Reactive 5'-substituted thymidine derivatives as potential inhibitors of nucleotide biosynthesis
作者:Robert D. Elliott、R. Wallace Brockman、John A. Montgomery
DOI:10.1021/jm00156a025
日期:1986.6
Fourteen derivatives of thymidine substituted at the 5'-position with haloacetamido (2-4), 2- and 3-bromopropionamido (5 and 6), bromoacetoxy (7), O-mesylglycolamido (8), bromo- and chloro-N-methylacetamido (10 and 11), bromomethanesulfonamido (12), ethyloxamido (13), 4- and 3-(fluorosulfonyl)benzamido (14 and 15), and (phenoxycarbonyl)amino (16) groups have been synthesized and evaluated as potential
胸腺嘧啶的十四个衍生物在5'-位被卤代乙酰氨基(2-4),2-和3-溴丙酰胺基(5和6),溴代乙酰氧基(7),O-甲磺酰基糖胺基(8),溴代和氯代N-取代已合成了甲基乙酰胺基(10和11),溴甲烷磺酰胺基(12),乙基草酰胺基(13),4-和3-(氟磺酰基)苯甲酰胺基(14和15)和(苯氧羰基)氨基(16)基团,并被评估为潜在的抑制剂代谢嘌呤和嘧啶核苷的酶。比较了这些核苷与巯基乙醇在pH 7下的反应速率,并与生物活性有关。化合物2、3和7对培养中的H.Ep.-2和L1210细胞具有细胞毒性,而5'-(溴和碘乙酰氨基)-5'-脱氧胸苷(2和3)对小鼠的P388白血病表现出良好的活性。