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[(S)-1-(4-bromo-phenyl)-ethyl]-(3-oxo-3-phenyl-propyl)-carbamic acid methyl ester | 1114563-47-1

中文名称
——
中文别名
——
英文名称
[(S)-1-(4-bromo-phenyl)-ethyl]-(3-oxo-3-phenyl-propyl)-carbamic acid methyl ester
英文别名
methyl N-[(1S)-1-(4-bromophenyl)ethyl]-N-(3-oxo-3-phenylpropyl)carbamate
[(S)-1-(4-bromo-phenyl)-ethyl]-(3-oxo-3-phenyl-propyl)-carbamic acid methyl ester化学式
CAS
1114563-47-1
化学式
C19H20BrNO3
mdl
——
分子量
390.277
InChiKey
LHYYZVPEAPXBPW-AWEZNQCLSA-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
  • 重原子数:
    24
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    46.6
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • [EN] CYCLIC INHIBITORS OF 11ß-HYDROXYSTERIOD DEHYDROGENASE 1<br/>[FR] INHIBITEURS CYCLIQUES DE LA 11?-HYDROXYSTÉROÏDE DÉSHYDROGÉNASE 1
    申请人:VITAE PHARMACEUTICALS INC
    公开号:WO2009017664A1
    公开(公告)日:2009-02-05
    This invention relates to novel compounds of the Formula (I), (Ia), (Ib), (Ic), (Id), (Ie), (If), (Ig), (Ih); (Ii); (Ij), (Ik), (II) pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful for the therapeutic treatment of diseases associated with the modulation or inhibition of 11 β-HSD1 in mammals. The invention further relates to pharmaceutical compositions of the novel compounds and methods for their use in the reduction or control of the production of cortisol in a cell or the inhibition of the conversion of cortisone to cortisol in a cell.
    本发明涉及式(I)、(Ia)、(Ib)、(Ic)、(Id)、(Ie)、(If)、(Ig)、(Ih);(Ii);(Ij),(Ik),(II)的新颖化合物,其药用可接受的盐以及药物组合物,这些化合物对于治疗与调节或抑制哺乳动物中的11β-HSD1相关的疾病是有用的。本发明进一步涉及新颖化合物的药物组合物及其在减少或控制细胞中皮质醇的产生或抑制细胞中将可的松转化为皮质醇的方法。
  • INHIBITORS OF 11beta-HYDROXYSTEROID DEHYDROGENASE 1
    申请人:Himmelsbach Frank
    公开号:US20120108578A1
    公开(公告)日:2012-05-03
    This invention relates to novel compounds of the Formula (I), (Ia 1-10 ), (Ib 1-10 ), (Ic 1-10 ), (Id 1-7 ), (Ie 1-5 ) pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful for the therapeutic treatment of diseases associated with the modulation or inhibition of 11β-HSD1 in mammals. The invention further relates to pharmaceutical compositions of the novel compounds and methods for their use in the reduction or control of the production of cortisol in a cell or the inhibition of the conversion of cortisone to cortisol in a cell.
    这项发明涉及公式(I)、(Ia1-10)、(Ib1-10)、(Ic1-10)、(Id1-7)、(Ie1-5)的新化合物,其药学上可接受的盐,以及其药物组合物,这些化合物对于治疗与哺乳动物中11β-HSD1的调节或抑制相关的疾病是有用的。该发明还涉及这些新化合物的药物组合物和它们在细胞中减少或控制皮质醇的产生或抑制皮质醇酮转化为皮质醇的方法的用途。
  • CYCLIC INHIBITORS OF 11beta-HYDROXYSTEROID DEHYDROGENASE 1
    申请人:Eckhardt Matthias
    公开号:US20110312950A1
    公开(公告)日:2011-12-22
    This invention relates to novel compounds of the Formula Formulas (I), (Ia 1-20 ), (Ib 1-20 ), (Ic 1-20 ), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful for the therapeutic treatment of diseases associated with the modulation or inhibition of 11β-HSD1 in mammals. The invention further relates to pharmaceutical compositions of the novel compounds and methods for their use in the reduction or control of the production of cortisol in a cell or the inhibition of the conversion of cortisone to cortisol in a cell.
    本发明涉及公式(I),(Ia1-20),(Ib1-20),(Ic1-20)的新化合物,其药学上可接受的盐和药物组合物,用于治疗与哺乳动物中11β-HSD1调节或抑制相关的疾病。本发明还涉及新化合物的药物组合物和其在细胞中减少或控制皮质醇的产生或抑制皮质酮转化为皮质醇的方法。
  • CYCLIC INHIBITORS OF 11BETA-HYDROXYSTEROID DEHYDROGENASE 1
    申请人:Claremon David A.
    公开号:US20110015157A1
    公开(公告)日:2011-01-20
    This invention relates to novel compounds of the Formula (I), (Ia), (Ib), (Ic), (Id), (Ie), (If), (Ig), (Ih); (Ii); (Ij), (Ik), (II) pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful for the therapeutic treatment of diseases associated with the modulation or inhibition of 11 β-HSD1 in mammals. The invention further relates to pharmaceutical compositions of the novel compounds and methods for their use in the reduction or control of the production of cortisol in a cell or the inhibition of the conversion of cortisone to cortisol in a cell.
    本发明涉及式(I)、(Ia)、(Ib)、(Ic)、(Id)、(Ie)、(If)、(Ig)、(Ih)、(Ii)、(Ij)、(Ik)、(II)的新化合物,以及其药学上可接受的盐和制药组合物,用于治疗与哺乳动物11β-HSD1调节或抑制相关的疾病。本发明还涉及新化合物的制药组合物以及其在细胞中减少或控制皮质醇的产生或抑制皮质酮转化为皮质醇的方法。
  • CYCLIC INHIBITORS OF 11ß -HYDROXYSTERIOD DEHYDROGENASE 1
    申请人:Vitae Pharmaceuticals, Inc.
    公开号:EP2183228B1
    公开(公告)日:2014-08-20
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