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2,3-Bis-bromomethyl-6-methoxy-quinoxaline 1,4-dioxide | 36708-65-3

中文名称
——
中文别名
——
英文名称
2,3-Bis-bromomethyl-6-methoxy-quinoxaline 1,4-dioxide
英文别名
2,3-Bis(bromomethyl)-6-methoxy-4-oxidoquinoxalin-1-ium 1-oxide
2,3-Bis-bromomethyl-6-methoxy-quinoxaline 1,4-dioxide化学式
CAS
36708-65-3
化学式
C11H10Br2N2O3
mdl
——
分子量
378.02
InChiKey
HURSFJLOXJGWTG-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):
    1
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    55.6
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • JP2011037776A
    申请人:——
    公开号:JP2011037776A
    公开(公告)日:2011-02-24
  • PHARMACEUTICAL COMPOSITION COMPRISING SUBSTANCE INHIBITING ENZYMATIC ACTIVITY OF PEROXIREDOXIN 2 AS EFFECTIVE INGREDIENT FOR TREATMENT OF COLORECTAL CANCER
    申请人:EWHA UNIVERSITY - INDUSTRY COLLABORATION FOUNDATION
    公开号:US20200129508A1
    公开(公告)日:2020-04-30
    The present invention relates to a pharmaceutical composition for treating colorectal cancer including a material inhibiting the enzyme activity of peroxiredoxin 2 as an active ingredient, and more specifically, to a pharmaceutical composition for treating colorectal cancer, which exhibits the effect of reducing colon polyps via increase of active β-catenin degradation by inhibiting the activity of peroxiredoxin 2, based on the mechanism that promotes colorectal tumor by the interaction between peroxiredoxin 2 (PrxII) and tankyrase (TNKS) in an APC-mutant cell.
  • [EN] PHARMACEUTICAL COMPOSITION COMPRISING SUBSTANCE INHIBITING ENZYMATIC ACTIVITY OF PEROXIREDOXIN 2 AS EFFECTIVE INGREDIENT FOR TREATMENT OF COLORECTAL CANCER<br/>[FR] COMPOSITION PHARMACEUTIQUE COMPRENANT UNE SUBSTANCE INHIBANT L'ACTIVITÉ ENZYMATIQUE DE LA PEROXYRÉDOXINE 2 EN TANT QUE PRINCIPE ACTIF POUR LE TRAITEMENT DU CANCER COLORECTAL<br/>[KO] 퍼록시레독신 2 의 효소 활성을 억제하는 물질을 유효 성분으로 포함하는 대장암 치료용 약학적 조성물
    申请人:UNIV EWHA IND COLLABORATION
    公开号:WO2019004732A1
    公开(公告)日:2019-01-03
    본 발명은 퍼록시레독신 2 의 효소 활성을 억제하는 물질을 유효 성분으로 함유하는 대장암 치료용 약학적 조성물에 관한 것으로, 보다 상세하게는 APC 돌연변이 세포에서 퍼록시레독신 2(Prx II) 가 탄키라제(Tankyrase, TNKS)와 상호작용하여 대장암 종양을 촉진하는 메커니즘에 기초하여, 퍼록시레독신 2의 활성을 억제함으로서 활성 베타카테닌 분해를 증가시켜 대장 용종을 감소시키는 효과를 나타내는 대장암 치료용 약학적 조성물에 관한 것이다.
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