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N-[4',6'-dioxo-2'-thioxo-1H-pyrimidin-1-yl]-6-imino-5α-cholestane | 1443436-90-5

中文名称
——
中文别名
——
英文名称
N-[4',6'-dioxo-2'-thioxo-1H-pyrimidin-1-yl]-6-imino-5α-cholestane
英文别名
——
N-[4',6'-dioxo-2'-thioxo-1H-pyrimidin-1-yl]-6-imino-5α-cholestane化学式
CAS
1443436-90-5
化学式
C31H49N3O2S
mdl
——
分子量
527.815
InChiKey
WGDVKCXHWZBRBF-MJCRIDALSA-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):
    7.1
  • 重原子数:
    37.0
  • 可旋转键数:
    6.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.87
  • 拓扑面积:
    61.77
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    5α-cholestan-6-one thiosemicarbazone丙二酸二乙酯1,4-二氧六环 为溶剂, 以70%的产率得到N-[4',6'-dioxo-2'-thioxo-1H-pyrimidin-1-yl]-6-imino-5α-cholestane
    参考文献:
    名称:
    Steroidal pyrimidines: Synthesis, characterization, molecular docking studies with DNA and in vitro cytotoxicity
    摘要:
    A series of new steroid pyrimidines (7-9) were synthesized by reacting steroidal thiosemicarbazones (46) with diethyl malonate. The new compounds were characterized by IR, H-1 NMR, C-13 NMR, MS and analytical data. The interaction studies of compounds (7-9) with DNA were carried out by employing gel electrophoresis, UV-vis and fluorescence spectroscopy. The acting force between the compounds (7-9) and DNA was mainly hydrophobic while the other interactions like van der Waals, hydrogen bonding cannot be ruled out. The gel electrophoresis pattern also demonstrated that the compound 7 alone or in presence of Cu (II) causes the nicking of supercoiled pBR322 and it seems to follow the mechanistic pathway involving generation of hydroxyl radicals that are responsible for initiating DNA strand scission. The docking study of compounds (7-9) suggested that the intercalation of compounds in between the nucleotide base pairs might be due to the presence of pyrimidine moiety in steroid molecule. MTT assay was carried out to check the toxicity of new compounds (7-9) against the different human cancer as well as non-cancer cell lines A545, MCF-7, HeLa, HL-60, SW480, HepG2, HT-29, A549, 184B5, MCF10A, NL-20, HPC and HPLF. Apoptotic degradation of DNA in presence of steroidal pyrimidines (7-9) was analyzed by agarose gel electrophoresis and visualized by ethidium bromide staining (comet assay). (C) 2013 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.molstruc.2013.04.033
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同类化合物

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