• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

CarbORev-5901:首个基于碳硼烷的5-脂氧合酶途径抑制剂。

CarbORev-5901: The First Carborane-Based Inhibitor of the 5-Lipoxygenase Pathway.

作者信息

Kuhnert Robert, Sárosi Menyhárt-Botond, George Sven, Lönnecke Peter, Hofmann Bettina, Steinhilber Dieter, Murganic Blagoje, Mijatovic Sanja, Maksimovic-Ivanic Danijela, Hey-Hawkins Evamarie

机构信息

Institut für Anorganische Chemie, Universität Leipzig, Johannisallee 29, 04103, Leipzig, Germany.

Institut für Pharmazeutische Chemie, Johann-Wolfgang-Goethe-Universität Frankfurt, Max-von-Laue-Straße 9, 60438, Frankfurt, Germany.

出版信息

ChemMedChem. 2017 Jul 6;12(13):1081-1086. doi: 10.1002/cmdc.201700309. Epub 2017 Jun 21.

DOI:10.1002/cmdc.201700309
PMID:28569429
Abstract

The progression of cancer is accelerated by increased proliferation, angiogenesis, and inflammation. These processes are mediated by leukotrienes. Several cancer cell lines overexpress 5-lipoxygenase, an enzyme that converts arachidonic acid into leukotrienes. An early inhibitor of the 5-lipoxygenase pathway is Rev-5901, which, however, lacks in in vivo efficacy, as it is rapidly metabolized. We investigated the introduction of carboranes as highly hydrophobic and metabolically stable pharmacophores into lipoxygenase inhibitors. Carboranes are icosahedral boron clusters that are remarkably stable and used to increase the metabolic stability of unstable pharmaceutics without changing their biological activity. By introduction of meta-carborane into Rev-5901, the first carborane-based inhibitor of the 5-lipoxygenase pathway was obtained. We report the synthesis and inhibitory and cytotoxic behavior of these compounds toward several melanoma and colon cancer cell lines and their related anticancer mechanisms.

摘要

增殖、血管生成和炎症增加会加速癌症进展。这些过程由白三烯介导。几种癌细胞系过度表达5-脂氧合酶,该酶可将花生四烯酸转化为白三烯。5-脂氧合酶途径的早期抑制剂是Rev-5901,然而,它缺乏体内疗效,因为它会迅速代谢。我们研究了将具有高疏水性和代谢稳定性的药效基团碳硼烷引入脂氧合酶抑制剂。碳硼烷是二十面体硼簇,非常稳定,用于增加不稳定药物的代谢稳定性而不改变其生物活性。通过将间碳硼烷引入Rev-5901,获得了首个基于碳硼烷的5-脂氧合酶途径抑制剂。我们报道了这些化合物对几种黑色素瘤和结肠癌细胞系的合成、抑制和细胞毒性行为及其相关的抗癌机制。

相似文献

1
CarbORev-5901: The First Carborane-Based Inhibitor of the 5-Lipoxygenase Pathway.CarbORev-5901:首个基于碳硼烷的5-脂氧合酶途径抑制剂。
ChemMedChem. 2017 Jul 6;12(13):1081-1086. doi: 10.1002/cmdc.201700309. Epub 2017 Jun 21.
2
Carborane-Based Analogues of 5-Lipoxygenase Inhibitors Co-inhibit Heat Shock Protein 90 in HCT116 Cells.硼烷类似物的 5-脂氧合酶抑制剂共同抑制 HCT116 细胞中的热休克蛋白 90
ChemMedChem. 2019 Jan 22;14(2):255-261. doi: 10.1002/cmdc.201800651. Epub 2018 Dec 21.
3
Borcalein: a Carborane-Based Analogue of Baicalein with 12-Lipoxygenase-Independent Toxicity.硼替佐米类似物:一种与 12-脂氧合酶无关的毒性的白杨素碳硼烷类似物。
ChemMedChem. 2022 Jan 5;17(1):e202100588. doi: 10.1002/cmdc.202100588. Epub 2021 Nov 11.
4
Discovery of a novel 2,5-dihydroxycinnamic acid-based 5-lipoxygenase inhibitor that induces apoptosis and may impair autophagic flux in RCC4 renal cancer cells.发现一种新型的 2,5-二羟基肉桂酸基 5-脂氧合酶抑制剂,可诱导 RCC4 肾癌细胞凋亡,并可能损害自噬流。
Eur J Med Chem. 2019 Oct 1;179:347-357. doi: 10.1016/j.ejmech.2019.06.060. Epub 2019 Jun 23.
5
[Pyrrolo(2,3-c)quinolines and pyrrolo(3,4-d)quinolines--synthesis and investigation of lipoxygenase inhibition].[吡咯并(2,3 - c)喹啉和吡咯并(3,4 - d)喹啉——脂氧合酶抑制作用的合成与研究]
Pharmazie. 2002 Apr;57(4):243-9.
6
Design, synthesis, and computational studies on dihydropyrimidine scaffolds as potential lipoxygenase inhibitors and cancer chemopreventive agents.作为潜在脂氧合酶抑制剂和癌症化学预防剂的二氢嘧啶支架的设计、合成及计算研究。
Drug Des Devel Ther. 2015 Feb 17;9:911-21. doi: 10.2147/DDDT.S73890. eCollection 2015.
7
Potent inhibition of human 5-lipoxygenase and microsomal prostaglandin E₂ synthase-1 by the anti-carcinogenic and anti-inflammatory agent embelin.抑癌抗炎剂 Embelin 对人 5-脂氧合酶和微粒体前列腺素 E₂ 合酶-1 的强效抑制作用。
Biochem Pharmacol. 2013 Aug 15;86(4):476-86. doi: 10.1016/j.bcp.2013.04.015. Epub 2013 Apr 24.
8
Discovery of novel hybrids of diaryl-1,2,4-triazoles and caffeic acid as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase for cancer therapy.发现新型二芳基-1,2,4-三唑与咖啡酸的杂合物作为环氧合酶-2和5-脂氧合酶的双重抑制剂用于癌症治疗。
Eur J Med Chem. 2016 Jan 27;108:89-103. doi: 10.1016/j.ejmech.2015.11.013. Epub 2015 Nov 11.
9
NMR metabolomics analysis of the effects of 5-lipoxygenase inhibitors on metabolism in glioblastomas.NMR 代谢组学分析 5-脂氧合酶抑制剂对神经胶质瘤代谢的影响。
J Proteome Res. 2013 May 3;12(5):2165-76. doi: 10.1021/pr400026q. Epub 2013 Apr 22.
10
Quinolines as potent 5-lipoxygenase inhibitors: synthesis and biological profile of L-746,530.
Bioorg Med Chem Lett. 1998 May 19;8(10):1255-60. doi: 10.1016/s0960-894x(98)00201-7.

引用本文的文献

1
Synthesis of Carborane-Thiazole Conjugates as Tyrosinase and 11β-Hydroxysteroid Dehydrogenase Inhibitors: Antiproliferative Activity and Molecular Docking Studies.硼烷噻唑缀合物的合成及其作为酪氨酸酶和 11β-羟甾脱氢酶抑制剂的研究:抗增殖活性和分子对接研究。
Molecules. 2024 Oct 5;29(19):4716. doi: 10.3390/molecules29194716.
2
Enhanced reversal of ABCG2-mediated drug resistance by replacing a phenyl ring in baicalein with a meta-carborane.米托蒽醌通过取代蒙达明中的苯环提高 ABCG2 介导的耐药逆转活性
Mol Oncol. 2024 Feb;18(2):280-290. doi: 10.1002/1878-0261.13527. Epub 2023 Oct 5.
3
The More the Better-Investigation of Polymethoxylated -Carboranyl Quinazolines as Novel Hybrid Breast Cancer Resistance Protein Inhibitors.
多多益善——多甲氧基化硼杂蒽并喹唑啉作为新型混合型乳腺癌耐药蛋白抑制剂的研究
Pharmaceutics. 2023 Jan 10;15(1):241. doi: 10.3390/pharmaceutics15010241.
4
Carborane-Based Analog of Rev-5901 Attenuates Growth of Colon Carcinoma In Vivo.基于碳硼烷的 Rev-5901 类似物可抑制结肠癌的体内生长。
Molecules. 2022 Jul 14;27(14):4503. doi: 10.3390/molecules27144503.
5
Boron-Containing Compounds for Prevention, Diagnosis, and Treatment of Human Metabolic Disorders.用于预防、诊断和治疗人类代谢紊乱的含硼化合物。
Biol Trace Elem Res. 2023 May;201(5):2222-2239. doi: 10.1007/s12011-022-03346-9. Epub 2022 Jun 30.
6
Carboranes as unique pharmacophores in antitumor medicinal chemistry.碳硼烷作为抗肿瘤药物化学中的独特药效基团。
Mol Ther Oncolytics. 2022 Jan 10;24:400-416. doi: 10.1016/j.omto.2022.01.005. eCollection 2022 Mar 17.
7
Borcalein: a Carborane-Based Analogue of Baicalein with 12-Lipoxygenase-Independent Toxicity.硼替佐米类似物:一种与 12-脂氧合酶无关的毒性的白杨素碳硼烷类似物。
ChemMedChem. 2022 Jan 5;17(1):e202100588. doi: 10.1002/cmdc.202100588. Epub 2021 Nov 11.
8
Ruthenacarborane and Quinoline: A Promising Combination for the Treatment of Brain Tumors.硼杂环戊二烯和喹啉:治疗脑肿瘤的有前途的组合。
Molecules. 2021 Jun 22;26(13):3801. doi: 10.3390/molecules26133801.