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[4-(2-Chloro-phenoxy)-butyl]-methyl-amine | 91428-60-3

中文名称
——
中文别名
——
英文名称
[4-(2-Chloro-phenoxy)-butyl]-methyl-amine
英文别名
4-(2-chlorophenoxy)-N-methylbutan-1-amine
[4-(2-Chloro-phenoxy)-butyl]-methyl-amine化学式
CAS
91428-60-3
化学式
C11H16ClNO
mdl
——
分子量
213.707
InChiKey
KKHOWIXOWLRVRW-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):
    2.8
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    21.3
  • 氢给体数:
    1
  • 氢受体数:
    2

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

  • 作为反应物:
    描述:
    [4-(2-Chloro-phenoxy)-butyl]-methyl-amine3-溴丙炔乙醚 为溶剂, 生成 [4-(2-Chloro-phenoxy)-butyl]-methyl-prop-2-ynyl-amine
    参考文献:
    名称:
    BE626725
    摘要:
    公开号:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and antidepressant activity of substituted (.omega.-aminoalkoxy)benzene derivatives
    摘要:
    A series of substituted (omega-aminoalkoxy)benzene derivatives has been synthesized and screened for potential antidepressant activities. The effect of structural variation of these molecules has been systematically examined. Antidepressant activity was clearly displayed by 2-benzyl-1-[4-(methylamino)butoxy]benzene (7), 2-(2-hydroxybenzyl)-1-[4-(methylamino)butoxy]benzene (19), 1-[4-(methylamino)butoxy]-2-phenoxybenzene (29), and 1-[4-(methylamino)butoxy]-2-(phenylthio)benzene (31) in further pharmacological studies. These compounds did not possess the anticholinergic, antihistaminic, and muscle-relaxant side effects common to tricyclic antidepressants.
    DOI:
    10.1021/jm00134a004
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文献信息

  • Synthesis and antidepressant activity of substituted (.omega.-aminoalkoxy)benzene derivatives
    作者:Ryoji Kikumoto、Akihiro Tobe、Shinji Tonomura
    DOI:10.1021/jm00134a004
    日期:1981.2
    A series of substituted (omega-aminoalkoxy)benzene derivatives has been synthesized and screened for potential antidepressant activities. The effect of structural variation of these molecules has been systematically examined. Antidepressant activity was clearly displayed by 2-benzyl-1-[4-(methylamino)butoxy]benzene (7), 2-(2-hydroxybenzyl)-1-[4-(methylamino)butoxy]benzene (19), 1-[4-(methylamino)butoxy]-2-phenoxybenzene (29), and 1-[4-(methylamino)butoxy]-2-(phenylthio)benzene (31) in further pharmacological studies. These compounds did not possess the anticholinergic, antihistaminic, and muscle-relaxant side effects common to tricyclic antidepressants.
  • Discovery of highly potent novel antifungal azoles by structure-based rational design
    作者:Wenya Wang、Chunquan Sheng、Xiaoying Che、Haitao Ji、Yongbing Cao、Zhenyuan Miao、Jianzhong Yao、Wannian Zhang
    DOI:10.1016/j.bmcl.2009.07.144
    日期:2009.10
    On the basis of the active site of lanosterol 14 alpha-demethylase from Candida albicans (CACYP51), a series of new azoles were designed and synthesized. All the new azoles show excellent in vitro activity against most of the tested pathogenic fungi, which represent a class of promising leads for the development of novel antifungal agents. The MIC80 value of compounds 8c, 8i and 8n against C. albicans is 0.001 mu g/mL, indicating that these compounds are more potent than fluconazole, itraconazole and voriconazole. Flexible molecular docking was used to analyze the structure-activity relationships (SARs) of the compounds. The designed compounds interact with CACYP51 through hydrophobic, van der Waals and hydrogen-bonding interactions. (C) 2009 Published by Elsevier Ltd.
  • BE626725
    申请人:——
    公开号:——
    公开(公告)日:——
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