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用于靶向体内硝基还原酶可视化的荧光探针的合理设计。

Rational design of fluorescent probes for targeted in vivo nitroreductase visualization.

机构信息

School of Pharmacy & Minhang Hospital, Fudan University, Shanghai 201301, China.

出版信息

Org Biomol Chem. 2020 Jul 1;18(25):4744-4747. doi: 10.1039/d0ob00082e.

Abstract

Nitroreductase (NTR) has been recognized as a biomarker for identifying the hypoxic status of cancers. Therefore, it is of high scientific interest to design effective fluorescent probes for tracking NTR activity. However, studies on elucidation of the structure-performance relationship of fluorescent probes and those providing valuable insight into optimized probe design have rarely been reported. Three BODIPY based fluorescent probes were made by conjugation of para-, ortho-, and meta-nitrobenzene to the BODIPY core via a thiolether bond, respectively. Our study revealed that the linkage and nitro substituent position significantly influence the capability of nitroreductase detection.

摘要

硝基还原酶(NTR)已被认为是一种生物标志物,可用于识别癌症的缺氧状态。因此,设计用于跟踪 NTR 活性的有效荧光探针具有很高的科学意义。然而,关于荧光探针的结构-性能关系的研究以及为优化探针设计提供有价值见解的研究很少有报道。通过硫醚键将对硝基苯、邻硝基苯和间硝基苯分别连接到 BODIPY 核心上,合成了三种基于 BODIPY 的荧光探针。我们的研究表明,连接方式和硝基取代基位置对硝基还原酶检测能力有显著影响。

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