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3,3'-O-(1,16-hexadecamethylene)-2,2'-di-O-<(R)-3,7-dimethyloctyl>-1-O-(2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl)-1'-O-benzyl-sn-diglycerol | 222984-24-9

中文名称
——
中文别名
——
英文名称
3,3'-O-(1,16-hexadecamethylene)-2,2'-di-O-<(R)-3,7-dimethyloctyl>-1-O-(2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl)-1'-O-benzyl-sn-diglycerol
英文别名
——
3,3'-O-(1,16-hexadecamethylene)-2,2'-di-O-<(R)-3,7-dimethyloctyl>-1-O-(2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl)-1'-O-benzyl-sn-diglycerol化学式
CAS
222984-24-9
化学式
C63H110O15
mdl
——
分子量
1107.56
InChiKey
UZMFUFVTGPSYEW-LRAZTZPGSA-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):
    13.27
  • 重原子数:
    78.0
  • 可旋转键数:
    50.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.84
  • 拓扑面积:
    169.81
  • 氢给体数:
    0.0
  • 氢受体数:
    15.0

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

点击查看最新优质反应信息

文献信息

  • An efficient synthesis of analogues of unsymmetrical archaeal tetraether glycolipids
    作者:Grégory Lecollinet、Rachel Auzély-Velty、Thierry Benvegnu、Daniel Plusquellec、Grégory Lecollinet、Grahame Mackenzie、John W. Goodby
    DOI:10.1039/a802338g
    日期:——
    Unsymmetrical tetraether analogues of glycolipids found in archaebacteria, possessing either two different carbohydrate units or a saccharidic moiety and a phosphate group as polar heads and a quasi-macrocyclic lipid core, are efficiently synthesized from versatile chiral building blocks.
    不对称的四醚类类脂质模拟物在古菌中被发现,具有两种不同的碳水化合物单元或一个糖基部分和一个磷酸基团作为极性头部,并且具有类大环脂质核心,这些化合物可以高效地从多功能的手性构建块合成。
  • Supramolecular Self-Assembling Properties of Membrane-Spanning Archaeal Tetraether Glycolipid Analogues
    作者:Grégory Lecollinet、Annette Gulik、Grahame Mackenzie、John W. Goodby、Thierry Benvegnu、Daniel Plusquellec
    DOI:10.1002/1521-3765(20020201)8:3<585::aid-chem585>3.0.co;2-5
    日期:2002.2.1
    The self-assembling properties of a new series of archaeal tetraether glycolipid analogues 1 -6 that are characterized by a bipolar architecture with two similar or different gylycosidic and/or phosphate polar heads and a lipid core possessing a cyclopentane unit and/or branched chains were studied by means of differential scanning calorimetry, optical microscopy, X-ray scattering, freeze-fracture electron microscopy and dynamic light scattering. Unsymmetrical phosphate derivatives 1 and 2 spontaneously formed thermostable multilamellar and unilamellar vesicles in which most of the bipolar lipids adopted a trans-membrane conformation, as revealed by freeze-fracture electron microscopy. Supramolecular aggregates of neutral glycolipids 3-6 were found to depend on both the saccharidic polar heads and the chain composition. The presence of one glycosidic residue with rather marked hydrophilic properties, such as the lactosyl moiety, was required to allow the formation of multilamellar vesicles. Surprisingly, the introduction of a cyclopentane unit in the bridging chain was able to induce an apparent two-by-two membrane association: this unusual behaviour might be the result of unsymmetrical interfacial properties of the lipid layer caused by the presence of the cyclopentane unit.
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