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(α-bromo-benzyl)-phenyl-amine

中文名称
——
中文别名
——
英文名称
(α-bromo-benzyl)-phenyl-amine
英文别名
(α-Brom-benzyl)-phenyl-amin;(α-Brom-benzyl)-anilin;N-[bromo(phenyl)methyl]aniline
(α-bromo-benzyl)-phenyl-amine化学式
CAS
——
化学式
C13H12BrN
mdl
——
分子量
262.149
InChiKey
NNWNCGSNQHBDBN-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):
    4.3
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    12
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    (α-bromo-benzyl)-phenyl-amine 、 furan-2,3,5(4H)-trione pyridine (1:1) 生成 N-苄叉苯胺
    参考文献:
    名称:
    Adams; Vollweiler, Journal of the American Chemical Society, 1918, vol. 40, p. 1740
    摘要:
    DOI:
  • 作为产物:
    描述:
    α-Bromobenzyl benzoate 、 苯胺 生成 (α-bromo-benzyl)-phenyl-amine
    参考文献:
    名称:
    Adams; Vollweiler, Journal of the American Chemical Society, 1918, vol. 40, p. 1740
    摘要:
    DOI:
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文献信息

  • Lactams substituted by cyclic succinates as inhibitors of a beta protein production
    申请人:——
    公开号:US20020137737A1
    公开(公告)日:2002-09-26
    This invention relates to novel lactams having the Formula (I): 1 to their pharmaceutical compositions and to their methods of use. These novel compounds inhibit the processing of amyloid precursor protein and, more specifically, inhibit the production of A&bgr;-peptide, thereby acting to prevent the formation of neurological deposits of amyloid protein. More particularly, the present invention relates to the treatment of neurological disorders related to &bgr;-amyloid production such as Alzheimer's disease and Down's Syndrome.
    这项发明涉及具有式(I)的新型内内酰胺,以及它们的药物组合物和使用方法。这些新型化合物抑制淀粉样前体蛋白的加工,更具体地说,抑制Aβ-肽的产生,从而防止淀粉样蛋白的神经沉积形成。更具体地说,本发明涉及治疗与β-淀粉样蛋白产生相关的神经系统疾病,如阿尔茨海默病和唐氏综合征。
  • Lactams substituted by cyclic succinates as inhibitors of Abeta protein production
    申请人:Olson E. Richard
    公开号:US20050261274A1
    公开(公告)日:2005-11-24
    This invention relates to novel lactams having the Formula (I): to their pharmaceutical compositions and to their methods of use. These novel compounds inhibit the processing of amyloid precursor protein and, more specifically, inhibit the production of Aβ-peptide, thereby acting to prevent the formation of neurological deposits of amyloid protein. More particularly, the present invention relates to the treatment of neurological disorders related to β-amyloid production such as Alzheimer's disease and Down's Syndrome.
    本发明涉及具有公式(I)的新型内酰胺,其制药组成物和使用方法。这些新化合物抑制淀粉样前体蛋白的处理,更具体地抑制Aβ-肽的产生,从而防止神经元中淀粉样蛋白的沉积形成。更具体地,本发明涉及与β-淀粉样蛋白产生相关的神经系统疾病的治疗,如阿尔茨海默病和唐氏综合症。
  • Lactams substituted by cyclic succinates as inhibitors of A-beta protein production
    申请人:——
    公开号:US20030119815A1
    公开(公告)日:2003-06-26
    This invention relates to novel lactams having the Formula (I): 1 to their pharmaceutical compositions and to their methods of use. These novel compounds inhibit the processing of amyloid precursor protein and, more specifically, inhibit the production of A&bgr;-peptide, thereby acting to prevent the formation of neurological deposits of amyloid protein. More particularly, the present invention relates to the treatment of neurological disorders related to &bgr;-amyloid production such as Alzheimer's disease and Down's Syndrome.
    本发明涉及具有公式(I)的新型内酰胺,以及它们的制药组合物和使用方法。这些新化合物抑制淀粉样前体蛋白的处理,更具体地抑制Aβ-肽的产生,从而防止神经元中出现淀粉样蛋白质的沉积。更具体地说,本发明涉及治疗与β-淀粉样蛋白产生相关的神经系统疾病,如阿尔茨海默病和唐氏综合症。
  • LACTAMS SUBSTITUTED BY CYCLIC SUCCINATES AS INHIBITORS OF ABETTA PROTEIN PRODUCTION
    申请人:Olson E. Richard
    公开号:US20080103128A1
    公开(公告)日:2008-05-01
    This invention relates to novel lactams having the Formula (I): to their pharmaceutical compositions and to their methods of use. These novel compounds inhibit the processing of amyloid precursor protein and, more specifically, inhibit the production of Aβ-peptide, thereby acting to prevent the formation of neurological deposits of amyloid protein. More particularly, the present invention relates to the treatment of neurological disorders related to β-amyloid production such as Alzheimer's disease and Down's Syndrome.
    本发明涉及具有式(I)的新型内酰胺,它们的制药组合物和使用方法。这些新型化合物抑制淀粉样前体蛋白的加工,更具体地说,抑制Aβ肽的产生,从而防止神经沉积物的淀粉样蛋白形成。更具体地,本发明涉及与β-淀粉样蛋白产生相关的神经系统疾病的治疗,例如阿尔茨海默病和唐氏综合症。
  • LACTAMS SUBSTITUTED BY CYCLIC SUCCINATES AS INHIBITORS OF Abeta PROTEIN PRODUCTION
    申请人:Olson Richard E.
    公开号:US20090062256A1
    公开(公告)日:2009-03-05
    This invention relates to novel lactams having the Formula (I): to their pharmaceutical compositions and to their methods of use. These novel compounds inhibit the processing of amyloid precursor protein and, more specifically, inhibit the production of Aβ-peptide, thereby acting to prevent the formation of neurological deposits of amyloid protein. More particularly, the present invention relates to the treatment of neurological disorders related to β-amyloid production such as Alzheimer's disease and Down's Syndrome.
    本发明涉及具有公式(I)的新型内酰胺、它们的制药组合物以及它们的使用方法。这些新型化合物抑制淀粉样前体蛋白的处理,更具体地抑制Aβ-肽的产生,从而防止神经沉积物的淀粉样蛋白形成。更具体地,本发明涉及与β-淀粉样蛋白产生相关的神经系统疾病的治疗,例如阿尔茨海默病和唐氏综合症。
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