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2-((di(methyl-13C)amino)methyl)quinolin-8-ol | 1428417-50-8

中文名称
——
中文别名
——
英文名称
2-((di(methyl-13C)amino)methyl)quinolin-8-ol
英文别名
——
2-((di(methyl-13C)amino)methyl)quinolin-8-ol化学式
CAS
1428417-50-8
化学式
C12H14N2O
mdl
——
分子量
204.234
InChiKey
VEEBMVNHFKHDHV-ZDOIIHCHSA-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):
    2.0
  • 重原子数:
    15.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    36.36
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

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

反应信息

  • 作为产物:
    描述:
    8-羟基喹啉-2-甲醛Dimethylamine-13C2 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 2.0h, 生成 2-((di(methyl-13C)amino)methyl)quinolin-8-ol
    参考文献:
    名称:
    Mixed Ligand Cu2+ Complexes of a Model Therapeutic with Alzheimer’s Amyloid-β Peptide and Monoamine Neurotransmitters
    摘要:
    8-Hydroxyquinolines (8HQ) have found widespread application in chemistry and biology due to their ability to complex a range of transition metal ions. The family of 2-substituted 8HQs has been proposed for use in the treatment of Alzheimer's disease (AD). Most notably, the therapeutic PBT2 (Prana Biotechnology Ltd.) has been shown to act as an efficient metal chaperone, disaggregate metal-enriched amyloid plaques comprised of the A beta peptide, inhibit Cu/A beta redox chemistry, and reverse the AD phenotype in transgenic animal models. Yet surprisingly little is known about the molecular interactions at play. In this study, we show that the homologous ligand 2-[(dimethylamino)methyl]-8-hydroxyquinoline (HL) forms a CuL complex with a conditional (apparent) dissociation constant of 0.33 nM at pH 6.9 and is capable of forming ternary Cu2+ complexes with neurotransmitters including histamine (HA), glutamic acid (Glu), and glycine (Gly), with glutathione disulfide (GSSG), and with histidine (His) side chains of proteins and peptides including the A beta peptide. Our findings suggest a molecular basis for the strong metal chaperone activity of PBT2, its ability to attenuate Cu2+/A beta interactions, and its potential to promote neuroprotective and neuroregenerative effects.
    DOI:
    10.1021/ic302289r
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