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O-Methyldemethylendeoxynybomycin | 50553-58-7

中文名称
——
中文别名
——
英文名称
O-Methyldemethylendeoxynybomycin
英文别名
10-methoxy-1,4,6-trimethyl-1H,9H-pyrido[3,2-g]quinoline-2,8-dione;10-methoxy-1,4,6-trimethylpyrido[3.2-g]quinoline-2,8(1H,9H)-dione;10-methoxy-1,4,6-trimethyl-9H-pyrido[3,2-g]quinoline-2,8-dione
O-Methyldemethylendeoxynybomycin化学式
CAS
50553-58-7
化学式
C16H16N2O3
mdl
——
分子量
284.315
InChiKey
KFXFRVCZRBQTQH-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

物化性质

  • 沸点:
    511.6±50.0 °C(Predicted)
  • 密度:
    1.237±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.7
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    58.6
  • 氢给体数:
    1
  • 氢受体数:
    3

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • CDC25 inhibitors
    申请人:InterMed Discovery GmbH
    公开号:EP2130831A1
    公开(公告)日:2009-12-09
    The invention relates to pyridoquinolones, their synthesis and pharmaceutical use. The pyridoquinolones are useful as CDC25 inhibitors.
    本发明涉及吡啶并喹啉酮及其合成和药物用途。所述吡啶并喹啉酮作为CDC25抑制剂具有应用价值。
  • Compounds and anti-tumor NQO1 substrates
    申请人:The Board of Trustees of the University of Illinois
    公开号:US10285986B2
    公开(公告)日:2019-05-14
    Compositions comprising Formula (I) can be selectively lethal toward a variety of different cancer cell types. The compositions are useful for the management, treatment, control, or adjunct treatment of diseases, where the selective lethality is beneficial in chemotherapeutic therapy.
    由式(I)组成的组合物可对多种不同类型的癌细胞产生选择性杀伤作用。这些组合物可用于疾病的管理、治疗、控制或辅助治疗,其中选择性致死在化疗中是有益的。
  • Chemistry and Biology of Deoxynyboquinone, a Potent Inducer of Cancer Cell Death
    作者:Joseph S. Bair、Rahul Palchaudhuri、Paul J. Hergenrother
    DOI:10.1021/ja100610m
    日期:2010.4.21
    Deoxynyboquinone (DNQ) is a potent antineoplastic agent with an unknown mechanism of action. Here we describe a facile synthetic route to this anthraquinone, and we use this material to determine the mechanism by which DNQ induces death in cancer cells. DNQ was synthesized in seven linear steps through a route employing three palladium-mediated coupling reactions. Experiments performed on cancer cells grown in hypoxia and normoxia strongly suggest that DNQ undergoes bioreduction to its semiquinone, which then is re-oxidized by molecular oxygen, forming superoxide that induces cell death. Furthermore, global transcript profiling of cells treated with DNQ shows elevation of transcripts related to oxidative stress, a result confirmed at the protein level by Western blotting. In contrast to most other antineoplastic agents that generate reactive oxygen species (ROS), DNQ potently induces death of cancer cells in culture, with IC50 values between 16 and 210 nM. In addition, unlike the experimental therapeutic elesclomol, DNQ is still able to induce cancer cell death under hypoxic conditions. This mechanistic understanding of DNQ will allow for a more comprehensive evaluation of the potential of direct ROS generation as an anticancer strategy, and DNQ itself has potential as a novel anticancer agent.
  • US9611266B2
    申请人:——
    公开号:US9611266B2
    公开(公告)日:2017-04-04
  • [EN] COMPOUNDS AND ANTI-TUMOR NQO1 SUBSTRATES<br/>[FR] COMPOSÉS ET SUBSTRATS ANTITUMORAUX NQO1
    申请人:UNIV ILLINOIS
    公开号:WO2013056073A1
    公开(公告)日:2013-04-18
    Compounds of Formula (I) can be selectively lethal toward a variety of different cancer cell types. The compounds are useful for the management, treatment, control, or adjunct treatment of diseases, where the selective lethality is beneficial in chemotherapeutic therapy.
    化合物的化学式(I)可以选择性地对多种不同类型的癌细胞具有致命作用。这些化合物对于管理、治疗、控制或辅助治疗疾病非常有用,其中选择性的致命作用在化疗疗法中具有益处。
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