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N-(3-N'-morpholino-1-propyl)-3-nitro-1,8-naphthalimide | 107097-11-0

中文名称
——
中文别名
——
英文名称
N-(3-N'-morpholino-1-propyl)-3-nitro-1,8-naphthalimide
英文别名
2-(3-Morpholin-4-ylpropyl)-5-nitrobenzo[de]isoquinoline-1,3-dione
N-(3-N'-morpholino-1-propyl)-3-nitro-1,8-naphthalimide化学式
CAS
107097-11-0
化学式
C19H19N3O5
mdl
——
分子量
369.377
InChiKey
IPHQMEZATQRREA-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
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    95.7
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 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:
    N-(3-N'-morpholino-1-propyl)-3-nitro-1,8-naphthalimide 在 palladium on activated charcoal 氢气 作用下, 以 乙醇 为溶剂, 反应 4.0h, 以75%的产率得到N-(3-N'-morpholino-1-propyl)-3-amino-1,8-naphthalimide
    参考文献:
    名称:
    Synthesis and fluorescence ofN-substituted-1,8-naphthalimides
    摘要:
    AbstractA number of novel N‐substituted‐1,8‐naphthalimides have been prepared and their fluorescence yields measured in water at pH 7.4. The type of substitutent and the substitution pattern on the naphthalimide nucleus produce markedly different fluorescence yields, (quantum efficiencies, ø varying from ø = 0‐0037 for N‐(3‐N'‐morpholino‐1‐propyl)‐4‐amino‐3‐methoxy‐1,8‐naphthalirnide (7) to ø = 0–77 for N‐(3‐bromopropyl)‐4‐acetamido‐1,8‐naphthalimide (31).
    DOI:
    10.1002/jhet.5570230337
  • 作为产物:
    描述:
    N-(3-氨丙基)吗啉3-硝基-1,8-萘二甲酸酐乙醇 为溶剂, 反应 4.0h, 以69%的产率得到N-(3-N'-morpholino-1-propyl)-3-nitro-1,8-naphthalimide
    参考文献:
    名称:
    Synthesis and fluorescence ofN-substituted-1,8-naphthalimides
    摘要:
    AbstractA number of novel N‐substituted‐1,8‐naphthalimides have been prepared and their fluorescence yields measured in water at pH 7.4. The type of substitutent and the substitution pattern on the naphthalimide nucleus produce markedly different fluorescence yields, (quantum efficiencies, ø varying from ø = 0‐0037 for N‐(3‐N'‐morpholino‐1‐propyl)‐4‐amino‐3‐methoxy‐1,8‐naphthalirnide (7) to ø = 0–77 for N‐(3‐bromopropyl)‐4‐acetamido‐1,8‐naphthalimide (31).
    DOI:
    10.1002/jhet.5570230337
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文献信息

  • Methods of modulating neurotrophin-mediated activity
    申请人:Babinski Kazimierz
    公开号:US20070093474A1
    公开(公告)日:2007-04-26
    Disclosed are compositions which modulate the interaction with nerve growth factor and precursors thereof with neurotrophic receptors. Also disclosed are methods of using the compositions of the invention, including methods of administration.
    本发明涉及一种调节神经生长因子及其前体与神经营养受体相互作用的组合物。本发明还涉及使用该组合物的方法,包括给药方法。
  • METHODS OF MODULATING NEUROTROPHIN-MEDIATED ACTIVITY
    申请人:PainCeptor Pharma Corp.
    公开号:EP1931637A2
    公开(公告)日:2008-06-18
  • US7579468B2
    申请人:——
    公开号:US7579468B2
    公开(公告)日:2009-08-25
  • [EN] METHODS OF MODULATING NEUROTROPHIN-MEDIATED ACTIVITY<br/>[FR] METHODES PERMETTANT DE MODULER L'ACTIVITE INDUITE PAR LA NEUROTROPHINE
    申请人:PAINCEPTOR PHARMA CORP
    公开号:WO2007030940A2
    公开(公告)日:2007-03-22
    [EN] Disclosed are compositions which modulate the interaction with nerve growth factor and precursors thereof with neurotrophic receptors. Also disclosed are methods of using the compositions of the invention, including methods of administration.
    [FR] L'invention concerne des compositions qui modulent l'interaction entre le facteur de croissance des nerfs et ses précurseurs et les récepteurs neurotrophiques. L'invention concerne également des méthodes destinées à l'utilisation de ces compositions, ainsi que des méthodes d'administration associées.
  • Synthesis and fluorescence of<i>N</i>-substituted-1,8-naphthalimides
    作者:Richard W. Middleton、John Parrick、Eric D. Clarke、Peter Wardman
    DOI:10.1002/jhet.5570230337
    日期:1986.5
    AbstractA number of novel N‐substituted‐1,8‐naphthalimides have been prepared and their fluorescence yields measured in water at pH 7.4. The type of substitutent and the substitution pattern on the naphthalimide nucleus produce markedly different fluorescence yields, (quantum efficiencies, ø varying from ø = 0‐0037 for N‐(3‐N'‐morpholino‐1‐propyl)‐4‐amino‐3‐methoxy‐1,8‐naphthalirnide (7) to ø = 0–77 for N‐(3‐bromopropyl)‐4‐acetamido‐1,8‐naphthalimide (31).
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