Pentacyclic oxepines and derivatives thereof, compositions and methods
    20.
    发明授权
    Pentacyclic oxepines and derivatives thereof, compositions and methods 失效
    五环氧基及其衍生物,组合物和方法

    公开(公告)号:US07271264B2

    公开(公告)日:2007-09-18

    申请号:US10521998

    申请日:2003-07-18

    摘要: The present invention provides a compound of the formula (I) wherein R1 is —H, —OH, —O(C1-C4 alkyl), —OCOC6H5, —OCO(C1-C6 alkyl), or —OSO2(C2-C6 alkyl); R0, R2 and R3 are each independently —H, —OH, —O(C1-C4 alkyl), —OCOC6H5, —OCO(C1-C6 alkyl), —OSO2(C2-C6 alkyl) or halo; R4 is 1-piperidinyl, 1-pyrrolidinyl, methyl- 1-pyrrolidinyl, dimethyl-1-pyrrolidiny, 4-morpholino, dimethylamino, diethylamino, diisopropylamino, or 1-hexamethyleneimino; n is 2 or 3 X is —S— or —HC═CH—; G is —O—, —S—, —SO—, SO2, or —N(R5)—, wherein R5 is —H or C1-C4 alkyl; and Y is —O—, —S—, —NH—, —NMe—, or —CH2—; or a pharmaceutically acceptable salt thereof; pharmaceutical compositions thereof, optionally in combination with estrogen and progestin; methods of inhibiting a disease associated with estrogen deprivation; and methods for inhibiting a disease associated with an aberrant physiological response to endogenous estrogen.

    摘要翻译: 本发明提供式(I)的化合物,其中R 1是-H,-OH,-O(C 1 -C 4) 烷基),-OCOC 6 H 5,-OCO(C 1 -C 6烷基),或 (C 2 -C 6烷基);和(C 2 -C 6)烷基)。 R 0,R 2和R 3各自独立地为-H,-OH,-O(C 1 H 3) -C≡C4烷基),-OCOC 6 H 5,-OCO(C 1 -C 4烷基) 6烷基),-OSO 2(C 2 -C 6烷基)或卤素; R 4是1-哌啶基,1-吡咯烷基,甲基-1-吡咯烷基,二甲基-1-吡咯烷基,4-吗啉代,二甲基氨基,二乙基氨基,二异丙基氨基或1-六亚甲基亚氨基; n为2或3,X为-S-或-HC-CH-; G是-O - , - S-,-SO-,SO 2 - 或-N(R 5) - ,其中R 5, 是-H或C 1 -C 4烷基; 和Y是-O - , - S - , - NH-,-NMe - 或-CH 2 - 。 或其药学上可接受的盐; 其药物组合物,任选与雌激素和孕激素组合; 抑制与雌激素剥夺有关的疾病的方法; 以及用于抑制与内源性雌激素异常生理反应相关的疾病的方法。