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N-(3,4-dihydro-2H-benzo[b][1,4]dioxepin-7-yl)-6-(2,5-dimethyl-phenyl)-nicotinamide | 717113-87-6

中文名称
——
中文别名
——
英文名称
N-(3,4-dihydro-2H-benzo[b][1,4]dioxepin-7-yl)-6-(2,5-dimethyl-phenyl)-nicotinamide
英文别名
N-(3,4-dihydro-2H-1,5-benzodioxepin-7-yl)-6-(2,5-dimethylphenyl)pyridine-3-carboxamide
N-(3,4-dihydro-2H-benzo[b][1,4]dioxepin-7-yl)-6-(2,5-dimethyl-phenyl)-nicotinamide化学式
CAS
717113-87-6
化学式
C23H22N2O3
mdl
——
分子量
374.439
InChiKey
LREGCMPJCJCVPK-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):
    4.2
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    60.4
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • Substituted biphenyl-4-carboxylic acid arylamide analogues
    申请人:Bakthavatchalam Rajagopal
    公开号:US20060100245A1
    公开(公告)日:2006-05-11
    Substituted biphenyl-4-carboxylic acid arylamide analogues capable of modulating receptor activity, are provided. Such ligands may be used to modulate receptor activity in vivo or in vitro, and are particularly useful in the treatment of pain and other conditions associated with receptor activation in humans, domesticated companion animals and livestock animals. Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for receptor localization studies.
    提供了能够调节受体活性的取代联苯-4-羧酸芳香酰胺类似物。这样的配体可以用于体内或体外调节受体活性,并且在治疗与人类、家畜伴侣动物和家畜动物中的受体激活有关的疼痛和其他疾病方面特别有用。提供了用于治疗此类疾病的制药组合物和方法,以及用于受体定位研究的配体使用方法。
  • SUBSTITUTED BIARYL-4-CARBOXYLIC ACID ARYLAMIDE ANALOGUES AS CAPSAICIN RECEPTOR MODULATORS
    申请人:NEUROGEN CORPORATION
    公开号:EP1575918A2
    公开(公告)日:2005-09-21
  • [EN] SUBSTITUTED BIPHENYL-4-CARBOXYLIC ACID ARYLAMIDE ANALOGUES<br/>[FR] ANALOGUES D'ARYLAMIDE D'ACIDE BIPHENYL-4-CARBOXYLIQUE SUBSTITUES
    申请人:NEUROGEN CORP
    公开号:WO2004056774A2
    公开(公告)日:2004-07-08
    Substituted biphenyl-4-carboxylic acid arylamide analogues of the formula (I) capable of modulating receptor activity, are provided. Such ligands may be used to modulate receptor activity in vivo or in vitro, and are particularly useful in the treatment of pain and other conditions associated with receptor activation in humans, domesticated companion animals and livestock animals. Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for receptor localization studies.
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