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5-Fluoro-10-[4-(2-piperidin-1-ylethoxy)phenyl]-9-oxatetracyclo[9.8.0.02,7.012,17]nonadeca-1(11),2(7),3,5,12(17),13,15,18-octaen-15-ol

中文名称
——
中文别名
——
英文名称
5-Fluoro-10-[4-(2-piperidin-1-ylethoxy)phenyl]-9-oxatetracyclo[9.8.0.02,7.012,17]nonadeca-1(11),2(7),3,5,12(17),13,15,18-octaen-15-ol
英文别名
——
5-Fluoro-10-[4-(2-piperidin-1-ylethoxy)phenyl]-9-oxatetracyclo[9.8.0.02,7.012,17]nonadeca-1(11),2(7),3,5,12(17),13,15,18-octaen-15-ol化学式
CAS
——
化学式
C31H30FNO3
mdl
——
分子量
483.6
InChiKey
VPNPFKCNJXZCJJ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6.3
  • 重原子数:
    36
  • 可旋转键数:
    5
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    41.9
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • [EN] PENTACYCLIC OXEPINES AND DERIVATIVES THEREOF, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM<br/>[FR] OXEPINES PENTACYCLIQUES ET LEURS DERIVES, COMPOSITIONS ET METHODES ASSOCIEES
    申请人:LILLY CO ELI
    公开号:WO2004009578A2
    公开(公告)日:2004-01-29
    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-pyrrolidinyl, 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.
    本发明提供了化合物(I)的公式,其中R1为-H,-OH,-O(C1-C4烷基),-OCOC6H5,-OCO(C1-C6烷基)或-OSO2(C2-C6烷基);R0,R2和R3各自独立地为-H,-OH,-O(C1-C4烷基),-OCOC6H5,-OCO(C1-C6烷基),-OSO2(C2-C6烷基)或卤素;R4为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-吗啉基,二甲氨基,二乙氨基,二异丙基氨基或1-己亚甲基亚胺基;n为2或3,X为-S-或-HC = CH-;G为-O-,-S-,-SO-,SO2或-N(R5)-,其中R5为-H或C1-C4烷基;Y为-O-,-S-,-NH-,-NMe-或-CH2-;或其药学上可接受的盐;以及与雌激素和孕激素组合的药物组合物;用于抑制与雌激素缺乏有关的疾病的方法;以及用于抑制与内源性雌激素异常生理反应有关的疾病的方法。
  • Pentacyclic oxepines and derivatives thereof, compositions and methods
    申请人:Hinklin Jay Ronald
    公开号:US20050261277A1
    公开(公告)日:2005-11-24
    The present invention provides a compound of the formula (I) wherein R 1 is —H, —OH, —O(C 1 -C 4 alkyl), —OCOC —OCO(C 1 -C 6 alkyl), or —OSO 2 (C 2 -C 6 alkyl); R 0 , R 2 and R 3 are each independently —H, —OH, —O(C 1 -C 4 alkyl), —OCOC 6 H 5 , —OCO(C 1 -C 6 alkyl), —OSO 2 (C 2 -C 6 alkyl)or halo; R 4 is 1-piperidinyl, 1-pyrrolidinyl, methyl-1-pyrrolidinyl, dimethyl-1-pyrrolidinyl, 4-morpholino, dimethylamino, diethylamino, diisopropylamino, or 1-hexamethyleneimino; n is 2 or 3 X is —S— or —HC═H—; G is —O—, —S—, —SO—, SO 2 , or —N(R 5 )—, wherein R 5 is —H or C 1 -C 4 alkyl; and Y is —O—, —S—, —NH—, —NMe—, or —CH 2 —; 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.
    本发明提供了式(I)的化合物,其中R1为—H,—OH,—O(C1-C4烷基),—OCOC—OCO(C1-C6烷基)或—OSO2(C2-C6烷基); R0,R2和R3各自独立地为—H,—OH,—O(C1-C4烷基),—OCOC6H5,—OCO(C1-C6烷基),—OSO2(C2-C6烷基)或卤素; R4为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-吗啉基,二甲氨基,二乙氨基,二异丙基氨基或1-己亚甲基亚胺基; n为2或3,X为—S—或—HC═H—; G为—O—,—S—,—SO—,SO2或—N(R5)—,其中R5为—H或C1-C4烷基; Y为—O—,—S—,—NH—,—NMe—或—CH2—; 或其药学上可接受的盐; 其药物组合物,可选与雌激素和孕激素联合使用; 抑制与雌激素缺乏相关的疾病的方法; 以及抑制与内源性雌激素异常生理反应相关的疾病的方法。
  • PENTACYCLIC OXEPINES AND DERIVATIVES THEREOF, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
    申请人:ELI LILLY AND COMPANY
    公开号:EP1551822B1
    公开(公告)日:2006-12-20
  • US7271264B2
    申请人:——
    公开号:US7271264B2
    公开(公告)日:2007-09-18
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