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(E)-3-[4-(oxiran-2-ylmethoxy)phenyl]-1-phenylprop-2-en-1-one

中文名称
——
中文别名
——
英文名称
(E)-3-[4-(oxiran-2-ylmethoxy)phenyl]-1-phenylprop-2-en-1-one
英文别名
——
(E)-3-[4-(oxiran-2-ylmethoxy)phenyl]-1-phenylprop-2-en-1-one化学式
CAS
——
化学式
C18H16O3
mdl
——
分子量
280.323
InChiKey
PQPTYTNIRCXCAV-DHZHZOJOSA-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:
    21
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    38.8
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    哌啶(E)-3-[4-(oxiran-2-ylmethoxy)phenyl]-1-phenylprop-2-en-1-one甲醇 为溶剂, 反应 6.0h, 生成 (E)-3-[4-(2-hydroxy-3-piperidin-1-ylpropoxy)phenyl]-1-phenylprop-2-en-1-one
    参考文献:
    名称:
    Chalcone based aryloxypropanolamines as potential antihyperglycemic agents
    摘要:
    A series of chalcone based aryloxypropanolamines were synthesized and evaluated for their antihyperglycemic activity in SLM and STZ rat models. Most of the compounds exhibited moderate to good activity ranging from 6.5% to 31.1% in SLM and 8.3% to 22.6% in STZ models, respectively. The most potent compound 5g exhibited glucose lowering of 26.7% in SLM and 22.6% in STZ models. A definite structure-activity relationship was observed while varying the nature as well as the position of the amine in ring B. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.10.068
  • 作为产物:
    描述:
    苯乙酮sodium hydroxide 、 sodium hydride 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 反应 10.0h, 生成 (E)-3-[4-(oxiran-2-ylmethoxy)phenyl]-1-phenylprop-2-en-1-one
    参考文献:
    名称:
    Chalcone based aryloxypropanolamines as potential antihyperglycemic agents
    摘要:
    A series of chalcone based aryloxypropanolamines were synthesized and evaluated for their antihyperglycemic activity in SLM and STZ rat models. Most of the compounds exhibited moderate to good activity ranging from 6.5% to 31.1% in SLM and 8.3% to 22.6% in STZ models, respectively. The most potent compound 5g exhibited glucose lowering of 26.7% in SLM and 22.6% in STZ models. A definite structure-activity relationship was observed while varying the nature as well as the position of the amine in ring B. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2006.10.068
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文献信息

  • Chalcone based aryloxypropanolamines as potential antihyperglycemic agents
    作者:Poonam Shukla、Amar Bahadur Singh、Arvind Kumar Srivastava、Ram Pratap
    DOI:10.1016/j.bmcl.2006.10.068
    日期:2007.2
    A series of chalcone based aryloxypropanolamines were synthesized and evaluated for their antihyperglycemic activity in SLM and STZ rat models. Most of the compounds exhibited moderate to good activity ranging from 6.5% to 31.1% in SLM and 8.3% to 22.6% in STZ models, respectively. The most potent compound 5g exhibited glucose lowering of 26.7% in SLM and 22.6% in STZ models. A definite structure-activity relationship was observed while varying the nature as well as the position of the amine in ring B. (c) 2006 Elsevier Ltd. All rights reserved.
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