铂(II)和尿嘧啶衍生物之间的结合位点

Kenji Inagaki, Yoshinori Kidani
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引用次数: 13

摘要

在pH为7的水溶液中制备了尿嘧啶、6-甲基尿嘧啶和尿嘧啶的三胺铂配合物。尿嘧啶与三胺铂反应同时生成两个配合物。其中一种配合物是三胺铂取代尿嘧啶的一个质子并配位到N(3)位,另一种配合物通过取代一个质子而配位到N(1)位。在pH为7的水溶液中,用6-甲基尿嘧啶或尿嘧啶处理三胺铂时,只得到一个配位到N(3)的配合物。紫外(UV),核磁共振和红外(IR)光谱数据为确定这些配合物的结合位点提供了有用的信息。与尿嘧啶N(3)配位的配合物的紫外和红外光谱行为与3-甲基尿嘧啶非常相似。与尿嘧啶N(I)配位的配合物的核磁共振波谱显示195pt -质子的卫星峰,其偶联常数(39hz)为确定N(I)位置的结合位点提供了很好的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Binding sites between platinum(II) and uracil derivatives

The complexes of triammineplatinum with uracil, 6-methyluracil, or uridine were prepared in aqueous solution at pH 7. The reaction of uracil with triammineplatinum gave two complexes at the same time. One was a complex in which triammineplatinum displaced a proton from uracil and coordinated to the N(3) position, and the other the complex coordinated to the N(I) position by displacing a proton. When triammineplatinum was treated with 6-methyluracil or uridine in aqueous solution at pH 7, only a complex coordinated to the N(3) position was obtained. The ultraviolet (UV), NMR, and infrared (IR) spectral data provide useful information for determining the binding site of these complexes. The UV and IR spectral behaviors of the complex coordinated to the N(3) of uracil are very similar to those of 3-methyluracil. The NMR spectrum of the complex coordinated to the N(I) of uracil exhibits satellite peaks of 195Pt-proton and its coupling constant (39 Hz) gives good evidence for determining the binding site at the N(I) position.

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