首页> 外文期刊>The Journal of Organic Chemistry >Photoinduced Fluorescent Cross-Linking of 5-Chloro- and 5-Fluoro-4-thiouridines with Thymidine
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Photoinduced Fluorescent Cross-Linking of 5-Chloro- and 5-Fluoro-4-thiouridines with Thymidine

机译:5-氯和5-氟-4-硫尿苷与胸苷的光诱导荧光交联

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摘要

Two highly fluorescent, thermally stable diastereomeric photoadducts, 3a,b, are formed when either 5-chloro-4-thiouridine, 1, or 5-fluoro-4-thiouridine, 2, are photoexcited with 366 nm UV light in the presence of thymidine (T). 5-Fluoro-4-thiouridine, 2, exhibits photoreactivity much higher than that of the 5-chloro derivative 1. In both cases the photoreaction is very clean, leading to highly eficient conversion of the 5-halogeno-4-thiouridine (1, 2) and T to photoadducts 3a,b. The identity and structure of 3a was confirmed using mass spectrometry and 2-D NMR. The epimeric relationship of 3a,b was established by UV circular dichroism spectroscopy. The geometry of the fluorescent photoadduct is consistent with formation of an interstrand cross-link in a DNA duplex if 1 or 2 is flanked by Tin an opposite strand.
机译:当将5氯-4-硫尿苷1或5氟-4-硫尿苷2在胸苷存在下用366 nm紫外光激发时,会形成两个高度荧光的,热稳定的非对映体光加合物3a,b。 (T)。 5-氟-4-硫尿苷2的光反应性比5-氯衍生物1高得多。在两种情况下,光反应都非常干净,导致5-卤代4-硫尿苷的高效转化(1, 2)和T为光加合物3a,b。使用质谱和2-D NMR确认3a的身份和结构。通过紫外圆二色谱法建立了3a,b的差向异构关系。如果1或2的两侧是锡的相反链,则荧光光加合物的几何形状与DNA双链体中链间交联的形成一致。

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