SYNTHESIS OF CERTAIN 2′-DEOXYURIDINE DERIVATIVES CONTAINING SUBSTITUTED PHENOXY GROUPS ATTACHED TO C-5′; EVALUATION AS POTENTIAL dUTP ANALOGUES
作者:Jonathan H. Marriott、G. Wynne Aherne、Anthea Hardcastle、Michael Jarman
DOI:10.1081/ncn-100105905
日期:2001.9.30
Derivatives of 2′-deoxyuridine in which the 5′-OH group is replaced by a 2,3,6-trifluoro-5-hydroxy-4-nitrophenoxy or a 4-carboxy-2,3,6-trifluoro-5-hydroxyphenoxy group have been prepared for evaluation as possible dUTP analogues. They showed a weak ability to displace radiolabelled dUTP from a dUTP-binding antiserum. The corresponding compounds lacking the three fluorine substituents were prepared
2'-脱氧尿苷的衍生物,其中 5'-OH 基团被 2,3,6-三氟-5-羟基-4-硝基苯氧基或 4-羧基-2,3,6-三氟-5-羟基苯氧基取代小组已准备好评估可能的 dUTP 类似物。他们显示出从 dUTP 结合抗血清中置换放射性标记的 dUTP 的能力较弱。制备缺少三个氟取代基的相应化合物用于比较。