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Benzyl 6-[[3-(3-methyl-1,4-dioxonaphthalen-2-yl)selanyl-2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]oxypropanoyl]amino]hexanoate | 1416131-01-5

中文名称
——
中文别名
——
英文名称
Benzyl 6-[[3-(3-methyl-1,4-dioxonaphthalen-2-yl)selanyl-2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]oxypropanoyl]amino]hexanoate
英文别名
benzyl 6-[[3-(3-methyl-1,4-dioxonaphthalen-2-yl)selanyl-2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]oxypropanoyl]amino]hexanoate
Benzyl 6-[[3-(3-methyl-1,4-dioxonaphthalen-2-yl)selanyl-2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]oxypropanoyl]amino]hexanoate化学式
CAS
1416131-01-5
化学式
C34H40N2O9Se
mdl
——
分子量
699.66
InChiKey
UADVYVLANGKQAJ-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):
    4.32
  • 重原子数:
    46
  • 可旋转键数:
    19
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    154
  • 氢给体数:
    2
  • 氢受体数:
    9

反应信息

  • 作为产物:
    描述:
    benzyl 6-isocyanohexanoateBOC-甘氨酸 、 2-(3-methyl-1,4-dioxo-1,4-dihydronaphthalen-2-ylselanyl)acetaldehyde 以 为溶剂, 以66%的产率得到Benzyl 6-[[3-(3-methyl-1,4-dioxonaphthalen-2-yl)selanyl-2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]oxypropanoyl]amino]hexanoate
    参考文献:
    名称:
    Novel peptidomimetic compounds containing redox active chalcogens and quinones as potential anticancer agents
    摘要:
    Many types of cancer cells are associated with a disturbed intracellular redox balance and oxidative stress (OS). Among the various agents employed to modulate the intracellular redox state of cells, certain redox catalysts containing quinone and chalcogen moieties have shown considerable promise. Passerini multicomponent reaction has been developed for the synthesis of agents combining two, three or even four redox centers in one molecule in a good yield. When incubated with cancer cells these agents inhibited cell proliferation and induced apoptotic cell death. Interestingly, some of these redox active compounds exhibited quite low toxicity with normal cells. The cause was obviously OS, which was reflected by significant decrease in reduced glutathione, subsequently cell cycle arrest and induction of apoptosis. (C) 2012 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2012.09.033
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文献信息

  • Novel peptidomimetic compounds containing redox active chalcogens and quinones as potential anticancer agents
    作者:Saad Shaaban、Randi Diestel、Bettina Hinkelmann、Yazh Muthukumar、Rajeshwar P. Verma、Florenz Sasse、Claus Jacob
    DOI:10.1016/j.ejmech.2012.09.033
    日期:2012.12
    Many types of cancer cells are associated with a disturbed intracellular redox balance and oxidative stress (OS). Among the various agents employed to modulate the intracellular redox state of cells, certain redox catalysts containing quinone and chalcogen moieties have shown considerable promise. Passerini multicomponent reaction has been developed for the synthesis of agents combining two, three or even four redox centers in one molecule in a good yield. When incubated with cancer cells these agents inhibited cell proliferation and induced apoptotic cell death. Interestingly, some of these redox active compounds exhibited quite low toxicity with normal cells. The cause was obviously OS, which was reflected by significant decrease in reduced glutathione, subsequently cell cycle arrest and induction of apoptosis. (C) 2012 Elsevier Masson SAS. All rights reserved.
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