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Ethyl 1-(2-phenylquinazolin-4-yl)piperidine-3-carboxylate | 1391611-34-9

中文名称
——
中文别名
——
英文名称
Ethyl 1-(2-phenylquinazolin-4-yl)piperidine-3-carboxylate
英文别名
ethyl 1-(2-phenylquinazolin-4-yl)piperidine-3-carboxylate
Ethyl 1-(2-phenylquinazolin-4-yl)piperidine-3-carboxylate化学式
CAS
1391611-34-9
化学式
C22H23N3O2
mdl
——
分子量
361.444
InChiKey
MATIPRBVRDMSJU-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):
    4.4
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    55.3
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    参考文献:
    名称:
    Design, synthesis and biological evaluation of novel quinazoline derivatives as potential anti-cancer agents
    摘要:
    Twenty-two quinazoline derivatives have been synthesised and examined for their anti-tumour activity against three tumour cell lines, namely human breast cancer cell line (MCF-7), human cervical cancer cell line (HeLa) and human hepatoma cell line (HepG2). Twelve of the tested compounds have shown promising anti-tumour activity with an IC50 range of 5.0-9.7 mu g/mL. Regarding the spectrum of activity, five compounds exhibited interesting anti-proliferative properties against the three tested cell lines comparable to the reference drug (dasatinib).
    DOI:
    10.3109/14756366.2011.601302
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文献信息

  • Design, synthesis and biological evaluation of novel quinazoline derivatives as potential anti-cancer agents
    作者:Ahmed M. Alafeefy、Abdelkader E. Ashour
    DOI:10.3109/14756366.2011.601302
    日期:2012.8.1
    Twenty-two quinazoline derivatives have been synthesised and examined for their anti-tumour activity against three tumour cell lines, namely human breast cancer cell line (MCF-7), human cervical cancer cell line (HeLa) and human hepatoma cell line (HepG2). Twelve of the tested compounds have shown promising anti-tumour activity with an IC50 range of 5.0-9.7 mu g/mL. Regarding the spectrum of activity, five compounds exhibited interesting anti-proliferative properties against the three tested cell lines comparable to the reference drug (dasatinib).
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