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FT-ICR study of novel organometallic compounds as potential anticarcinogenics: Interaction with nucleobases

机译:新型有机金属化合物的FT-ICR研究作为潜在的防毒性:与核碱基的相互作用

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DPYR is one of the most important anionic-fragments detected. All the nucleobases can substitute one of the methyl groups of CS1, while only purines can do the same with one of the phenyl groups of CS2. No substitution of cyclohexyl groups in CS3 has been detected. All the nucleobases can substitute the DPYR group of CS3 (cationic mode) and CS2 (anionic mode), while only cytosine can react with CS1 (it was found a specific interaction between trymethyl thin and cytosine).
机译:DPYR是检测到最重要的阴离子片段之一。所有核碱基都可以替代CS1的甲基之一,而仅嘌呤可以与CS2的苯基之一相同。未检测到CS3中的环己基的替代。所有核碱基都可以替代CS3(阳离子模式)和CS2(阴离子模式)的DPYR基团,而只有胞嘧啶可以与CS1反应(发现试验甲基薄和胞嘧啶之间的特异性相互作用)。

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