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3-[1,3-di(tetradecyloxycarbonyl)propylcarbamoyl]propanoic acid | 125401-59-4

中文名称
——
中文别名
——
英文名称
3-[1,3-di(tetradecyloxycarbonyl)propylcarbamoyl]propanoic acid
英文别名
4-[[(2S)-1,5-dioxo-1,5-di(tetradecoxy)pentan-2-yl]amino]-4-oxobutanoic acid
3-[1,3-di(tetradecyloxycarbonyl)propylcarbamoyl]propanoic acid化学式
CAS
125401-59-4
化学式
C37H69NO7
mdl
——
分子量
639.957
InChiKey
JJZNNEBZVZZMDZ-XIFFEERXSA-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):
    9.6
  • 重原子数:
    45.0
  • 可旋转键数:
    34.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    119.0
  • 氢给体数:
    2.0
  • 氢受体数:
    6.0

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

  • 作为反应物:
    描述:
    3-[1,3-di(tetradecyloxycarbonyl)propylcarbamoyl]propanoic acid 生成 potassium;4-[[(2S)-1,5-dioxo-1,5-di(tetradecoxy)pentan-2-yl]amino]-4-oxobutanoate
    参考文献:
    名称:
    ROSENBERG, JORG;GRUNHAGEN, HANS-HEINRICH;LENKE, DIETER
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    叔胺类阳离子脂质衍生物及其在RNA药物递 送系统的应用
    摘要:
    本发明涉及化学与制剂领域,具体涉及叔胺类阳离子脂质衍生物及其在RNA药物递送系统中的应用。本发明的阳离子脂质以叔胺片段作为亲水部分,以氨基酸作为骨架,以酯键作为连接键,以烷烃结构作为疏水部分,具有生物相容性好、安全性高等优势;合成方法简便快捷,合成成本低,有利于大规模生产。基于本发明设计的阳离子脂质构建的阳离子脂质体,如A13,能稳定荷载siRNA,在多种人源肿瘤细胞上基因沉默效果优于阳性对照Lipofectamine2000,并能抵抗血清存在对基因沉默效果的影响。本发明将提供一类具有高转染效率的新型阳离子脂质,并为RNA药物递送提供安全高效的非病毒载体平台。
    公开号:
    CN109503411B
点击查看最新优质反应信息

文献信息

  • Induction of protein-like molecular architecture by self-assembly processes
    作者:Gregg B. Fields
    DOI:10.1016/s0968-0896(98)00216-8
    日期:1999.1
    potentially triple-helical structural motifs have been synthesized. The resultant head group structures have been characterized by circular dichroism and NMR spectroscopies. Evidence for a self-assembly process of peptide-amphiphiles has been obtained from: (a) circular dichroism spectra and melting curves characteristic of triple-helices, (b) one- and two-dimensional NMR spectra indicative of stable
    最有趣的自组装过程之一是将肽链折叠成天然蛋白质结构。我们已经开发出一种构建具有生物学意义的序列的蛋白样结构基序的方法。亲脂性部分连接到肽链的Nα-基上,产生“肽-两亲物”。在脂质溶剂界面处的两亲化合物的比对用于促进肽比对以及结构的起始和繁殖。已经合成了含有潜在三螺旋结构基序的肽-两亲物。所得的头基结构已通过圆二色性和NMR光谱学表征。肽两亲分子自组装过程的证据来自:(a)三重螺旋的圆二色性光谱和熔融曲线特征;(b)指示低温下稳定的三螺旋结构和高温下熔融的三重螺旋的一维和二维NMR光谱,以及(c)脉冲场梯度NMR实验证明了建议的三螺旋和非三螺旋物种之间的不同自扩散系数。本文所述的肽-两亲物提供了使用肽头基团建立稳定的蛋白质结构基序的简单方法。(c)脉冲场梯度NMR实验,证明拟议的三螺旋和非三螺旋物种之间具有不同的自扩散系数。本文所述的肽-两亲物提供了使用肽头基团构建稳定的蛋白质结构基序的简
  • Synthesis of neoglycolipids based on D-lactose
    作者:L. Yu. Gur’eva、U. A. Budanova、Yu. L. Sebyakin
    DOI:10.1134/s1070428009020031
    日期:2009.2
    A synthesis was performed of amphiphilic D-lactose derivatives differing by the length and number of aliphatic chains. The compounds may be applied to the carbohydrate modification of phosphatidylcholine liposomes.
  • Thermodynamic and structural characterization of amino acid-linked dialkyl lipids
    作者:Stephanie Tristram-Nagle、Ruthven N.A.H. Lewis、Joseph W. Blickenstaff、Michael DiPrima、Bruno F. Marques、Ronald N. McElhaney、John F. Nagle、James W. Schneider
    DOI:10.1016/j.chemphyslip.2004.11.001
    日期:2005.3
    Using differential scanning calorimetry (DSC), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FI'IR), we determined some thermodynamic and structural parameters for a series of amino acid-linked dialkyl lipids containing a glutamic acid-succinate headgroup, and di-alkyl chains: C12, C14, C16 and C18 in CHES buffer, pH 10. Upon heating, DSC shows that the C12, C14 and annealed C 16 lipids undergo a single transition which XRD shows is from a lamellar, chain ordered subgel phase to a fluid phase. This single transition splits into two transitions for C18, and FTIR shows that the upper main transition is predominantly the melting of the hydrocarbon chains whereas the lower transition involves changes in the headgroup ordering as well as changes in the lateral packing of the chains. For short incubation times at low temperature, the C 16 lipid appears to behave like the C18 lipid, but appropriate annealing at low temperatures indicates that its true equilibrium behavior is like the shorter chain lipids. XRD shows that the C12 lipid readily converts into a highly ordered subgel phase upon cooling and suggests a model with untilted, interdigitated chains and an area of 77.2 angstrom(2)/4 chains, with a distorted orthorhombic unit subcell, a = 9.0 angstrom, b = 4.3 angstrom and beta = 92.7 degrees. As the chain length n increases, subgel formation is slowed, but untilted, interdigitated chains prevail. (c) 2004 Elsevier Ireland Ltd. All rights reserved.
  • Preparation of gemini-type amphiphiles bearing cyclitol head groups and their application as high-performance modifiers for lipases
    作者:Yurie Mine、Kimitoshi Fukunaga、Ken-ichi Samejima、Makoto Yoshimoto、Katsumi Nakao、Yoshiaki Sugimura
    DOI:10.1016/j.carres.2003.12.006
    日期:2004.2
    Five gemini-type amphiphiles bearing cyclitol head groups, which have abundance of axial hydroxy groups, are newly synthesized. The syntheses are based on a common mixed anhydride method utilizing N,N'-[iminobis(trimethylene)]bisquinamide, prepared from iminobispropylamine and quino-1,5-lactone, and dialkyl N-(3-carboxypropanoyl)-L-glutamates as polar and hydrophobic components, respectively. Candida rugosa lipase (CRL) and Pseudomonas cepacia lipase (PCL) are co-lyophilized with these synthesized gemini-type amphiphiles, and their transesterification activities in organic solvents are evaluated. The modified PCL and CRL prepared by using each amphiphile showed highly enhanced and moderately enhanced enzyme activity, respectively. These results are discussed in terms of the increased preferential exclusion of the hydrophilic heads of the amphiphile and of the topological view of the amphiphile. (C) 2003 Elsevier Ltd. All rights reserved.
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