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1-O-(2,3,4-tri-O-benzyl-6-deoxy-6-[N-(5-dimethylaminonaphth-1-ylsulfonyl)amido]-α-D-galactopyranosyl)-2-hexacosanoylamino-D-ribo-octadecane-1,3,4-triol | 1309598-32-0

中文名称
——
中文别名
——
英文名称
1-O-(2,3,4-tri-O-benzyl-6-deoxy-6-[N-(5-dimethylaminonaphth-1-ylsulfonyl)amido]-α-D-galactopyranosyl)-2-hexacosanoylamino-D-ribo-octadecane-1,3,4-triol
英文别名
N-[(2S,3S,4R)-1-[(2S,3R,4S,5S,6R)-6-[[[5-(dimethylamino)naphthalen-1-yl]sulfonylamino]methyl]-3,4,5-tris(phenylmethoxy)oxan-2-yl]oxy-3,4-dihydroxyoctadecan-2-yl]hexacosanamide
1-O-(2,3,4-tri-O-benzyl-6-deoxy-6-[N-(5-dimethylaminonaphth-1-ylsulfonyl)amido]-α-D-galactopyranosyl)-2-hexacosanoylamino-D-ribo-octadecane-1,3,4-triol化学式
CAS
1309598-32-0
化学式
C83H129N3O10S
mdl
——
分子量
1361.02
InChiKey
IATAVAASHPLQTK-NYBHSFFDSA-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):
    24.3
  • 重原子数:
    97
  • 可旋转键数:
    57
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    174
  • 氢给体数:
    4
  • 氢受体数:
    12

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
  • 下游产品
    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:
    1-O-(2,3,4-tri-O-benzyl-6-deoxy-6-[N-(5-dimethylaminonaphth-1-ylsulfonyl)amido]-α-D-galactopyranosyl)-2-hexacosanoylamino-D-ribo-octadecane-1,3,4-triol 在 20 % Pd(OH)2/C 、 氢气 作用下, 以 乙醇氯仿 为溶剂, 反应 17.0h, 以62%的产率得到(2S,3S,4R)-1-O-(6-deoxy-6[N-(5-[dimethylamino]naphth-1-ylsulfonyl)amino]-α-d-galactopyranosyl)-2-(hexacosanoyl)amino-octadecan-1,3,4-triol
    参考文献:
    名称:
    An improved synthesis of dansylated α-galactosylceramide and its use as a fluorescent probe for the monitoring of glycolipid uptake by cells
    摘要:
    A highly efficient synthesis of the biologically important fluorescent probe dansyl alpha-GalCer is presented. Key in our strategy is the incorporation of the fluorescent dansyl group at an early stage in the synthesis to facilitate in the monitoring and purification of intermediates via TLC and flash column chromatography, respectively, and the use of a high yielding alpha-selective glycosylation reaction between the phytosphingosine lipid and a galactosyl iodide donor. The ability of dansyl alpha-GalCer to activate iNKT cells and to serve as a fluorescent marker for the uptake of glycolipid by dendritic cells is also presented. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.02.014
  • 作为产物:
    描述:
    1-O-(2,3,4-tri-O-benzyl-6-deoxy-6-[N-(5-dimethylaminonaphth-1-ylsulfonyl)amido]-α-D-galactopyranosyl)-2-hexacosanoylamino-3,4-O-isopropylidene-D-ribo-octadecane-1,3,4-triol溶剂黄146 作用下, 以 甲苯 为溶剂, 以74%的产率得到1-O-(2,3,4-tri-O-benzyl-6-deoxy-6-[N-(5-dimethylaminonaphth-1-ylsulfonyl)amido]-α-D-galactopyranosyl)-2-hexacosanoylamino-D-ribo-octadecane-1,3,4-triol
    参考文献:
    名称:
    An improved synthesis of dansylated α-galactosylceramide and its use as a fluorescent probe for the monitoring of glycolipid uptake by cells
    摘要:
    A highly efficient synthesis of the biologically important fluorescent probe dansyl alpha-GalCer is presented. Key in our strategy is the incorporation of the fluorescent dansyl group at an early stage in the synthesis to facilitate in the monitoring and purification of intermediates via TLC and flash column chromatography, respectively, and the use of a high yielding alpha-selective glycosylation reaction between the phytosphingosine lipid and a galactosyl iodide donor. The ability of dansyl alpha-GalCer to activate iNKT cells and to serve as a fluorescent marker for the uptake of glycolipid by dendritic cells is also presented. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.02.014
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文献信息

  • An improved synthesis of dansylated α-galactosylceramide and its use as a fluorescent probe for the monitoring of glycolipid uptake by cells
    作者:Janice M.H. Cheng、Stephanie H. Chee、Deborah A. Knight、Hans Acha-Orbea、Ian F. Hermans、Mattie S.M. Timmer、Bridget L. Stocker
    DOI:10.1016/j.carres.2011.02.014
    日期:2011.5
    A highly efficient synthesis of the biologically important fluorescent probe dansyl alpha-GalCer is presented. Key in our strategy is the incorporation of the fluorescent dansyl group at an early stage in the synthesis to facilitate in the monitoring and purification of intermediates via TLC and flash column chromatography, respectively, and the use of a high yielding alpha-selective glycosylation reaction between the phytosphingosine lipid and a galactosyl iodide donor. The ability of dansyl alpha-GalCer to activate iNKT cells and to serve as a fluorescent marker for the uptake of glycolipid by dendritic cells is also presented. (C) 2011 Elsevier Ltd. All rights reserved.
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