driscoll, Julia L; Schmitz, John C; Koide, Kazunori.
Affiliation
  • Pohorilets I; Department of Chemistry, University of Pittsburgh 219 Parkman Avenue, Pittsburgh, PA 15260, United States.
  • Beard JP; Department of Chemistry, University of Pittsburgh 219 Parkman Avenue, Pittsburgh, PA 15260, United States.
  • Driscoll JL; Department of Chemistry, University of Pittsburgh 219 Parkman Avenue, Pittsburgh, PA 15260, United States.
  • Schmitz JC; Division of Hematology-Oncology, Department of Medicine, University of Pittsburgh School of Medicine 5150 Centre Avenue, Pittsburgh, PA 15232, United States; Cancer Therapeutics Program, UPMC Hillman Cancer Center 5117 Centre Ave, Pittsburgh, PA 15232, United States.
  • Koide K; 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: koide@pitt.edu.
Bioorg Med Chem Lett ; 104: 129739, 2024 May 15.
Article in En | MEDLINE | ID: mdl-38599298
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrans / Spiro Compounds / Epoxy Compounds / Furans Limits: Humans Language: En Journal: Bioorg Med Chem Lett Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyrans / Spiro Compounds / Epoxy Compounds / Furans Limits: Humans Language: En Journal: Bioorg Med Chem Lett Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Type: Article Affiliation country: United States