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  • 學位論文

硝基還原酶螢光探針的合成路徑探討

Exploration of synthetic routes for Nitroreductase fluorescent probe

指導教授 : 黃聲東

摘要


硝基還原酶(NTR)是細菌中一種已知的黃素酶,可以催化硝基芳香化合物形成胺基芳香化合物的還原反應,硝基還原酶被廣泛使用生物醫藥、抗菌劑等,也可以應用在檢測含硝基芳香化合物的環境汙染物。檢測硝基還原酶的方法很多,常見的是利用螢光分子探針,但多數螢光探針是溶解性較差,因此設計一個溶解性較好的新隱藏式螢光探針NBF-L來即時偵測硝基還原酶的活性,隱藏式螢光探針在未活化可以穩定存在,僅在特一的化學反應有強烈的螢光釋出,且為不可逆的反應,但是在合成隱藏式螢光探針NBF-L的過程中,結果不如預期,從此進行研究探討。

並列摘要


Nitroreductase (NTR) is a flavoenzyme with β-nicotinamide adenine dinucleotide (NADH) or β-nicotinamide adenine dinucleotide phosphate (NADPH) as a cofactor. NTR catalyzes the reduction of nitro compound to correspond in amine. The use of fluorescent probes assists real-time detection of NTR for hypoxia. We prepare a new long-wavelength latent fluorogenic probe, NBF-L, for the monitoring NRT activities. The fluorogenic probes are stable that unmask their intense fluorescence only by a user-designated chemical reaction, and they are especially useful tools for basic research in the biological sciences. The fluorogenic chemical transformation of NBF-L triggered by NRT in the presence of NADH is through a series of tandem reaction which are irreversible in aqueous media. But in the synthesis of latent fluorescent probes NBF-L have some problems and discuss these problems.

參考文獻


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