Synthesis and<i>in vitro</i>anti-human cytomegalovirus (hcmv) activity of certain alkenyl substituted cytosines and 5-halocytosines
作者:Arthur F. Lewis、Ganapathi R. Revankar、Robert F. Rando
DOI:10.1002/jhet.5570320517
日期:1995.9
The 1-[(Z)-2-penten-1-yl] and 1-(3-methyl-2-buten-1-yl) derivatives of cytosine, 5-bromocytosine, 5-fluorocytosine, and 5-iodocytosine were prepared by a reaction of the sodium salt of the requisite cytosine with (Z)-1-bromo-2-pentene and 4-bromo-2-methyl-2-butene, respectively. The eight alkenylcytosines 5a-5h were evaluated in cell culture for their anti-HCMV activity. Only the derivatives of 5-bromocytosine
制备了胞嘧啶,5-溴胞嘧啶,5-氟胞嘧啶和5-碘胞嘧啶的1-[((Z)-2-戊烯-1-基]和1-(3-甲基-2-丁烯-1-基)衍生物通过必需胞嘧啶的钠盐分别与(Z)-1-溴-2-戊烯和4-溴-2-甲基-2-丁烯反应。在细胞培养中评估了八个烯基胞嘧啶5a-5h的抗HCMV活性。在该测定中,仅5-溴胞嘧啶5c和5d的衍生物显示出轻微的活性。