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3-(5-hydroxy-6,7-dimethoxy-4-oxo-4H-chromen-2-yl)phenyl N,N-dimethylcarbamate

中文名称
——
中文别名
——
英文名称
3-(5-hydroxy-6,7-dimethoxy-4-oxo-4H-chromen-2-yl)phenyl N,N-dimethylcarbamate
英文别名
[3-(5-hydroxy-6,7-dimethoxy-4-oxochromen-2-yl)phenyl] N,N-dimethylcarbamate
3-(5-hydroxy-6,7-dimethoxy-4-oxo-4H-chromen-2-yl)phenyl N,N-dimethylcarbamate化学式
CAS
——
化学式
C20H19NO7
mdl
——
分子量
385.373
InChiKey
AEMHSBVMLMRTLF-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):
    3.1
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    94.5
  • 氢给体数:
    1
  • 氢受体数:
    7

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

反应信息

  • 作为产物:
    描述:
    2,3,4-三甲氧基-6-羟基苯乙酮4-二甲氨基吡啶 、 aluminum (III) chloride 、 硫酸potassium carbonate 、 potassium iodide 、 potassium hydroxide 作用下, 以 乙醇二甲基亚砜乙腈 为溶剂, 反应 73.67h, 生成 3-(5-hydroxy-6,7-dimethoxy-4-oxo-4H-chromen-2-yl)phenyl N,N-dimethylcarbamate
    参考文献:
    名称:
    Multifunctional scutellarin–rivastigmine hybrids with cholinergic, antioxidant, biometal chelating and neuroprotective properties for the treatment of Alzheimer’s disease
    摘要:
    To discover multifunctional agents for the treatment of Alzheimer's disease (AD), a series of scutellarein carbamate derivatives were designed and synthesized based on the multitarget-directed ligand strategy. Their acetylcholinesterase and butyrylcholinesterase inhibitory activities, antioxidant activities, metal-chelating properties and neuroprotective effects against hydrogen peroxide induced PC12 cell injury were evaluated in vitro. The results showed that most of the synthetic compounds exhibited good multifunctional activities. In particular, compound 15c exhibited dual inhibitory potency on acetylcholinesterase and butyrylcholinesterase with IC50 values of 0.57 and 22.6 mu M, respectively, and good antioxidative activity, with a value 1.3-fold of Trolox. In addition, 15c acted as a selective biometal chelator and possessed neuroprotective effects. Furthermore, 15c could cross the blood-brain barrier (BBB) in vitro and had significant neuroprotective effects in scopolamine-induced cognitive impairment in mice. Taken together, these results suggest that compound 15c might be a potential multifunctional agent for the treatment of AD. (c) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2015.01.005
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文献信息

  • Multifunctional scutellarin–rivastigmine hybrids with cholinergic, antioxidant, biometal chelating and neuroprotective properties for the treatment of Alzheimer’s disease
    作者:Zhipei Sang、Yan Li、Xiaoming Qiang、Ganyuan Xiao、Qiang Liu、Zhenghuai Tan、Yong Deng
    DOI:10.1016/j.bmc.2015.01.005
    日期:2015.2
    To discover multifunctional agents for the treatment of Alzheimer's disease (AD), a series of scutellarein carbamate derivatives were designed and synthesized based on the multitarget-directed ligand strategy. Their acetylcholinesterase and butyrylcholinesterase inhibitory activities, antioxidant activities, metal-chelating properties and neuroprotective effects against hydrogen peroxide induced PC12 cell injury were evaluated in vitro. The results showed that most of the synthetic compounds exhibited good multifunctional activities. In particular, compound 15c exhibited dual inhibitory potency on acetylcholinesterase and butyrylcholinesterase with IC50 values of 0.57 and 22.6 mu M, respectively, and good antioxidative activity, with a value 1.3-fold of Trolox. In addition, 15c acted as a selective biometal chelator and possessed neuroprotective effects. Furthermore, 15c could cross the blood-brain barrier (BBB) in vitro and had significant neuroprotective effects in scopolamine-induced cognitive impairment in mice. Taken together, these results suggest that compound 15c might be a potential multifunctional agent for the treatment of AD. (c) 2015 Elsevier Ltd. All rights reserved.
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