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28 条记录 (耗时 0.039 秒)

    Pyrrolidine ester derivatives with oxytocin modulating activity
    5.
    发明授权
    Pyrrolidine ester derivatives with oxytocin modulating activity 有权
    吡咯烷酯衍生物与催产素调节活性

    公开(公告)号：US07189754B2

    公开(公告)日：2007-03-13

    申请号：US10471290

    申请日：2002-03-19

    申请人： Matthias Schwarz ,  Anna Quattropani ,  Alexander Scheer ,  Jerome Dorbais ,  Vincent Pomel

    发明人： Matthias Schwarz ,  Anna Quattropani ,  Alexander Scheer ,  Jerome Dorbais ,  Vincent Pomel

    IPC分类号： A61K31/40 ,  C07D207/00

    CPC分类号： C07D401/10 ,  A61K31/401 ,  C07D207/22 ,  C07D403/10

    摘要： The present invention is related to the use of pyrrolidine esters of formula (I) for the treatment and/or prevention of premature labor, premature birth and dysmenorrhea. In particular, the present invention is related to the use of pyrrolidine esters of formula (I) to modulate, notably to antagonize the oxytocin receptor. The present invention is furthermore related to novel pyrrolidine esters. X is selected from the group consisting of CR6R7, NOR6, NNR6R7; R is selected from the group comprising or consisting of C1–C6 alkyl, C2–C6 alkenyl, C2–C6 alkynyl, saturated or unsaturated 3–8-membered cycloalkyl which may contain 1 to 3 heteroatoms selected of N, O, S, aryl, heteroaryl, C1–C6-alkyl aryl, C1–C6-alkyl heteroaryl. R1 is selected from the group comprising or consisting of C1–C6-alkyl, C2–C6-alkenyl, C2–C6-alkynyl, aryl, heteroaryl, 3–8-membered cycloalkyl, acyl, C1–C6-alkyl aryl, C1–C6-alkyl heteroaryl, said cycloalkyl or aryl or heteroaryl groups may be fused with 1–2 further cycloalkyl or aryl or heteroaryl group

    摘要翻译： 本发明涉及式（I）的吡咯烷酯用于治疗和/或预防早产，早产和痛经的用途。 特别地，本发明涉及式（I）的吡咯烷酯的用途，特别是拮抗催产素受体。 本发明还涉及新的吡咯烷酯。 X选自CR 6，S 6，S 6，N 6，R 6，R 6， 7 ; R选自包含C 1 -C 6 -C 6烷基，C 2 -C 6 -C 6烷基，C 2 -C 6 - 烯基，C 2 -C 6炔基，饱和或不饱和的3-8元环烷基，其可以含有1-3个选自N，O，S，芳基，杂芳基的杂原子 C 1 -C 6 - 烷基芳基，C 1 -C 6 - 烷基杂芳基，C 1 -C 6 - 烷基芳基，C 1 -C 6 - R 1选自由C 1 -C 6 - C 6 - 烷基，C 2 - （C 1 -C 6）烷基组成的组或由C 1 -C 6 - C 6 - 烯基，C 2 -C 6 - 炔基，芳基，杂芳基，3-8元环烷基，酰基，C

    PHARMACEUTICALLY ACTIVE PYRROLIDINE ESTER DERIVATIVES
    7.
    发明申请
    PHARMACEUTICALLY ACTIVE PYRROLIDINE ESTER DERIVATIVES 审中-公开
    药用活性吡咯烷酮衍生物

    公开(公告)号：US20070129381A1

    公开(公告)日：2007-06-07

    申请号：US11620359

    申请日：2007-01-05

    申请人： Matthias Schwarz ,  Anna Quattropani ,  Alexander Scheer ,  Jerome Dorbais ,  Vincent Pomel

    发明人： Matthias Schwarz ,  Anna Quattropani ,  Alexander Scheer ,  Jerome Dorbais ,  Vincent Pomel

    IPC分类号： A61K31/506 ,  A61K31/4439 ,  A61K31/401 ,  C07D403/02

    CPC分类号： C07D401/10 ,  A61K31/401 ,  C07D207/22 ,  C07D403/10

    摘要： The present invention is related to the use of pyrrolidine esters of formula (I) for the treatment and/or prevention of premature labor, premature birth and dysmenorrhea. In particular, the present invention is related to the use of pyrrolidine esters of formula (I) to modulate, notably to antagonise the oxytocin receptor. The present invention is furthermore related to novel pyrrolidine esters. X is selected from the group consisting of CR6R7, NOR6, NNR6R7; R is selected from the group comprising or consisting of C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, saturated or unsaturated 3-8-membered cycloalkyl which may contain 1 to 3 heteroatoms selected of N, O, S, aryl, heteroaryl, C1-C6-alkyl aryl, C1-C6-alkyl heteroaryl. R1 is selected from the group comprising or consisting of C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, aryl, heteroaryl, 3-8-membered cycloalkyl, acyl, C1-C6-alkyl aryl, C1-C6-alkyl heteroaryl, said cycloalkyl or aryl or heteroaryl groups may be fused with 1-2 further cycloalkyl or aryl or heteroaryl group.

    摘要翻译： 本发明涉及式（I）的吡咯烷酯用于治疗和/或预防早产，早产和痛经的用途。 特别地，本发明涉及式（I）的吡咯烷酯的用途，特别是拮抗催产素受体。 本发明还涉及新的吡咯烷酯。 X选自CR 6，S 6，S 6，N 6，R 6，R 6， 7 ; R选自包含C 1 -C 6 -C 6烷基，C 2 -C 6 -C 6烷基，C 2 -C 6 - 烯基，C 2 -C 6炔基，饱和或不饱和的3-8元环烷基，其可以含有1-3个选自N，O，S，芳基，杂芳基的杂原子 C 1 -C 6 - 烷基芳基，C 1 -C 6 - 烷基杂芳基，C 1 -C 6 - 烷基芳基，C 1 -C 6 - R 1选自由C 1 -C 6 - C 6 - 烷基，C 2 - （C 1 -C 6）烷基组成的组或由C 1 -C 6 - C 6 - 烯基，C 2 -C 6 - 炔基，芳基，杂芳基，3-8元环烷基，酰基，C