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甲氨蝶呤与其光开关衍生物异构体清除作用的比较电子顺磁共振研究

Comparative EPR Study on the Scavenging Effect of Methotrexate with the Isomers of Its Photoswitchable Derivative.

作者信息

Preisz Zsolt, Hartvig Nóra, Bognár Balázs, Kálai Tamás, Kunsági-Máté Sándor

机构信息

Institute of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Pécs, Szigeti 12, H-7624 Pécs, Hungary.

Department of General and Physical Chemistry, Faculty of Sciences, University of Pécs, Ifjúság 6, H-7624 Pécs, Hungary.

出版信息

Pharmaceuticals (Basel). 2021 Jul 11;14(7):665. doi: 10.3390/ph14070665.

Abstract

The scavenging effect of the antimetabolite dihydrofolate reductase inhibitor methotrexate (MTX) and the isomers of its photoswitchable derivate, - and -phototrexate (PHX), have been compared by ESR spectroscopy, with the application of a cyclic hydroxylamine spin probe. The results showed the most pronounced scavenging effect in the presence of -phototrexate (-PHX). At a low concentration (100 µM) -PHX also showed a greater scavenging effect than the parent molecule MTX. Direct antioxidant properties of the investigated molecules were measured by ABTS scavenging assay, which showed no significant difference between -PHX and -PHX, but both of the isomers of PHX showed a higher antioxidant capacity than MTX. These findings imply that -PHX may have more pronounced anti-inflammatory and tissue-protective effects than MTX, despite the lack of its cytotoxic, antineoplastic effect.

摘要

通过电子自旋共振光谱法,应用环状羟胺自旋探针,比较了抗代谢物二氢叶酸还原酶抑制剂甲氨蝶呤(MTX)及其光开关衍生物的异构体α-和β-光甲氨蝶呤(PHX)的清除作用。结果表明,在α-光甲氨蝶呤(α-PHX)存在的情况下,清除作用最为明显。在低浓度(100μM)时,α-PHX的清除作用也比母体分子MTX更强。通过ABTS清除试验测定了所研究分子的直接抗氧化性能,结果表明α-PHX和β-PHX之间没有显著差异,但两种PHX异构体的抗氧化能力均高于MTX。这些发现表明,尽管α-PHX缺乏细胞毒性和抗肿瘤作用,但它可能比MTX具有更明显的抗炎和组织保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2bb/8308517/9365fa865252/pharmaceuticals-14-00665-g001.jpg

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