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(S)-tert-butyl 1-(2-(2,5-dimethoxy-3,6-dioxocyclohexa-1,4-dienyl)ethylamino)-1-oxopropan-2-ylcarbamate | 1380092-22-7

中文名称
——
中文别名
——
英文名称
(S)-tert-butyl 1-(2-(2,5-dimethoxy-3,6-dioxocyclohexa-1,4-dienyl)ethylamino)-1-oxopropan-2-ylcarbamate
英文别名
tert-butyl N-[(2S)-1-[2-(2,5-dimethoxy-3,6-dioxocyclohexa-1,4-dien-1-yl)ethylamino]-1-oxopropan-2-yl]carbamate
(S)-tert-butyl 1-(2-(2,5-dimethoxy-3,6-dioxocyclohexa-1,4-dienyl)ethylamino)-1-oxopropan-2-ylcarbamate化学式
CAS
1380092-22-7
化学式
C18H26N2O7
mdl
——
分子量
382.414
InChiKey
ZPTNVYDPBXYWLJ-JTQLQIEISA-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):
    1.1
  • 重原子数:
    27
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    120
  • 氢给体数:
    2
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    (S)-tert-butyl 1-(2-(2,5-dimethoxy-3,6-dioxocyclohexa-1,4-dienyl)ethylamino)-1-oxopropan-2-ylcarbamate盐酸 作用下, 以 甲醇 为溶剂, 反应 48.0h, 以82%的产率得到(S)-1-(2-(2,5-dihydroxy-3,6-dioxocyclohexa-1,4-dienyl)ethylamino)-1-oxopropan-2-aminium chloride
    参考文献:
    名称:
    Synthesis and biological evaluation of hydrophilic embelin derivatives
    摘要:
    In continuance of our search for newer anti-cancer agents we were interested on embelin, a XIAP (X-linked inhibitor of apoptosis protein) inhibitor. This natural benzoquinone bear a lipophilic chain and we report here the synthesis of hydrophilic analogues of embelin. To allow a large flexibility in the nature of the hydrophilic group, three amines with different length of carbon chain bearing a protected benzoquinone were prepared. The cytotoxic effects of these derivatives were evaluated on KB cell line. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.04.024
  • 作为产物:
    参考文献:
    名称:
    Synthesis and biological evaluation of hydrophilic embelin derivatives
    摘要:
    In continuance of our search for newer anti-cancer agents we were interested on embelin, a XIAP (X-linked inhibitor of apoptosis protein) inhibitor. This natural benzoquinone bear a lipophilic chain and we report here the synthesis of hydrophilic analogues of embelin. To allow a large flexibility in the nature of the hydrophilic group, three amines with different length of carbon chain bearing a protected benzoquinone were prepared. The cytotoxic effects of these derivatives were evaluated on KB cell line. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.04.024
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