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| 1045703-67-0

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1045703-67-0
化学式
C61H63BrO10
mdl
——
分子量
1036.07
InChiKey
JWVSSRFCWPYAHB-QURBWNRWSA-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:
    6-O-[2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl]-3,4,5-tri-O-benzyl-1-O-[(2-cyanoethyloxy)-(2-O-benzyloxycarbonyl-3-O-octadecyl-sn-glycerol)phosphono]-2-O-palmitoleoyl-myo-inositol 、 silver trifluoromethanesulfonate 作用下, 以 二氯甲烷甲苯 为溶剂, 反应 0.5h, 生成
    参考文献:
    名称:
    Synthesis and biological evaluation of sperm CD52 GPI anchor and related derivatives as binding receptors of pore-forming CAMP factor
    摘要:
    Sperm CD52 GPI anchor and its derivatives containing different carbohydrate chains were prepared, in a highly convergent fashion starting from the same properly protected phospholipidated pseudodisaccharide. Coupling this common key intermediate to various oligosaccharyl donors quickly afforded the framework of the synthetic targets, which was followed by global deprotection to furnish the desired structures. Preliminary studies on the biological properties of the synthetic GPI derivatives indicated that both the intact GPI anchor and the free phospholipidated pseudodisaccharide interacted strongly with CAMP factor, a pore-forming bacterial toxin. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2008.03.033
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