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Synthesis of 5,10,15,20-Tetra4-(N-ethylpiperazinyl)phenyl-porphyrin and Its Interaction with DNA

机译:5,10,15,20-四4-(N-乙基哌嗪基)苯基-卟啉的合成及其与DNA的相互作用

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摘要

Piperazinyl-porphyrin, 5,10,15,20-tetra[4-(N-ethylpiperazinyl)phenyl]porphyrin (TEPPH2), was synthesized based on the special affinity of porphyrin to cancer cells and the antitumor activity of piperazine compounds. Its structure was characterized by UV-vis and 1H NMR spectra and elemental analysis. A model for the interaction between TEPPH2 and calf thymus DNA was built, and the binding mechanism was investigated by W-vis and fluorescence spectra. The results indicated that TEPPH2 could intercalate into the base pairs of DNA strongly. One calf thymus DNA molecule could bind 88 TEPPH2 molecules, and the binding constant K is 8.4×106 L-mol-1. The binding number and binding constant of TEPPH2 with DNA are higher than those of the known anti-tumor drugs,tetrakis(4-N-methylpyridyl)porphine and the Schiff bases Ca/sal-his and Ni/sal-aln.
机译:哌嗪基-卟啉5,10,15,20-四[4-(N-乙基哌嗪基)苯基]卟啉(TEPPH2)是基于卟啉对癌细胞的特殊亲和力和哌嗪化合物的抗肿瘤活性而合成的。通过紫外可见光谱和1H NMR光谱以及元素分析来表征其结构。建立了TEPPH2与小牛胸腺DNA相互作用的模型,并通过W-vis和荧光光谱研究了其结合机理。结果表明,TEPPH2可以强烈插入DNA的碱基对中。一个小胸腺DNA分子可以结合88个TEPPH2分子,结合常数K为8.4×106 L-mol-1。 TEPPH2与DNA的结合数和结合常数高于已知的抗肿瘤药物四(4-N-甲基吡啶基)卟啉和席夫碱Ca / sal-his和Ni / sal-aln。

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