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3,8-diethyl-2-phenyl-4H-pyrido[1,2-a]pyrimidin-4-one | 1338923-03-7

中文名称
——
中文别名
——
英文名称
3,8-diethyl-2-phenyl-4H-pyrido[1,2-a]pyrimidin-4-one
英文别名
3,8-Diethyl-2-phenylpyrido[1,2-a]pyrimidin-4-one
3,8-diethyl-2-phenyl-4H-pyrido[1,2-a]pyrimidin-4-one化学式
CAS
1338923-03-7
化学式
C18H18N2O
mdl
——
分子量
278.354
InChiKey
QQDSFYRDIKEDBS-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):
    2.9
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    32.7
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2-氨基-4-乙基吡啶2-乙氧甲酰苯丁酮 在 polyphosphorus acid 作用下, 反应 1.0h, 生成 3,8-diethyl-2-phenyl-4H-pyrido[1,2-a]pyrimidin-4-one
    参考文献:
    名称:
    Identification of Pyrido[1,2-α]pyrimidine-4-ones as New Molecules Improving the Transcriptional Functions of Estrogen-Related Receptor α
    摘要:
    The nuclear estrogen-related receptor alpha (ERR alpha) plays a central role in the regulation of expression of the genes involved in mitochondrial biogenesis and oxidative metabolism. We have successfully identified a series of pyrido [1,2-alpha]pyrimidin-4-ones as new agonists enhancing the transcriptional functions of ERRa. The compounds potently elevated the m RNA levels and the protein levels of ERRa downstream targets. Consequently, the compounds improved the glucose and fatty acid uptake in C2C12 muscle cells.
    DOI:
    10.1021/jm200976s
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文献信息

  • Identification of Pyrido[1,2-α]pyrimidine-4-ones as New Molecules Improving the Transcriptional Functions of Estrogen-Related Receptor α
    作者:Lijie Peng、Xuefei Gao、Lei Duan、Xiaomei Ren、Donghai Wu、Ke Ding
    DOI:10.1021/jm200976s
    日期:2011.11.10
    The nuclear estrogen-related receptor alpha (ERR alpha) plays a central role in the regulation of expression of the genes involved in mitochondrial biogenesis and oxidative metabolism. We have successfully identified a series of pyrido [1,2-alpha]pyrimidin-4-ones as new agonists enhancing the transcriptional functions of ERRa. The compounds potently elevated the m RNA levels and the protein levels of ERRa downstream targets. Consequently, the compounds improved the glucose and fatty acid uptake in C2C12 muscle cells.
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