Arenavirus growth inhibitor comprising polycyclic carbamoyl pyridone derivative

    公开(公告)号:US12098151B2

    公开(公告)日:2024-09-24

    申请号:US17957103

    申请日:2022-09-30

    摘要: The present invention provides a compound having antiviral activity, especially having arenavirus proliferation inhibitory activity, and/or a medicament comprising the compound. More preferably, the present invention provides a compound having proliferation inhibitory activity on the Old World arenaviruses such as Luna virus, Lassa virus, and lymphocytic choriomeningitis virus and/or the New World arenaviruses such as Junin virus, and/or a medicament comprising the compound.
    An arenavirus proliferation inhibitor comprising a compound represented by Formula (I) or a prodrug thereof or a pharmaceutically acceptable salt thereof:




    (wherein R1 is carboxy, or the like: A3 is CR2 or N; R2 is a hydrogen atom, halogen, hydroxy, or the like; R3 is a hydrogen atom, hydroxy, carboxy, cyano, formyl, alkyl optionally substituted with Substituent group F, or the like; either A1 or A2 is CR5R6, and the other is NR7, or A1 is CR8R9, and A2 is CR10OR11; and R5, R6, R7, R8, R9, R10, and R11 are each independently a hydrogen atom, carboxy, cyano, alkyl optionally substituted with Substituent group F, or the like).

    PHARMACEUTICAL COMPOSITION FOR TREATING FATTY LIVER DISEASE

    公开(公告)号:US20230210822A1

    公开(公告)日:2023-07-06

    申请号:US17926273

    申请日:2021-05-20

    IPC分类号: A61K31/4184 A61P1/16

    CPC分类号: A61K31/4184 A61P1/16

    摘要: Provided is a pharmaceutical composition for treating and/or preventing fatty liver disease, particularly nonalcoholic fatty liver disease, the pharmaceutical composition having an excellent ACC2-selective inhibitory action and having no side effects such as an increase in plasma triglyceride or a decrease in platelet concentration.
    A pharmaceutical composition for treating and/or preventing fatty liver disease, the pharmaceutical composition comprising a compound represented by Formula (I):






    wherein
    R1 is haloalkyl or non-aromatic carbocyclyl,
    R2 is a hydrogen atom or halogen,
    R3 is halogen,
    ring A is a group represented by the formula:










    -L1- is —O—(CH2)—, —(CH2)2—, or the like,
    R4 is alkyl or haloalkyl, and
    R5 is alkylcarbonyl or carbamoyl,


    or a pharmaceutically acceptable salt thereof.