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2-azido-3,4-O-isopropylidene-D-ribo-1,3,4-hexanetriol | 745041-59-2

中文名称
——
中文别名
——
英文名称
2-azido-3,4-O-isopropylidene-D-ribo-1,3,4-hexanetriol
英文别名
(2S)-2-azido-2-[(4S,5R)-5-ethyl-2,2-dimethyl-1,3-dioxolan-4-yl]ethanol
2-azido-3,4-O-isopropylidene-D-ribo-1,3,4-hexanetriol化学式
CAS
745041-59-2
化学式
C9H17N3O3
mdl
——
分子量
215.252
InChiKey
LBBKHGDVGJETJW-RNJXMRFFSA-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):
    1.7
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    53
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    2-azido-3,4-O-isopropylidene-D-ribo-1,3,4-hexanetriol 在 Lindlar's catalyst 四丁基溴化铵氢气 作用下, 以 乙醇N,N-二甲基甲酰胺甲苯 为溶剂, 生成
    参考文献:
    名称:
    Minimum structure requirement of immunomodulatory glycolipids for predominant Th2 cytokine induction and the discovery of non-linear phytosphingosine analogs
    摘要:
    Analogs of immunomodulatory glycolipid OCH (2) were prepared and minimum structure requirement to exhibit equivalent profiles was disclosed. Analogs bearing non-linear hydrocarbon chain in the phytosphingosine moiety (18, 19) were shown for the first time to possess comparable cytokine inducing profile to 2. Molecular modeling of 2/hCD1d complex based on the crystal structure of alpha-GalCer (1)/hCDld complex is also described. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.02.081
  • 作为产物:
    描述:
    4,5-anhydro-1,3-O-benzylidene-D-arabitol 在 吡啶copper(l) iodide 、 sodium azide 、 对甲苯磺酸 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 生成 2-azido-3,4-O-isopropylidene-D-ribo-1,3,4-hexanetriol
    参考文献:
    名称:
    Minimum structure requirement of immunomodulatory glycolipids for predominant Th2 cytokine induction and the discovery of non-linear phytosphingosine analogs
    摘要:
    Analogs of immunomodulatory glycolipid OCH (2) were prepared and minimum structure requirement to exhibit equivalent profiles was disclosed. Analogs bearing non-linear hydrocarbon chain in the phytosphingosine moiety (18, 19) were shown for the first time to possess comparable cytokine inducing profile to 2. Molecular modeling of 2/hCD1d complex based on the crystal structure of alpha-GalCer (1)/hCDld complex is also described. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.02.081
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文献信息

  • Alpha-GLYCOSYL THIOLS AND alpha-S-LINKED GLYCOLIPIDS
    申请人:Zhu Xiangming
    公开号:US20100184711A1
    公开(公告)日:2010-07-22
    The present invention relates to stereoselective methods for the preparation of α-glycosyl thiols and α-S-linked glycosylceramides.
    本发明涉及用于制备α-糖基硫醇和α-S-链接糖基酰胺的立体选择性方法。
  • Glycolipid derivatives, process for production of the same, intermediates for synthesis thereof, and process for production of the intermediates
    申请人:Japan as represented by President of National Center of Neurology and Psychiatry Ministry of Health
    公开号:EP2343306A1
    公开(公告)日:2011-07-13
    Novel glycolipid derivatives, where the substituent of the sphingosine base part is a short carbon chain alkyl group, substituted or unsubstituted cycloalkyl group, substituted or unsubstituted aryl group or substituted or unsubstituted aralkyl group and efficient synthetic methods for practical mass production of the same and intermediates useful for the synthesis of these compounds. Glycolipids having the formula (I): where R3 indicates a substituted or unsubstituted C1 to C7 linear alkyl group, substituted or unsubstituted cycloalkyl group, substituted or unsubstituted aryl group, or substituted or unsubstituted aralkyl group and R8 indicates a substituted or unsubstituted C1 to C35 alkyl group, substituted or unsubstituted aryl group or substituted or unsubstituted aralkyl group are chemically synthesized.
    新型糖脂衍生物(其中鞘磷脂基部分的取代基为短碳链烷基、取代或未取代的环烷基、取代或未取代的芳基或取代或未取代的芳烷基)以及用于实际大规模生产这些衍生物的高效合成方法和用于合成这些化合物的中间体。 具有式 (I) 的糖脂: 其中 R3 表示取代或未取代的 C1 至 C7 直链烷基、取代或未取代的环烷基、取代或未取代的芳基或取代或未取代的芳烷基,R8 表示取代或未取代的 C1 至 C35 烷基、取代或未取代的芳基或取代或未取代的芳烷基。
  • NEW GLYCOLIPIDS AND SYNTHETIC METHOD THEREOF AS WELL AS THEIR SYNTHETIC INTERMEDIATES, AND SYNTHETIC METHOD THEREOF
    申请人:ANNOURA Hirokazu
    公开号:US20100210828A1
    公开(公告)日:2010-08-19
    Novel glycolipid derivatives, where the substituent of the sphingosine base part is a short carbon chain alkyl group, substituted or unsubstituted cycloalkyl group, substituted or unsubstituted aryl group or substituted or unsubstituted aralkyl group and efficient synthetic methods for practical mass production of the same and intermediates useful for the synthesis of these compounds. Glycolipids having the formula (I): where R 3 indicates a substituted or unsubstituted C 1 to C 7 linear alkyl group, substituted or unsubstituted cycloalkyl group, substituted or unsubstituted aryl group, or substituted or unsubstituted aralkyl group and R 8 indicates a substituted or unsubstituted C 1 to C 35 alkyl group, substituted or unsubstituted aryl group or substituted or unsubstituted aralkyl group are chemically synthesized.
  • US7732583B2
    申请人:——
    公开号:US7732583B2
    公开(公告)日:2010-06-08
  • US8034908B2
    申请人:——
    公开号:US8034908B2
    公开(公告)日:2011-10-11
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