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2-(5-methylthiophen-2-yl)-3-phenyl-1-propyl-2H-quinazolin-4-one | 1429192-42-6

中文名称
——
中文别名
——
英文名称
2-(5-methylthiophen-2-yl)-3-phenyl-1-propyl-2H-quinazolin-4-one
英文别名
——
2-(5-methylthiophen-2-yl)-3-phenyl-1-propyl-2H-quinazolin-4-one化学式
CAS
1429192-42-6
化学式
C22H22N2OS
mdl
——
分子量
362.495
InChiKey
WNWCBUHBVXNKTE-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):
    5.5
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    51.8
  • 氢给体数:
    0
  • 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

反应信息

  • 作为产物:
    描述:
    2’-氨基苯甲酰苯胺 在 sodium hydride 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 3.5h, 生成 2-(5-methylthiophen-2-yl)-3-phenyl-1-propyl-2H-quinazolin-4-one
    参考文献:
    名称:
    N-Methyldihydroquinazolinone Derivatives of Retro-2 with Enhanced Efficacy against Shiga Toxin
    摘要:
    The Retro-2 molecule protects cells against Shiga toxins by specifically blocking retrograde transport from early endosomes to the trans-Golgi network A SAR study has been carried out to identify more potent compounds. Cyclization and modifications of Retro-2 led to a compound with roughly 100 fold improvement of the EC50 against Shiga toxin cytotoxicity measured in a cell protein synthesis assay. We also demonstrated that only one enantiomer of the dihydroquinazolinone reported herein is bioactive.
    DOI:
    10.1021/jm4002346
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文献信息

  • <i>N</i>-Methyldihydroquinazolinone Derivatives of Retro-2 with Enhanced Efficacy against Shiga Toxin
    作者:Romain Noel、Neetu Gupta、Valérie Pons、Amélie Goudet、Maria Daniela Garcia-Castillo、Aurélien Michau、Jennifer Martinez、David-Alexandre Buisson、Ludger Johannes、Daniel Gillet、Julien Barbier、Jean-Christophe Cintrat
    DOI:10.1021/jm4002346
    日期:2013.4.25
    The Retro-2 molecule protects cells against Shiga toxins by specifically blocking retrograde transport from early endosomes to the trans-Golgi network A SAR study has been carried out to identify more potent compounds. Cyclization and modifications of Retro-2 led to a compound with roughly 100 fold improvement of the EC50 against Shiga toxin cytotoxicity measured in a cell protein synthesis assay. We also demonstrated that only one enantiomer of the dihydroquinazolinone reported herein is bioactive.
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