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| 1237746-99-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1237746-99-4
化学式
C59H77N3O8
mdl
——
分子量
956.276
InChiKey
IHEGIRZMHPTEBX-SIFZALJNSA-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):
    13.42
  • 重原子数:
    70.0
  • 可旋转键数:
    35.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.49
  • 拓扑面积:
    133.6
  • 氢给体数:
    1.0
  • 氢受体数:
    9.0

反应信息

  • 作为反应物:
    描述:
    氢气 、 palladium(II) hydroxide 作用下, 以 甲醇氯仿 为溶剂, 以57%的产率得到(2S,3R,4S,5S,6R)-2-(((2S,3S,4R)-2-amino-3,4-dihydroxyoctadecyl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
    参考文献:
    名称:
    Synthesis and biological activity of α-glucosyl C24:0 and C20:2 ceramides
    摘要:
    alpha-Glucosyl ceramides 4 and 5 have been synthesised and evaluated for their ability to stimulate the activation and expansion of human iNKT cells. The key challenge in the synthesis of both target molecules was the stereoselective synthesis of the alpha-glycosidic linkage. Of the methods examined, glycosylation using per-TMS-protected glucosyl iodide 16 was completely alpha-selective and provided gram quantities of amine 11, from which alpha-glucosyl ceramides 4 and 5 were obtained by N-acylation. alpha-GlcCer 4, containing a C24 saturated acyl chain, stimulated a marked proliferation and expansion of human circulating iNKT cells in short-term cultures. alpha-GlcCer 5, which contains a C20 11,14-cis-diene acyl chain (C20: 2), induced extremely similar levels of iNKT cell activation and expansion. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.05.010
  • 作为产物:
    描述:
    C63H87N3O8SSi 在 N-碘代丁二酰亚胺盐酸 作用下, 以 硝基甲烷 为溶剂, 反应 4.17h, 以47%的产率得到
    参考文献:
    名称:
    Synthesis and biological activity of α-glucosyl C24:0 and C20:2 ceramides
    摘要:
    alpha-Glucosyl ceramides 4 and 5 have been synthesised and evaluated for their ability to stimulate the activation and expansion of human iNKT cells. The key challenge in the synthesis of both target molecules was the stereoselective synthesis of the alpha-glycosidic linkage. Of the methods examined, glycosylation using per-TMS-protected glucosyl iodide 16 was completely alpha-selective and provided gram quantities of amine 11, from which alpha-glucosyl ceramides 4 and 5 were obtained by N-acylation. alpha-GlcCer 4, containing a C24 saturated acyl chain, stimulated a marked proliferation and expansion of human circulating iNKT cells in short-term cultures. alpha-GlcCer 5, which contains a C20 11,14-cis-diene acyl chain (C20: 2), induced extremely similar levels of iNKT cell activation and expansion. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.05.010
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