Synthesis of Sulfated Cerebroside Analogs Having Mimicks of Ceramide and Their Anti-human Immunodeficiency Virus Type 1 Activities.
作者:Hiroyuki YOSHIDA、Kiyoshi IKEDA、Kazuo ACHIWA、Hiroo HOSINO
DOI:10.1248/cpb.43.594
日期:——
Various sulfated cerebroside analogs, which are mimicks of cerebroside, have been prepared from per-O-acetylated D-glucose, per-O-acetylated D-galactose, and per-O-acetylated D-lactose with ethyleneglycol dodecyl ether, 3-docosyloxy-1-propanol, 2-hydroxymethyl-1, 3-O-dimyristyl-1, 3-propanediol, and L-serine diamide derivatives as ceramide moieties. The synthesized sulfated glycolipids showed anti-HIV-1 activities.
以过-O-乙酰化 D-葡萄糖、过-O-乙酰化 D-半乳糖和过-O-乙酰化 D-乳糖为神经酰胺分子,以乙二醇十二烷基醚、3-二十二烷氧基-1-丙醇、2-羟甲基-1,3-O-二肉豆蔻基-1,3-丙二醇和 L-丝氨酸二酰胺衍生物为神经酰胺分子,制备了各种硫酸化脑苷脂类似物,它们是脑苷脂的模拟物。合成的硫酸化糖脂具有抗 HIV-1 活性。