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利用葫芦[7]脲的主体-客体化学抑制孔雀石绿对人肝细胞的毒性。

Suppression of Malachite Green-Induced Toxicity to Human Liver Cells Utilizing Host-Guest Chemistry of Cucurbit[7]uril.

机构信息

Institute of Industrial Science, The University of Tokyo, 4-6-1 Komaba, Meguro, Tokyo, 153-8505, Japan.

出版信息

Anal Sci. 2021 Mar 10;37(3):525-528. doi: 10.2116/analsci.20SCN02. Epub 2020 Nov 20.

DOI:10.2116/analsci.20SCN02
PMID:33229827
Abstract

We investigated a host-guest complex between cucurbit[7]uril and malachite green, and its effect on the toxicity to human liver cells. The host-guest complexation was evaluated by a UV/vis titration and electrospray-ionization mass spectrometry. Interestingly, the host-guest complex resulted in remarkable suppression of the toxicity of malachite green in its practical concentration range (ca. ∼6 μM). This study is one step forward to the active control of the biological effects of potent toxicants utilizing host-guest chemistry.

摘要

我们研究了葫芦[7]脲与孔雀石绿之间的主客体配合物及其对人肝细胞毒性的影响。通过紫外/可见滴定和电喷雾电离质谱评估了主客体络合作用。有趣的是,在实际浓度范围内(约 6 μM),主客体复合物显著抑制了孔雀石绿的毒性。这项研究朝着利用主客体化学主动控制强毒性物质的生物学效应迈出了一步。

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Suppression of Malachite Green-Induced Toxicity to Human Liver Cells Utilizing Host-Guest Chemistry of Cucurbit[7]uril.利用葫芦[7]脲的主体-客体化学抑制孔雀石绿对人肝细胞的毒性。
Anal Sci. 2021 Mar 10;37(3):525-528. doi: 10.2116/analsci.20SCN02. Epub 2020 Nov 20.
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J Org Chem. 2018 Apr 20;83(8):4882-4887. doi: 10.1021/acs.joc.8b00543. Epub 2018 Apr 6.
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本文引用的文献

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New class of artificial enzyme composed of Mn-porphyrin, imidazole, and cucurbit[10]uril toward use as a therapeutic antioxidant.由锰卟啉、咪唑和葫芦[10]脲组成的新型人工酶用作治疗性抗氧化剂。
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Noninnocent Role of Na Ions in the Binding of the N-Phenyl-2-naphthylammonium Cation as a Ditopic Guest with Cucurbit[7]uril.
钠离子在 N-苯基-2-萘基铵阳离子作为双位点客体与环七硅氧烷的结合中的非无辜角色。
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Nanomolar Binding of Steroids to Cucurbit[n]urils: Selectivity and Applications.类固醇与葫芦脲的纳摩尔结合:选择性和应用。
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Cytotoxicity Regulated by Host-Guest Interactions: A Supramolecular Strategy to Realize Controlled Disguise and Exposure.受主体-客体相互作用调控的细胞毒性:一种实现控制伪装和暴露的超分子策略。
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Supramolecular Inhibition of Neurodegeneration by a Synthetic Receptor.合成受体对神经退行性变的超分子抑制作用
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