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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.

DOI:10.1016/j.bmcl.2024.129739
PMID:38599298
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11154589/
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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本文引用的文献

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J Med Chem. 2023 Nov 9;66(21):14497-14512. doi: 10.1021/acs.jmedchem.3c00733. Epub 2023 Oct 23.
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Design and synthesis of 4-acetoxypentanamide derivatives of spliceostatin A and their biological evaluation towards prostate cancer treatment.拼接抑素 A 的 4-乙酰氧基戊酰胺衍生物的设计与合成及其对前列腺癌治疗的生物学评价。
Bioorg Med Chem Lett. 2023 Jul 15;91:129333. doi: 10.1016/j.bmcl.2023.129333. Epub 2023 May 18.
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Improved Synthesis of the Amine Fragment of FR901464 and Thailanstatins through the Development of a Convenient -Detosylation Method.
通过开发一种简便的脱对甲苯磺酰基方法改进FR901464和泰国他汀胺片段的合成
J Org Chem. 2022 Oct 7;87(19):13416-13421. doi: 10.1021/acs.joc.2c01889. Epub 2022 Sep 26.
4
Structural basis of intron selection by U2 snRNP in the presence of covalent inhibitors.U2 snRNP 结合共价抑制剂时对内含子选择的结构基础。
Nat Commun. 2021 Jul 23;12(1):4491. doi: 10.1038/s41467-021-24741-1.
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Design, Synthesis, and Biological Investigation of Thailanstatin A and Spliceostatin D Analogues Containing Tetrahydropyran, Tetrahydrooxazine, and Fluorinated Structural Motifs.泰兰他汀 A 和剪接体 D 类似物的设计、合成及含四氢吡喃、四氢恶嗪和氟化结构基序的生物研究。
J Org Chem. 2021 Feb 5;86(3):2499-2521. doi: 10.1021/acs.joc.0c02643. Epub 2021 Jan 8.
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