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N-(2-acetylaminoethyl)-1,6-dideoxynojirimycin | 936567-50-9

中文名称
——
中文别名
——
英文名称
N-(2-acetylaminoethyl)-1,6-dideoxynojirimycin
英文别名
N-[2-[(2R,3R,4R,5S)-3,4,5-trihydroxy-2-methylpiperidin-1-yl]ethyl]acetamide
N-(2-acetylaminoethyl)-1,6-dideoxynojirimycin化学式
CAS
936567-50-9
化学式
C10H20N2O4
mdl
——
分子量
232.28
InChiKey
XSTCOQQAVYQKBC-XCWAXFADSA-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):
    -2.1
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    93
  • 氢给体数:
    4
  • 氢受体数:
    5

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-(2-aminoethyl)-1,6-dideoxynojirimycin乙酸酐吡啶sodium methylate 作用下, 以 甲醇 为溶剂, 反应 5.33h, 以95%的产率得到N-(2-acetylaminoethyl)-1,6-dideoxynojirimycin
    参考文献:
    名称:
    An expeditious one-pot synthesis of 1,6-dideoxy-N-alkylated nojirimycin derivatives and their inhibitory effects on the secretion of IFN-γ and IL-4
    摘要:
    An efficient 'one-pot' approach to the synthesis of 1,6-dideoxy-N-alkylated nojirimycin derivatives in good yields and with high stereoselectivity was developed. It was found that the synthetic N-alkylated iminosugars showed inhibitory effects on the release of the cytokines IFN-gamma and IL-4 from the mouse splenocytes. The preliminary structure-activity relationship was deduced from the activities of N-substituted iminosugars. Apart from the cytokine inhibitory activities, a series of glycosidase inhibitory activities were also examined. The present experimental data demonstrated that synthetic iminosugars might hold potential as immunosuppressive agents. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.11.036
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文献信息

  • An expeditious one-pot synthesis of 1,6-dideoxy-N-alkylated nojirimycin derivatives and their inhibitory effects on the secretion of IFN-γ and IL-4
    作者:Jian Zhou、Yongmin Zhang、Xia Zhou、Jing Zhou、Li-He Zhang、Xin-Shan Ye、Xiao-Lian Zhang
    DOI:10.1016/j.bmc.2007.11.036
    日期:2008.2.15
    An efficient 'one-pot' approach to the synthesis of 1,6-dideoxy-N-alkylated nojirimycin derivatives in good yields and with high stereoselectivity was developed. It was found that the synthetic N-alkylated iminosugars showed inhibitory effects on the release of the cytokines IFN-gamma and IL-4 from the mouse splenocytes. The preliminary structure-activity relationship was deduced from the activities of N-substituted iminosugars. Apart from the cytokine inhibitory activities, a series of glycosidase inhibitory activities were also examined. The present experimental data demonstrated that synthetic iminosugars might hold potential as immunosuppressive agents. (C) 2007 Elsevier Ltd. All rights reserved.
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