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N-Benzylcanadinium | 120152-03-6

中文名称
——
中文别名
——
英文名称
N-Benzylcanadinium
英文别名
13-Benzyl-16,17-dimethoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaene
N-Benzylcanadinium化学式
CAS
120152-03-6
化学式
C27H28NO4
mdl
——
分子量
430.524
InChiKey
ZTCXXLUNOLOKTQ-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):
    4.6
  • 重原子数:
    32
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    小檗碱盐酸 作用下, 反应 5.0h, 生成 N-Benzylcanadinium
    参考文献:
    名称:
    Synthesis and antihyperglycemic evaluation of various protoberberine derivatives
    摘要:
    Various berberine derivatives (2-17) were synthesized and their antihyperglycemic activities were evaluated in a model of beta-cell-membrane chromatography and a model of alloxan-induced diabetes mice. The results indicated that compounds 5 and 14 exhibited antihyperglycemic activity. Their structure-activity relationships were discussed. (C) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.11.045
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文献信息

  • COMPOUNDS AND METHODS FOR MODULATING RHO GTPASES
    申请人:Leblond Bertrand
    公开号:US20100120810A1
    公开(公告)日:2010-05-13
    The present invention relates to methods and compositions that affect the GTP-binding activity of members of the Rho family GTPases, preferably Rac GTPases (Rac1, Rac1b, Rac2 and/or Rac3).
    本发明涉及影响Rho家族GTP酶成员的GTP结合活性的方法和组合物,优选是Rac GTP酶(Rac1,Rac1b,Rac2和/或Rac3)。
  • Synthesis and antihyperglycemic evaluation of various protoberberine derivatives
    作者:Xiaoli Bian、Langchong He、Guangde Yang
    DOI:10.1016/j.bmcl.2005.11.045
    日期:2006.3
    Various berberine derivatives (2-17) were synthesized and their antihyperglycemic activities were evaluated in a model of beta-cell-membrane chromatography and a model of alloxan-induced diabetes mice. The results indicated that compounds 5 and 14 exhibited antihyperglycemic activity. Their structure-activity relationships were discussed. (C) 2005 Elsevier Ltd. All rights reserved.
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