FTY720-derived anticancer agents
    6.
    发明授权
    FTY720-derived anticancer agents 有权
    FTY720衍生的抗癌剂

    公开(公告)号:US08309768B2

    公开(公告)日:2012-11-13

    申请号:US13305927

    申请日:2011-11-29

    摘要: A number of FTY720-derived compounds with antitumor activity are described. These compounds include the compounds of formula I: wherein R1 is independently selected from the group consisting of hydrogen, methyl. methoxy, and hydroxyl; R2 is independently selected from the group consisting of hydrogen, methoxy, and hydroxyl; R3 is independently selected from the group consisting of alkyl and cyclo-alkyl; and n is independently selected from 0 to 6. The compounds have lower immunosuppressive side effects as a result of not being phosphorylated by sphingosine kinase 2.

    摘要翻译: 描述了许多具有抗肿瘤活性的衍生自FTY720的化合物。 这些化合物包括式I化合物:其中R 1独立地选自氢,甲基。 甲氧基和羟基; R2独立地选自氢,甲氧基和羟基; R3独立地选自烷基和环烷基; 并且n独立地选自0至6.由于不被鞘氨醇激酶2磷酸化,所述化合物具有较低的免疫抑制副作用。

    FTY720-DERIVED ANTICANCER AGENTS
    7.
    发明申请
    FTY720-DERIVED ANTICANCER AGENTS 有权
    FTY720衍生的反应剂

    公开(公告)号:US20120136063A1

    公开(公告)日:2012-05-31

    申请号:US13305927

    申请日:2011-11-29

    摘要: A number of FTY720-derived compounds with antitumor activity are described. These compounds include the compounds of formula I: wherein R1 is independently selected from the group consisting of hydrogen, methyl. methoxy, and hydroxyl; R2 is independently selected from the group consisting of hydrogen, methoxy, and hydroxyl; R3 is independently selected from the group consisting of alkyl and cyclo-alkyl; and n is independently selected from 0 to 6. The compounds have lower immunosuppressive side effects as a result of not being phosphorylated by sphingosine kinase 2.

    摘要翻译: 描述了许多具有抗肿瘤活性的衍生自FTY720的化合物。 这些化合物包括式I化合物:其中R 1独立地选自氢,甲基。 甲氧基和羟基; R2独立地选自氢,甲氧基和羟基; R3独立地选自烷基和环烷基; 并且n独立地选自0至6.由于不被鞘氨醇激酶2磷酸化,所述化合物具有较低的免疫抑制副作用。