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Thiopyrano[2,3-b]quinolin-2-one | 1235162-95-4

中文名称
——
中文别名
——
英文名称
Thiopyrano[2,3-b]quinolin-2-one
英文别名
——
Thiopyrano[2,3-b]quinolin-2-one化学式
CAS
1235162-95-4
化学式
C12H7NOS
mdl
——
分子量
213.26
InChiKey
GPPLGXBJDUWEQE-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):
    3.1
  • 重原子数:
    15
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    55.3
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    3-formyl-2-mercaptoquinoline乙酰氯sodium methylate 作用下, 以92%的产率得到Thiopyrano[2,3-b]quinolin-2-one
    参考文献:
    名称:
    2-Thieno/Selenopyrano[2,3-b]quinolines: Microwave-Induced One-Pot Synthesis, DNA Binding, and Photocleavage Studies
    摘要:
    We have characterized a new class of 2-thieno/2-selenopyrano[2,3-b]quinolin-2-ol (2c/3c) intercalators exhibiting a novel type of DNA binding and photocleavage activity. The dynamic behavior of these compounds with DNA was investigated by absorption spectra (obtained K-b constant for 2c is 3.6 x 10(6) and for 3c is 2.8 x 10(5)), viscosity, and thermal denaturation studies. Intrinsic binding constants (K-b) have been estimated under a similar set of experimental conditions. An absorption spectral study shows the strong interaction between synthesized 2c, 3c, and base pairs CT-DNA. In addition, the effects of these compounds on DNA cleavage were investigated by photoirradiation at 360 nm and show that the hybrids effectively cleaved double-stranded DNA with UV light of a long wavelength and without any additive.
    DOI:
    10.1080/10426500802529622
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文献信息

  • 2-Thieno/Selenopyrano[2,3-<i>b</i>]quinolines: Microwave-Induced One-Pot Synthesis, DNA Binding, and Photocleavage Studies
    作者:H. R. Prakash Naik、H. S. Bhojya Naik、T. R. Ravikumar Naik、T. Aravinda、D. S. Lamani、H. Raja Naika
    DOI:10.1080/10426500802529622
    日期:2009.10.13
    We have characterized a new class of 2-thieno/2-selenopyrano[2,3-b]quinolin-2-ol (2c/3c) intercalators exhibiting a novel type of DNA binding and photocleavage activity. The dynamic behavior of these compounds with DNA was investigated by absorption spectra (obtained K-b constant for 2c is 3.6 x 10(6) and for 3c is 2.8 x 10(5)), viscosity, and thermal denaturation studies. Intrinsic binding constants (K-b) have been estimated under a similar set of experimental conditions. An absorption spectral study shows the strong interaction between synthesized 2c, 3c, and base pairs CT-DNA. In addition, the effects of these compounds on DNA cleavage were investigated by photoirradiation at 360 nm and show that the hybrids effectively cleaved double-stranded DNA with UV light of a long wavelength and without any additive.
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