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

1,4-bis(ethyloxy)-6-fluoro-2,3-naphthalenedicarboxylic acid | 946838-76-2

中文名称
——
中文别名
——
英文名称
1,4-bis(ethyloxy)-6-fluoro-2,3-naphthalenedicarboxylic acid
英文别名
1,4-diethoxy-6-fluoronaphthalene-2,3-dicarboxylic acid
1,4-bis(ethyloxy)-6-fluoro-2,3-naphthalenedicarboxylic acid化学式
CAS
946838-76-2
化学式
C16H15FO6
mdl
——
分子量
322.29
InChiKey
UZJPXPDCLAQQGJ-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
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    93.1
  • 氢给体数:
    2
  • 氢受体数:
    7

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1,4-bis(ethyloxy)-6-fluoro-2,3-naphthalenedicarboxylic acid对氨基苯乙酸 、 Brine 、 magnesium sulfate甲醇 作用下, 以 N-甲基吡咯烷酮乙酸乙酯 为溶剂, 反应 0.17h, 以to give the title compound as a white solid (490 mg, 1.1 mmol)的产率得到{4-[4,9-bis(ethyloxy)-6-fluoro-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]phenyl}acetic acid
    参考文献:
    名称:
    Benzoisoindole derivatives and their use as EP4 receptor ligands
    摘要:
    一种式(I)的复合物或其药学上可接受的衍生物,其中R1至R8,X和Y如规范中所定义;制备这种化合物的方法;包括这种化合物的药物组成物;以及这种化合物在医学上的用途。
    公开号:
    US07718689B2
  • 作为产物:
    参考文献:
    名称:
    Discovery of {4-[4,9-bis(ethyloxy)-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-2-fluorophenyl}acetic acid (GSK726701A), a novel EP4 receptor partial agonist for the treatment of pain
    摘要:
    A novel series of EP4 agonists and antagonists have been identified, and then used to validate their potential in the treatment of inflammatory pain. This paper describes these novel ligands and their activity within a number of pre-chmcal models of pain, ultimately leading to the identification of the EP4 partial agonist GSK726701A. (C) 2018 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2018.03.091
点击查看最新优质反应信息

文献信息

  • Benzoisoindole Derivatives And Their Use As EP4 Receptor Ligands
    申请人:Healy Mark Patrick
    公开号:US20090030061A1
    公开(公告)日:2009-01-29
    A compound of formula (I) or a pharmaceutically acceptable derivative thereof, wherein R 1 to R 8 , X, and Y are as defined in the specification; a process for preparing such compounds; a pharmaceutical composition comprising such compounds; and the use of such compounds in medicine.
    一种式(I)的化合物或其药学上可接受的衍生物,其中R1至R8、X和Y如规范中所定义;制备这种化合物的过程;包含这种化合物的药物组合物;以及这种化合物在医学上的用途。
  • WO2007/93578
    申请人:——
    公开号:——
    公开(公告)日:——
  • US7718689B2
    申请人:——
    公开号:US7718689B2
    公开(公告)日:2010-05-18
  • Discovery of {4-[4,9-bis(ethyloxy)-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-2-fluorophenyl}acetic acid (GSK726701A), a novel EP4 receptor partial agonist for the treatment of pain
    作者:Mark P. Healy、Amanda C. Allan、Kristin Bailey、Andy Billinton、Iain P. Chessell、Nicholas M. Clayton、Gerard M.P. Giblin、Melanie A. Kay、Tarik Khaznadar、Anton D. Michel、Alan Naylor、Helen Price、David J. Spalding、David A. Stevens、Martin E. Swarbrick、Alexander W. Wilson
    DOI:10.1016/j.bmcl.2018.03.091
    日期:2018.6
    A novel series of EP4 agonists and antagonists have been identified, and then used to validate their potential in the treatment of inflammatory pain. This paper describes these novel ligands and their activity within a number of pre-chmcal models of pain, ultimately leading to the identification of the EP4 partial agonist GSK726701A. (C) 2018 Elsevier Ltd. All rights reserved.
  • Benzoisoindole derivatives and their use as EP4 receptor ligands
    申请人:Glaxo Group Limited
    公开号:US07718689B2
    公开(公告)日:2010-05-18
    A compound of formula (I) or a pharmaceutically acceptable derivative thereof, wherein R1 to R8, X, and Y are as defined in the specification; a process for preparing such compounds; a pharmaceutical composition comprising such compounds; and the use of such compounds in medicine.
    一种式(I)的复合物或其药学上可接受的衍生物,其中R1至R8,X和Y如规范中所定义;制备这种化合物的方法;包括这种化合物的药物组成物;以及这种化合物在医学上的用途。
查看更多