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8-Nitro-5-[[5-(phenoxymethyl)-4-phenyl-1,2,4-triazol-3-yl]sulfanyl]quinoline

中文名称
——
中文别名
——
英文名称
8-Nitro-5-[[5-(phenoxymethyl)-4-phenyl-1,2,4-triazol-3-yl]sulfanyl]quinoline
英文别名
——
8-Nitro-5-[[5-(phenoxymethyl)-4-phenyl-1,2,4-triazol-3-yl]sulfanyl]quinoline化学式
CAS
——
化学式
C24H17N5O3S
mdl
——
分子量
455.5
InChiKey
CAYNCODJBVZVDW-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):
    5.1
  • 重原子数:
    33
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    124
  • 氢给体数:
    0
  • 氢受体数:
    7

文献信息

  • Compositions and methods for modulating sirtuin activity
    申请人:Kazantsev Aleksey G.
    公开号:US20080021063A1
    公开(公告)日:2008-01-24
    The present invention is based, in part, on our discovery of compounds that inhibit an activity of a sirtuin (e.g., compounds that inhibit or preferentially inhibit an activity of SIRT2) and are therefore believed useful in the treatment or prevention of diseases associated with sirtuin activity. These diseases include, but are not limited to, neurological disorders such as Parkinson's Disease (PD).
  • COMPOSITIONS AND METHODS FOR MODULATING SIRTUIN ACTIVITY
    申请人:Kazantsev Aleksey G.
    公开号:US20090259044A1
    公开(公告)日:2009-10-15
    The present invention is based, in part, on our discovery of compounds that inhibit an activity of a sirtuin (e.g., compounds that inhibit or preferentially inhibit an activity of SIRT2) and are therefore believed useful in the treatment or prevention of diseases associated with sirtuin activity. These diseases include, but are not limited to, neurological disorders such as Parkinson's Disease (PD).
  • SMALL MOLECULE ACTIVATORS OF NRF2 PATHWAY
    申请人:THE GENERAL HOSPITAL CORPORATION
    公开号:US20160101098A1
    公开(公告)日:2016-04-14
    This disclosure relates to compounds that act as activators of the NRF2/KEAP1/ARE pathway. Specifically, the compounds provided herein can act as high affinity reversible bindings for the NRF2 inhibitor, KEAP1. In some cases, NRF2/KEAP1/ARE pathway activation compounds are capable of repressing expression of inflammatory markers and/or reducing levels of TNFa to provide neuroprotective anti-inflammatory effects in the CNS. Such compounds are useful in the treatment of a variety of diseases including Huntington's disease, Parkinson's disease, Alzheimer's disease, inflammation, and cancer.
  • US8153803B2
    申请人:——
    公开号:US8153803B2
    公开(公告)日:2012-04-10
  • US9737525B2
    申请人:——
    公开号:US9737525B2
    公开(公告)日:2017-08-22
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同类化合物

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