Inagaki K, Kidani Y
Bioinorg Chem. 1978 Aug;9(2):157-66. doi: 10.1016/s0006-3061(00)80287-2.
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(1) position by displacing a proton. When triammineplatinum was treated with 6-methyluracil or uridine in aqueous solution at pH7, 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(1) 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(1) position.
三氨合铂与尿嘧啶、6-甲基尿嘧啶或尿苷的配合物是在pH为7的水溶液中制备的。尿嘧啶与三氨合铂反应同时生成两种配合物。一种是三氨合铂从尿嘧啶中取代一个质子并配位到N(3)位的配合物,另一种是通过取代一个质子配位到N(1)位的配合物。当在pH为7的水溶液中用6-甲基尿嘧啶或尿苷处理三氨合铂时,仅得到配位到N(3)位的配合物。紫外(UV)、核磁共振(NMR)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信息。配位到尿嘧啶N(3)位的配合物的紫外和红外光谱行为与3-甲基尿嘧啶的非常相似。配位到尿嘧啶N(1)位的配合物的核磁共振谱显示出195Pt-质子的卫星峰,其耦合常数(39 Hz)为确定N(1)位的结合位点提供了有力证据。