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[2-(4-Bromophenyl)ethyl]urea | 158893-30-2

中文名称
——
中文别名
——
英文名称
[2-(4-Bromophenyl)ethyl]urea
英文别名
2-(4-bromophenyl)ethylurea
[2-(4-Bromophenyl)ethyl]urea化学式
CAS
158893-30-2
化学式
C9H11BrN2O
mdl
——
分子量
243.103
InChiKey
GGWVITFHXANSNX-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):
    1.6
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    55.1
  • 氢给体数:
    2
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    [2-(4-Bromophenyl)ethyl]urea氢氧化钾 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 11.0h, 生成 ethyl 1-(2-(4-bromophenyl)ethyl)-2,4,5-trioxoimidazolidine-3-acetate
    参考文献:
    名称:
    Highly Selective Aldose Reductase Inhibitors. 1. 3-(Arylalkyl)-2,4,5-trioxoimidazolidine-1-acetic Acids
    摘要:
    A series of 3-(arylalkyl)-2,4,5-trioxoimidazolidine-1-acids (1) was prepared and tested for aldose reductase (AR) and aldehyde reductase (ALR) inhibitory activities. These compounds showed strong inhibitory activity against AR without significant inhibitory activity for ALR. The ratio of IC50(ALR)/IC50(AR) was > 1000 in some compouds. On the basis of pharmacological tests such as the recovery of reduced motor nerve conduction velocity and toxicological profile, 3-(3-nitrobenzyl)-2,4,5-trioxoimidazolidine-1-acid (NZ-314) was selected as the candidate for clinical development.
    DOI:
    10.1021/jm9508393
  • 作为产物:
    描述:
    2-(4-溴苯)乙胺盐酸盐尿素盐酸 作用下, 以 为溶剂, 反应 3.0h, 生成 [2-(4-Bromophenyl)ethyl]urea
    参考文献:
    名称:
    Highly Selective Aldose Reductase Inhibitors. 1. 3-(Arylalkyl)-2,4,5-trioxoimidazolidine-1-acetic Acids
    摘要:
    A series of 3-(arylalkyl)-2,4,5-trioxoimidazolidine-1-acids (1) was prepared and tested for aldose reductase (AR) and aldehyde reductase (ALR) inhibitory activities. These compounds showed strong inhibitory activity against AR without significant inhibitory activity for ALR. The ratio of IC50(ALR)/IC50(AR) was > 1000 in some compouds. On the basis of pharmacological tests such as the recovery of reduced motor nerve conduction velocity and toxicological profile, 3-(3-nitrobenzyl)-2,4,5-trioxoimidazolidine-1-acid (NZ-314) was selected as the candidate for clinical development.
    DOI:
    10.1021/jm9508393
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文献信息

  • [EN] NOVEL THIOPHENE AMIDINES, COMPOSITIONS THEREOF, AND METHODS OF TREATING COMPLEMENT-MEDIATED DISEASES AND CONDITIONS<br/>[FR] NOUVELLES AMIDINES DE THIOPHENE, COMPOSITIONS DE CES AMIDINES ET PROCEDE POUR TRAITER DES MALADIES ET DES ETATS MEDIES PAR LE COMPLEMENT
    申请人:DIMENSIONAL PHARM INC
    公开号:WO2003099805A1
    公开(公告)日:2003-12-04
    Disclosed is a method for treating the symptoms of an acute or chronic disorder mediated by the classical pathway of the complement cascade, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula (I) or a solvate, hydrate or pharmaceutically acceptable salt thereof; wherein R1, R2, R3, R4 and R7 are defined in the specification, Z is SO or SO2, and Ar is an aromatic or heteroaromatic group as defined herein.
    揭示了一种治疗急性或慢性疾病症状的方法,该方法通过补体级联的经典途径介导,包括向需要此类治疗的哺乳动物施用化合物I的治疗有效量或其溶剂化合物、水合物或药用可接受盐;其中规范中定义了R1、R2、R3、R4和R7,Z为SO或SO2,Ar为本规范中定义的芳香族或杂环芳基。
  • Novel thiophene amidines, compositions thereof, and methods of treating complement-mediated diseases and conditions
    申请人:3-Dimensional Pharmaceuticals, Inc.
    公开号:US20040009995A1
    公开(公告)日:2004-01-15
    Disclosed is a method for treating the symptoms of an acute or chronic disorder mediated by the classical pathway of the complement cascade, comprising administering to a mammal in need of such treatment a therapeutically effective amount of a compound of Formula I 1 or a solvate, hydrate or pharmaceutically acceptable salt thereof; wherein R 1 , R 2 , R 3 , R 4 and R 7 are defined in the specification, Z is SO or SO 2 , and Ar is an aromatic or heteroaromatic group as defined herein.
    揭示了一种治疗急性或慢性疾病症状的方法,该方法通过补体级联的经典途径介导,包括向需要此类治疗的哺乳动物施用公式I的化合物的治疗有效量或其溶剂化合物、水合物或药用可接受盐;其中在规范中定义了R1、R2、R3、R4和R7,Z为SO或SO2,Ar为本文中定义的芳香族或杂环芳基。
  • UREA BASED LIPOXYGENASE INHIBITING COMPOUNDS
    申请人:ABBOTT LABORATORIES
    公开号:EP0588785A1
    公开(公告)日:1994-03-30
  • EP0588785A4
    申请人:——
    公开号:EP0588785A4
    公开(公告)日:1991-12-30
  • NOVEL THIOPHENE AMIDINES, COMPOSITIONS THEREOF, AND METHODS OF TREATING COMPLEMENT-MEDIATED DISEASES AND CONDITIONS
    申请人:3-DIMENSIONAL PHARMACEUTICALS, INC.
    公开号:EP1549632A1
    公开(公告)日:2005-07-06
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