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四氢呋喃类似物 FR901464 的合成及抗增殖活性。

Synthesis and antiproliferative activity of a tetrahydrofuran analog of FR901464.

机构信息

Department of Chemistry, University of Pittsburgh 219 Parkman Avenue, Pittsburgh, PA 15260, United States.

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.

出版信息

Bioorg Med Chem Lett. 2024 May 15;104:129739. doi: 10.1016/j.bmcl.2024.129739. Epub 2024 Apr 8.

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.

摘要

FR901464 是一种天然产物,在癌细胞中以个位数纳摩尔浓度表现出抗增殖活性。其四氢吡喃-螺环环氧乙烷通过共价键与剪接体结合。通过我们的药物化学研究,我们偶然发现溴醚化形成了四氢呋喃。四氢呋喃类似物的效力比相应的四氢吡喃类似物低三个数量级。这项研究表明了四氢吡喃环的重要性,它使环氧乙烷朝向剪接体。

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Synthesis and antiproliferative activity of a tetrahydrofuran analog of FR901464.四氢呋喃类似物 FR901464 的合成及抗增殖活性。
Bioorg Med Chem Lett. 2024 May 15;104:129739. doi: 10.1016/j.bmcl.2024.129739. Epub 2024 Apr 8.

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