Hong C I, Mittelman A, Chheda G B
J Pharm Sci. 1978 Apr;67(4):569-71. doi: 10.1002/jps.2600670439.
Syntheses and biological activities of 12 N6-(n-alkylureido)purine ribonucleosides (alkyl chain length of 1--10, 16, and 18 carbons) and three N6-(n-alkylureido)purine ribonucleoside 5'-phosphates (chain length of 4, 9, and 10 carbons) are described. The N6-(n-alkylureido)purine ribonucleosides were prepared by a reaction of (2',3',5'-tri-O-acetyl-beta-D-ribofuranosyl)-9H-purine-6-carbamate and n-alkylamine in refluxing pyridine. The 5'-nucleotides were prepared by direct phosphorylation of the corresponding ribonucleoside with phosphorus oxychloride and triethyl phosphate. Some N6-(n-alkylureido)purine ribonucleosides (n-octyl, n-nonyl, and n-decyl) and their nucleotides showed a marked antiproliferative activity against L-1210 cells in culture.
描述了12种N6-(正烷基脲基)嘌呤核糖核苷(烷基链长度为1至10、16和18个碳)以及3种N6-(正烷基脲基)嘌呤核糖核苷5'-磷酸酯(链长度为4、9和10个碳)的合成及其生物活性。N6-(正烷基脲基)嘌呤核糖核苷是通过(2',3',5'-三-O-乙酰基-β-D-呋喃核糖基)-9H-嘌呤-6-氨基甲酸酯与正烷基胺在回流吡啶中反应制备的。5'-核苷酸是通过相应的核糖核苷与三氯氧磷和三乙磷酸直接磷酸化制备的。一些N6-(正烷基脲基)嘌呤核糖核苷(正辛基、正壬基和正癸基)及其核苷酸在培养中对L-1210细胞显示出显著的抗增殖活性。