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N,N-diethyl-2-selenonaphthylamide

中文名称
——
中文别名
——
英文名称
N,N-diethyl-2-selenonaphthylamide
英文别名
N,N-diethylnaphthalene-2-carboselenoamide
N,N-diethyl-2-selenonaphthylamide化学式
CAS
——
化学式
C15H17NSe
mdl
——
分子量
290.267
InChiKey
SKWWOUGPMWONOB-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):
    2.83
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

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:
    N,N-二乙基-2-萘甲酰胺草酰氯 、 LiAlHSeH 作用下, 以 乙醚四氢呋喃 为溶剂, 反应 7.0h, 以54%的产率得到N,N-diethyl-2-selenonaphthylamide
    参考文献:
    名称:
    Tertiary selenoamide compounds are useful superoxide radical scavengers in vitro
    摘要:
    We investigated the scavenging effects of tertiary selenoamide compounds for super oxide radicals using a highly sensitive and quantitative chemiluminescence method. At 333 nM, tertiary selenoamide compounds scavenged 25.8-81.6% of O-2(-.).N-(Phenylselenocarbonyl) piperidine was the most effective scavenger of superoxide radicals. While N,N-diethyl-2-selenonaphthylamide and N,N-diethyl-4-chloroselenobenzamide was a moderately effective scavenger of superoxide radicals. The IC50 of N-(phenylselenocarbonyl) piperidine and N,N-diethyl-2-selenonaphthylamide were determined to be 110 and 182 nM, respectively. The results suggest that tertiary selenoamide compounds are useful scavengers of superoxide radicals. (C) 2004 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ejps.2004.04.011
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文献信息

  • Tertiary selenoamide compounds are useful superoxide radical scavengers in vitro
    作者:Hitoe Takahashi、Atsuyoshi Nishina、Hirokazu Kimura、Kenji Motoki、Mamoru Koketsu、Hideharu Ishihara
    DOI:10.1016/j.ejps.2004.04.011
    日期:2004.11
    We investigated the scavenging effects of tertiary selenoamide compounds for super oxide radicals using a highly sensitive and quantitative chemiluminescence method. At 333 nM, tertiary selenoamide compounds scavenged 25.8-81.6% of O-2(-.).N-(Phenylselenocarbonyl) piperidine was the most effective scavenger of superoxide radicals. While N,N-diethyl-2-selenonaphthylamide and N,N-diethyl-4-chloroselenobenzamide was a moderately effective scavenger of superoxide radicals. The IC50 of N-(phenylselenocarbonyl) piperidine and N,N-diethyl-2-selenonaphthylamide were determined to be 110 and 182 nM, respectively. The results suggest that tertiary selenoamide compounds are useful scavengers of superoxide radicals. (C) 2004 Elsevier B.V. All rights reserved.
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