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N-(1,3-Diphenyl-2-propyl)-hydroxylamin | 19293-68-6

中文名称
——
中文别名
——
英文名称
N-(1,3-Diphenyl-2-propyl)-hydroxylamin
英文别名
N-(1,3-diphenylpropan-2-yl)hydroxylamine
N-(1,3-Diphenyl-2-propyl)-hydroxylamin化学式
CAS
19293-68-6
化学式
C15H17NO
mdl
MFCD25259670
分子量
227.306
InChiKey
UXDHTFQFCLOKDV-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):
    3.4
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    32.3
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    参考文献:
    名称:
    1,2,4-Oxadiazolidin-3,5-diones and 1,3,5-triazin-2,4,6-triones as cytosolic phospholipase A2α inhibitors
    摘要:
    1,2,4-Oxadiazolidiin-3,5-dione and 1,3,5-triazin-2,4,6-trione scaffolds were employed as templates to incorporate the pharmacophore requirements of cytosolic phospholipase A(2)alpha Substrate mimetics. Inhibitors that are active in both enzyme, and cell-based assays were identified from both classes. From the SAR work carried out and modeling efforts around these templates, the triazinetrione scaffold with an additional substitution point was found to be more favorable. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.02.067
  • 作为产物:
    描述:
    二苄醚盐酸吡啶硼烷 作用下, 以 甲醇 为溶剂, 生成 N-(1,3-Diphenyl-2-propyl)-hydroxylamin
    参考文献:
    名称:
    1,2,4-Oxadiazolidin-3,5-diones and 1,3,5-triazin-2,4,6-triones as cytosolic phospholipase A2α inhibitors
    摘要:
    1,2,4-Oxadiazolidiin-3,5-dione and 1,3,5-triazin-2,4,6-trione scaffolds were employed as templates to incorporate the pharmacophore requirements of cytosolic phospholipase A(2)alpha Substrate mimetics. Inhibitors that are active in both enzyme, and cell-based assays were identified from both classes. From the SAR work carried out and modeling efforts around these templates, the triazinetrione scaffold with an additional substitution point was found to be more favorable. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.02.067
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文献信息

  • Reduction of oximes, oxime ethers, and oxime esters with diborane. Novel synthesis of amines
    作者:Henry Feuer、D. M. Braunstein
    DOI:10.1021/jo01258a062
    日期:1969.6
  • 1,2,4-Oxadiazolidin-3,5-diones and 1,3,5-triazin-2,4,6-triones as cytosolic phospholipase A2α inhibitors
    作者:Ariamala Gopalsamy、Hui Yang、John W. Ellingboe、John C. McKew、Steve Tam、Diane Joseph-McCarthy、Wen Zhang、Marina Shen、James D. Clark
    DOI:10.1016/j.bmcl.2006.02.067
    日期:2006.6
    1,2,4-Oxadiazolidiin-3,5-dione and 1,3,5-triazin-2,4,6-trione scaffolds were employed as templates to incorporate the pharmacophore requirements of cytosolic phospholipase A(2)alpha Substrate mimetics. Inhibitors that are active in both enzyme, and cell-based assays were identified from both classes. From the SAR work carried out and modeling efforts around these templates, the triazinetrione scaffold with an additional substitution point was found to be more favorable. (c) 2006 Elsevier Ltd. All rights reserved.
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