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    • 7. 发明申请
    • Compounds active in spinigosine 1-phosphate signaling
    • 在igigosine 1-磷酸信号传导中活跃的化合物
    • US20050222422A1
    • 2005-10-06
    • US10523337
    • 2003-07-30
    • Kevin LynchTimothy Macdonald
    • Kevin LynchTimothy Macdonald
    • C07D233/54C07F9/09C07F9/6506C07F9/28
    • C07F9/65068C07F9/091C07F9/094C07F9/6506
    • The present invention relates to S1P analogs that have activity as S1P receptor modulating agents and the use of such compounds to treat diseases associated with inappropriate S1P receptor activity. The compounds have the general structure of Formula (I) wherein R11 is C5-C18 alkyl or C5-C18 alkenyl; Q is selected from the group consisting of C3-C6 optionally substituted cycloalkyl, C3-C6 optionally substituted heterocyclic, C3-C6 optionally substituted aryl C3-C6 optionally substituted heteroaryl and —NH(CO)—; R2 is selected from the group consisting of H, C1-C4 alkyl, (C1-C4 alkyl)OH and (C1-C4 alkyl)NH2; R23 is H or C1-C4 alkyl, and R15 is selected from the group consisting of hydroxy, phosphonate, and of Formula (II) wherein X and R15 is selected from the group consisting of O and S; or a pharmaceutically acceptable salt or tautomer thereof.
    • 本发明涉及具有作为S1P受体调节剂的活性的S1P类似物以及这些化合物用于治疗与不适当S1P受体活性相关的疾病的用途。 这些化合物具有式(I)的通式结构,其中R 11是C 5 -C 18烷基或C 5 - C 1 -C 18链烯基; Q选自C 3 -C 6任选取代的环烷基,C 3 -C 6亚烷基,C 3 -C 6 - 任选取代的杂环,C 3 -C 6任选取代的芳基C 3 -C 6 -C 6任选取代的杂芳基和 - NH(CO) - ; R 2选自H,C 1 -C 4烷基,(C 1〜 C 4烷基)OH和(C 1 -C 4烷基)NH 2; R 23是H或C 1 -C 4烷基,R 15选自由以下组成的组: 羟基,膦酸酯和式(II)的化合物,其中X和R 15选自O和S; 或其药学上可接受的盐或互变异构体。