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3-(4-dimethylaminophenethyloxyphenyl)pyrazole

中文名称
——
中文别名
——
英文名称
3-(4-dimethylaminophenethyloxyphenyl)pyrazole
英文别名
N,N-dimethyl-4-[2-[4-(1H-pyrazol-5-yl)phenoxy]ethyl]aniline
3-(4-dimethylaminophenethyloxyphenyl)pyrazole化学式
CAS
——
化学式
C19H21N3O
mdl
——
分子量
307.395
InChiKey
UKFZPMKSUZPUSD-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):
    3.9
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    41.2
  • 氢给体数:
    1
  • 氢受体数:
    3

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

  • 作为产物:
    描述:
    4-(二甲基氨基)苯乙醇4-(1H-吡唑-3-基)-苯酚三苯基膦偶氮二甲酸二乙酯 作用下, 以 四氢呋喃 为溶剂, 反应 16.0h, 以76%的产率得到3-(4-dimethylaminophenethyloxyphenyl)pyrazole
    参考文献:
    名称:
    Pyrazole derivatives as new potent and selective 20-hydroxy-5,8,11,14-eicosatetraenoic acid synthase inhibitors
    摘要:
    Improvement of the physical properties of pyrazole derivative 1, which we reported previously as a potent and selective 20-HETE synthase inhibitor (IC50 5.7nM), is described. Introduction of a sufficient substituted-amino group on the side chain enhanced the water-solubility of 1 (0.014mg/mL at pH6.8). Among the products, 2-piperazinoethoxy derivatives 3e and 6b showed solubility suitable for injection and potent inhibitory activity toward 20-HETE synthase (IC50 21.2 and 14.0 nM, respectively). (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2004.08.047
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文献信息

  • METHODS OF MODULATING CELL PROLIFERATION AND CYST FORMATION IN POLYCYSTIC KIDNEY AND LIVER DISEASES
    申请人:The Medical College of Wisconsin, Inc.
    公开号:EP2061450B1
    公开(公告)日:2017-04-19
  • Methods of modulating cell proliferation and cyst formation in polycystic kidney and liver diseases
    申请人:Sweeney William E.
    公开号:US20080167382A1
    公开(公告)日:2008-07-10
    The present invention provides a method for preferentially reducing the proliferation of cystic epithelial cells in the kidney or bile duct in a mammal in need thereof by administering a 20-HETE synthesizing enzyme inhibitor or a 20-HETE antagonist to the mammal in an amount sufficient to preferentially reduce the proliferation of cystic epithelial cells over normal epithelial cells such as tubule epithelial cells in the kidney or bile duct. The present invention also provides a method for preventing or treating autosomal dominant polycystic kidney disease (ADPKD), autosomal recessive polycystic kidney disease (ARPKD), ARPKD associated congenital hepatic fibrosis, ARPKD associated Caroli's disease, or cholangiocarcinoma in a mammal in need thereof by administering a 20-HETE synthesizing enzyme inhibitor or a 20-HETE antagonist to the mammal in an amount sufficient to prevent or treat the disease.
  • Methods of Modulating Cell Proliferation and Cyst Formation in Polycystic Kidney and Liver Diseases
    申请人:Sweeney William E.
    公开号:US20140329811A1
    公开(公告)日:2014-11-06
    The present invention provides a method for preferentially reducing the proliferation of cystic epithelial cells in the kidney or bile duct in a mammal in need thereof by administering a 20-HETE synthesizing enzyme inhibitor or a 20-HETE antagonist to the mammal in an amount sufficient to preferentially reduce the proliferation of cystic epithelial cells over normal epithelial cells such as tubule epithelial cells in the kidney or bile duct. The present invention also provides a method for preventing or treating autosomal dominant polycystic kidney disease (ADPKD), autosomal recessive polycystic kidney disease (ARPKD), ARPKD associated congenital hepatic fibrosis, ARPKD associated Caroli's disease, or cholangiocarcinoma in a mammal in need thereof by administering a 20-HETE synthesizing enzyme inhibitor or a 20-HETE antagonist to the mammal in an amount sufficient to prevent or treat the disease.
  • US8846764B2
    申请人:——
    公开号:US8846764B2
    公开(公告)日:2014-09-30
  • US9511072B2
    申请人:——
    公开号:US9511072B2
    公开(公告)日:2016-12-06
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