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| 1038899-78-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1038899-78-3
化学式
C46H51N3O13
mdl
——
分子量
853.923
InChiKey
UIHZPLHBUDSZQZ-DLUHDUGVSA-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

反应信息

  • 作为反应物:
    描述:
    溶剂黄146乙二胺 作用下, 以 四氢呋喃 为溶剂, 反应 8.0h, 以64%的产率得到
    参考文献:
    名称:
    Synthesis of diglycosylceramides and evaluation of their iNKT cell stimulatory properties
    摘要:
    Stimulation of iNKT cells is highly dependent on the structures of the glycolipids presented by CD1d. Furthermore, antigen processing and CD1d loading in lysosomes play central roles in controlling the stimulatory properties of glycolipid antigens. Previously, we determined that substitution at C6 '' on alpha-galactosylceramides did not significantly impact stimulatory properties; however, it was not known if substitution at this position influenced lysosomal processing of oligoglycosylceramides. We have prepared a series of mono- and di-galactosylceramides to observe the impact of C6 '' substitution on glycosidase truncation of these glycolipids. We found that substitution did not significantly impact glycosidase activity or loading into CD1d. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.12.067
  • 作为产物:
    描述:
    2,3,4,6-四-O-苄基-D-吡喃半乳糖三氯乙亚氨酸酯三氟甲磺酸三甲基硅酯 、 4 A molecular sieve 作用下, 以 二氯甲烷 为溶剂, 反应 14.0h, 以37%的产率得到
    参考文献:
    名称:
    Synthesis of diglycosylceramides and evaluation of their iNKT cell stimulatory properties
    摘要:
    Stimulation of iNKT cells is highly dependent on the structures of the glycolipids presented by CD1d. Furthermore, antigen processing and CD1d loading in lysosomes play central roles in controlling the stimulatory properties of glycolipid antigens. Previously, we determined that substitution at C6 '' on alpha-galactosylceramides did not significantly impact stimulatory properties; however, it was not known if substitution at this position influenced lysosomal processing of oligoglycosylceramides. We have prepared a series of mono- and di-galactosylceramides to observe the impact of C6 '' substitution on glycosidase truncation of these glycolipids. We found that substitution did not significantly impact glycosidase activity or loading into CD1d. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.12.067
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