Cyclic regimens using cyclocarbamate and cyclic amide derivatives
    10.
    发明授权
    Cyclic regimens using cyclocarbamate and cyclic amide derivatives 失效
    使用环状氨基甲酸酯和环状酰胺衍生物的循环方案

    公开(公告)号:US06380178B1

    公开(公告)日:2002-04-30

    申请号:US09552545

    申请日:2000-04-19

    IPC分类号: A61K3156

    摘要: This invention relates to cyclic combination therapies and regimens utilizing, in combination with progestins, substituted indoline derivative compounds which are antagonists of the progesterone receptor having the general structure: where A and B are independent substituents selected from S, CH or N; provided that when A is S, B is CH or N; and when B is S, A is CH or N; and A and B cannot both be CH; and when A and B both equal N, one N may be optionally substituted with an C1 to C6 alkyl group; R1 and R2 are independent substituents selected from the group of H, C1 to C6 alkyl, substituted C1 to C6 alkyl, C2 to C6 alkenyl, substituted C2 to C6 alkenyl, C2 to C6 alkynyl, substituted C2 to C6 alkynyl, C3 to C8 cycloalkyl, substituted C3 to C8 cycloalkyl, aryl, substituted aryl, heterocyclic, substituted heterocyclic, CORA, or NRBCORA; or R1 and R2 are fused to form optionally substituted 3 to 8 membered spirocyclic alkyl, alkenyl or heterocyclic ring, the heterocyclic ring containing one to three heteroatoms selected from the group of O, S and N; or pharmaceutically useful salts thereof. These methods of treatment may be used for contraception.

    摘要翻译: 本发明涉及利用与孕激素组合的取代二氢吲哚衍生物化合物的循环组合疗法和方案,所述二氢吲哚衍生化合物是具有以下通式结构的孕酮受体的拮抗剂:其中A和B是选自S,CH或N的独立取代基; 条件是当A为S时,B为CH或N; 当B为S时,A为CH或N; A和B不能同时为CH; 并且当A和B均等于N时,一个N可以任选地被C 1至C 6烷基取代; R1和R2是选自H,C1至C6烷基,取代C1至C6烷基,C2至C6烯基,取代C2至C6烯基,C2至C6炔基,取代C2至C6炔基,C3至C8环烷基的独立取代基 取代的C 3至C 8环烷基,芳基,取代的芳基,杂环,取代的杂环,CORA或NRBCORA; 或R 1和R 2稠合形成任选取代的3至8元螺环烷基,烯基或杂环,所述杂环含有一至三个选自O,S和N的杂原子; 或其药学上有用的盐。 这些治疗方法可用于避孕。