摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3,8-dimethoxy-5,11-dioxa-benzo[b]fluoren-10-one | 477594-12-0

中文名称
——
中文别名
——
英文名称
3,8-dimethoxy-5,11-dioxa-benzo[b]fluoren-10-one
英文别名
2,7-Dimethoxy-[1]benzofuro[3,2-b]chromen-11-one
3,8-dimethoxy-5,11-dioxa-benzo[b]fluoren-10-one化学式
CAS
477594-12-0
化学式
C17H12O5
mdl
——
分子量
296.279
InChiKey
QGTUXJXLWOTXMC-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):
    3.6
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    57.9
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    3,8-dimethoxy-5,11-dioxa-benzo[b]fluoren-10-one吡啶盐酸盐 作用下, 生成 3,8-Dihydroxy-5,11-dioxa-benzo[b]fluoren-10-one
    参考文献:
    名称:
    Constrained phytoestrogens and analogues as ERβ selective ligands
    摘要:
    A new series of ERbeta (ERbeta) selective ligands has been prepared. One of the compounds 6, structurally related to the phytoestrogen apigenin 4, displays a binding preference for ERbeta over ERalpha of over 40-fold. In addition to its binding selectivity, 6 was able to potently induce metallothionein (an ERbeta specific response in human SAOS-2 cells) while demonstrating low potency in an ERalpha dependant ERE-tk luciferase assay in MCF-7 cells. Such receptor and cell selectivity could make 6 a useful molecular probe for better understanding the role of ERbeta in mammalian physiology. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00394-9
  • 作为产物:
    描述:
    5-甲氧基水杨酸甲酯 、 2-Bromo-1-(2-fluoro-5-methoxyphenyl)ethanone 在 caesium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 3,8-dimethoxy-5,11-dioxa-benzo[b]fluoren-10-one
    参考文献:
    名称:
    Constrained phytoestrogens and analogues as ERβ selective ligands
    摘要:
    A new series of ERbeta (ERbeta) selective ligands has been prepared. One of the compounds 6, structurally related to the phytoestrogen apigenin 4, displays a binding preference for ERbeta over ERalpha of over 40-fold. In addition to its binding selectivity, 6 was able to potently induce metallothionein (an ERbeta specific response in human SAOS-2 cells) while demonstrating low potency in an ERalpha dependant ERE-tk luciferase assay in MCF-7 cells. Such receptor and cell selectivity could make 6 a useful molecular probe for better understanding the role of ERbeta in mammalian physiology. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00394-9
点击查看最新优质反应信息

文献信息

  • 5,11-dioxa-benzo[b]fluoren-10-one and 5-oxa-11-thia-benzo[b]fluoren-10-ones as estrogenic agents
    申请人:Wyeth
    公开号:US20020183310A1
    公开(公告)日:2002-12-05
    This invention provides estrogen receptor modulators of formula 1, having the structure 1 wherein X, Y 1 , Y 2 , Y 3 , Y 4 , Z 1 , Z 2 , Z 3 , and Z 4 are as defined in the specification, or a pharmaceutically acceptable salt thereof.
    该发明提供了公式1的雌激素受体调节剂,其结构为1,其中X,Y1,Y2,Y3,Y4,Z1,Z2,Z3和Z4如规范中所定义,或其药学上可接受的盐。
  • US6559177B2
    申请人:——
    公开号:US6559177B2
    公开(公告)日:2003-05-06
  • Constrained phytoestrogens and analogues as ERβ selective ligands
    作者:Chris P Miller、Michael D Collini、Heather A Harris
    DOI:10.1016/s0960-894x(03)00394-9
    日期:2003.7
    A new series of ERbeta (ERbeta) selective ligands has been prepared. One of the compounds 6, structurally related to the phytoestrogen apigenin 4, displays a binding preference for ERbeta over ERalpha of over 40-fold. In addition to its binding selectivity, 6 was able to potently induce metallothionein (an ERbeta specific response in human SAOS-2 cells) while demonstrating low potency in an ERalpha dependant ERE-tk luciferase assay in MCF-7 cells. Such receptor and cell selectivity could make 6 a useful molecular probe for better understanding the role of ERbeta in mammalian physiology. (C) 2003 Elsevier Science Ltd. All rights reserved.
查看更多