Synthesis of (E)-5-(3,3,3-trifluoro-1-propenyl)-2'-deoxyuridine and related analogs: potent and unusually selective antiviral activity of (E)-5-(3,3,3-trifluoro-1-propenyl)-2'-deoxyridine against herpes simplex virus type 1
作者:Donald E. Bergstrom、Jerry L. Ruth、P. Anantha Reddy、Erik De Clercq
DOI:10.1021/jm00369a009
日期:1984.3
Syntheses of (E)-5-(3,3,3-trifluoro-1-propenyl)-2'-deoxyuridine (TFPe-dUrd) (1), 5-(3,3,3-trifluoro-1-propyl)-2'-deoxyuridine (11), 5-(3,3,3-trifluoro-1-methoxy-1-propyl)-2'-deoxyuridine (8), and 5-(3,3,3-trifluoro-1-hydroxy-1-propyl)-2'-deoxyuridine (10) from 5-chloromercuri-2'-deoxyuridine are described. The antiviral activity of TFPe-dUrd was determined in cell culture against herpes simplex virus
(E)-5-(3,3,3-三氟-1-丙烯基)-2'-脱氧尿苷(TFPe-dUrd)(1),5-(3,3,3-三氟-1-丙基)的合成-2'-脱氧尿苷(11),5-(3,3,3-三氟-1-甲氧基-1-丙基)-2'-脱氧尿苷(8)和5-(3,3,3-三氟-1描述了来自5-氯巯基-2'-脱氧尿苷的-羟基-1-丙基)-2'-脱氧尿苷(10)。在细胞培养物中确定了TFPe-dUrd的抗病毒活性,针对1型单纯疱疹病毒(HSV-1),2型单纯疱疹病毒(HSV-2)和牛痘病毒,并与5-(1-丙烯基)- 2′-脱氧尿苷,5-(2-溴乙烯基)-2′-脱氧尿苷,5-碘-2′-脱氧尿苷和5-(三氟甲基)-2′-脱氧尿苷。TFPe-dUrd表现出对HSV-1的有效且非常规的选择性活性,病毒产量以0.03微克/ mL(0.09 microM)降低了2个对数;仅在290微克/ mL下L-1210细胞的生长被抑制了50%。