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2-Methyl-4-[4-(2-methylquinolin-4-yl)-1,4-diazepan-1-yl]quinoline

中文名称
——
中文别名
——
英文名称
2-Methyl-4-[4-(2-methylquinolin-4-yl)-1,4-diazepan-1-yl]quinoline
英文别名
——
2-Methyl-4-[4-(2-methylquinolin-4-yl)-1,4-diazepan-1-yl]quinoline化学式
CAS
——
化学式
C25H26N4
mdl
——
分子量
382.5
InChiKey
KDXKTBLLOZDBKK-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):
    5.3
  • 重原子数:
    29
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    32.3
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • Spiroisoquinoline compound, a method for preparing the same and an intermediate thereof
    申请人:——
    公开号:US20040106635A1
    公开(公告)日:2004-06-03
    The present invention provides a novel spiroistiquinoline derivative of the formula [I]: which has a small-conductance potassium channel (SK) blocking activity and is useful as a medicament, a method for preparing the same and an intermediate thereof. 1
    本发明提供了一种新的螺环异喹啉生物,其化学式为[I]:具有小电导通道(SK)阻滞活性,可用作药物,提供其制备方法和中间体。1
  • Pyrazolopyrimidine compound and a process for preparing the same
    申请人:Takamuro Iwao
    公开号:US20060135525A1
    公开(公告)日:2006-06-22
    The present invention provides a novel pyrazolopyrimidine compound of the formula [I]: wherein R′ is (A) a substituted aryl group, (B) an optionally substituted nitrogen-containing aliphatic heteromonocyclic group, (C) a substituted cyclo-lower alkyl group, (D) an optionally substituted amino group, or (E) a substituted heteroaryl group, R 2 is (a) an optionally substituted heteroaryl group or (b) an optionally substituted aryl group, Y is a single bond, a lower alkylene group or a lower alkenylene group, Z is a group of the formula: —CO—, —CH2-, S02- or a group of the formula [II]: Q is a lower alkylene group, and q is an integer of 0 or 1 or a pharmaceutically acceptable sait thereof, which has a small conductance potassium channel (SK channel) blocking activity and is useful as a medicament and a process for preparing the same.
    本发明提供了一种新型的吡唑嘧啶化合物,其化学式为[I]:其中R′为(A)取代芳基,(B)可选取代的含氮脂肪杂环基,(C)取代的环低烷基,(D)可选取代的基或(E)取代的杂环芳基;R2为(a)可选取代的杂环芳基或(b)可选取代的芳基;Y为单键,低碳基烷基或低碳基烯基;Z为式[II]的基团:其中Q为低碳基烷基,q为0或1的整数,或其药学上可接受的盐。该化合物具有小电导通道(SK通道)阻滞活性,并可作为药物使用,以及其制备方法。
  • Nitrogenous Fused Bicyclic Compound
    申请人:Takamuro Iwao
    公开号:US20080081817A1
    公开(公告)日:2008-04-03
    A novel nitrogenous fused bicyclic compound represented by the following general formula [1] or a pharmacologically acceptable salt of the compound. They have excellent SK channel blocking activity and are useful as a medicine. [I] (In the formula, R 0 represents hydrogen, halogeno, etc.; R 1 represents a group represented by the formula (a) or (b); A represents a group represented by the formula (X) or (Y); D 1 , D 2 and D 3 each represents N or CH; R 2 represents halogeno or optionally halogenated lower alkyl, etc.; R 3 represents hydrogen or lower alkyl; and Q represents lower alkylene.)
    下面是一种新型的含氮融合双环化合物,其通式如下[1],或其药理学上可接受的盐。它们具有出色的SK通道阻滞活性,是一种有用的药物。[I](在公式中,R0代表氢,卤素等; R1代表由公式(a)或(b)表示的基团; A代表由公式(X)或(Y)表示的基团; D1,D2和D3分别表示N或CH; R2代表卤素或可选卤代的低碳基等; R3代表氢或低碳基; Q代表低碳链基)。
  • NITROGENOUS FUSED BICYCLIC COMPOUND
    申请人:TANABE SEIYAKU CO., LTD.
    公开号:EP1772454A1
    公开(公告)日:2007-04-11
    A novel nitrogenous fused bicyclic compound represented by the following general formula [1] or a pharmacologically acceptable salt of the compound. They have excellent SK channel blocking activity and are useful as a medicine. [I] (In the formula, R0 represents hydrogen, halogeno, etc.; R1 represents a group represented by the formula (a) or (b); A represents a group represented by the formula (X) or (Y); D1, D2 and D3 each represents N or CH; R2 represents halogeno or optionally halogenated lower alkyl, etc.; R3 represents hydrogen or lower alkyl; and Q represents lower alkylene.)
    一种由以下通式[1]代表的新型含氮融合双环化合物或其药理学上可接受的盐。它们具有优异的 SK 通道阻断活性,可用作药物。[I](式中,R0 代表氢、卤素等;R1 代表由式(a)或(b)表示的基团;A 代表由式(X)或(Y)表示的基团;D1、D2 和 D3 各自代表 N 或 CH;R2 代表卤素或任选卤化的低级烷基等;R3 代表氢或低级烷基;Q 代表低级亚烷基)。
  • SPIROISOQUINOLINE COMPOUNDS, METHODS FOR THEIR PREPARATION AND INTERMEDIATES THEREOF
    申请人:TANABE SEIYAKU CO., LTD.
    公开号:EP1373247A2
    公开(公告)日:2004-01-02
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