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N4-oleoy-N9-stearoyl spermine | 1380676-86-7

中文名称
——
中文别名
——
英文名称
N4-oleoy-N9-stearoyl spermine
英文别名
N4-oleoyl-N9-stearoyl-1,12-diamino-4,9-diazadodecane;N4-oleoy-N9-stearoyl-1,12-diamino-4,9-diazadodecane
N4-oleoy-N9-stearoyl spermine化学式
CAS
1380676-86-7
化学式
C46H92N4O2
mdl
——
分子量
733.262
InChiKey
YENKPJHCISVXCP-ZPHPHTNESA-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):
    12.42
  • 重原子数:
    52.0
  • 可旋转键数:
    42.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    92.66
  • 氢给体数:
    2.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    参考文献:
    名称:
    Efficient Silencing of EGFP Reporter Gene with siRNA Delivered by Asymmetrical N4,N9-Diacyl Spermines
    摘要:
    It is important to obtain structure-activity relationship (SAR) data across cationic lipids for the self-assembly and nonviral intracellular delivery of siRNA. The aims of this work are to carry out a SAR study on the efficiency of asymmetrical N-4,N-9-diacyl spermines in siRNA delivery and EGFP reporter gene silencing, with comparisons to selected mixtures composed of symmetrical N-4,N-9-diacyl spermines. Another important aim of these studies is to quantify the changes in cell viability, assayed with alamarBlue, as a function of lipid structure. Therefore, we have designed, synthesized, purified, and assayed novel cationic lipids that are asymmetrical lipopolyamines based on spermine. Flow cytometry and fluorescence microscopy in an EGFP stably transfected HeLa cell line, measuring both delivery of fluorescently tagged siRNAs and silencing the EGFP signal, allowed quantitation of the differences between asymmetrical cationic lipids, mixtures of their symmetrical counterparts, and comparison with commercial nonviral delivery agents. Intracellular delivery of siRNA and gene silencing by siRNA differ with different hydrophobic domains. In these asymmetrical N-4,N-9-diacyl spermines, lipids that enhance siRNA uptake do not necessarily enhance siRNA-induced inhibition of gene expression: C18 and longer saturated chains promote uptake, while more unsaturated C18 chains promote gene silencing. These properties are efficiently demonstrated in a new nontoxic cationic lipid siRNA vector, N-4-linoleoyl-N-9-oleoyl-1,12-diamino-4,9-diazadodecane (LinOS), which is also shown to be comparable with or superior to TransIT-TKO and Lipofectamine 2000.
    DOI:
    10.1021/mp200429n
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