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1-O-benzyl-2-N-tert-butoxycarbonyl-4,6-di-O-tert-butyldimethylsilyl-2-N,3-O-carbonyl-α-L-sorbofuranosylamine | 575472-11-6

中文名称
——
中文别名
——
英文名称
1-O-benzyl-2-N-tert-butoxycarbonyl-4,6-di-O-tert-butyldimethylsilyl-2-N,3-O-carbonyl-α-L-sorbofuranosylamine
英文别名
tert-butyl (3aR,5S,6R,6aS)-6-[tert-butyl(dimethyl)silyl]oxy-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-2-oxo-3a-(phenylmethoxymethyl)-6,6a-dihydro-5H-furo[2,3-d][1,3]oxazole-3-carboxylate
1-O-benzyl-2-N-tert-butoxycarbonyl-4,6-di-O-tert-butyldimethylsilyl-2-N,3-O-carbonyl-α-L-sorbofuranosylamine化学式
CAS
575472-11-6
化学式
C31H53NO8Si2
mdl
——
分子量
623.935
InChiKey
XMKUZKRXBOXZQS-TXHDDHBJSA-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):
    7.47
  • 重原子数:
    42
  • 可旋转键数:
    13
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.74
  • 拓扑面积:
    92.8
  • 氢给体数:
    0
  • 氢受体数:
    8

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-benzyl-2-N-tert-butoxycarbonyl-4,6-di-O-tert-butyldimethylsilyl-2-N,3-O-carbonyl-α-L-sorbofuranosylamine 在 palladium on activated charcoal 氢气三氟乙酸 作用下, 以 甲醇 为溶剂, 生成 2-N,3-O-carbonyl-α-L-sorbofuranosylamine
    参考文献:
    名称:
    Inhibition of the d-fructose transporter protein GLUT5 by fused-ring glyco-1,3-oxazolidin-2-thiones and -oxazolidin-2-ones
    摘要:
    The glucose transporter 5 (GLUT5)-a specific D-fructose transporter-belongs to a family of facilitating sugar transporters recently enlarged by the human genome sequencing. Prompted by the need to develop specific photolabels of these isoforms, we have studied the interaction of conformationally locked D-fructose and L-sorbose derived 1,3-oxazolidin-2-thiones and 1,3-oxazolidin-2-ones to provide a rational basis for an interaction model. The inhibition properties of the D-fructose transporter GLUT5 by glyco-1,3-oxazolidin-2-thiones and glyco-1,3-oxazolidin-2-ones is now reported. In vitro, the fused-rings systems tested showed an efficient inhibition of GLUT5, thus bringing new insights on the interaction of D-fructose with GLUT5. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(03)00007-7
  • 作为产物:
    参考文献:
    名称:
    Inhibition of the d-fructose transporter protein GLUT5 by fused-ring glyco-1,3-oxazolidin-2-thiones and -oxazolidin-2-ones
    摘要:
    The glucose transporter 5 (GLUT5)-a specific D-fructose transporter-belongs to a family of facilitating sugar transporters recently enlarged by the human genome sequencing. Prompted by the need to develop specific photolabels of these isoforms, we have studied the interaction of conformationally locked D-fructose and L-sorbose derived 1,3-oxazolidin-2-thiones and 1,3-oxazolidin-2-ones to provide a rational basis for an interaction model. The inhibition properties of the D-fructose transporter GLUT5 by glyco-1,3-oxazolidin-2-thiones and glyco-1,3-oxazolidin-2-ones is now reported. In vitro, the fused-rings systems tested showed an efficient inhibition of GLUT5, thus bringing new insights on the interaction of D-fructose with GLUT5. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(03)00007-7
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文献信息

  • Inhibition of the d-fructose transporter protein GLUT5 by fused-ring glyco-1,3-oxazolidin-2-thiones and -oxazolidin-2-ones
    作者:Jolanta Girniene、Arnaud Tatibouët、Algirdas Sackus、Jing Yang、Geoffrey D Holman、Patrick Rollin
    DOI:10.1016/s0008-6215(03)00007-7
    日期:2003.4
    The glucose transporter 5 (GLUT5)-a specific D-fructose transporter-belongs to a family of facilitating sugar transporters recently enlarged by the human genome sequencing. Prompted by the need to develop specific photolabels of these isoforms, we have studied the interaction of conformationally locked D-fructose and L-sorbose derived 1,3-oxazolidin-2-thiones and 1,3-oxazolidin-2-ones to provide a rational basis for an interaction model. The inhibition properties of the D-fructose transporter GLUT5 by glyco-1,3-oxazolidin-2-thiones and glyco-1,3-oxazolidin-2-ones is now reported. In vitro, the fused-rings systems tested showed an efficient inhibition of GLUT5, thus bringing new insights on the interaction of D-fructose with GLUT5. (C) 2003 Elsevier Science Ltd. All rights reserved.
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