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[6'-(4-Aminobenzoyl)oxy-4',5'-dimethyl-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl] 4-aminobenzoate | 1333505-25-1

中文名称
——
中文别名
——
英文名称
[6'-(4-Aminobenzoyl)oxy-4',5'-dimethyl-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl] 4-aminobenzoate
英文别名
[6'-(4-aminobenzoyl)oxy-4',5'-dimethyl-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl] 4-aminobenzoate
[6'-(4-Aminobenzoyl)oxy-4',5'-dimethyl-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl] 4-aminobenzoate化学式
CAS
1333505-25-1
化学式
C36H26N2O7
mdl
——
分子量
598.612
InChiKey
AJPVMVUKWQGPAD-UHFFFAOYSA-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):
    6.3
  • 重原子数:
    45
  • 可旋转键数:
    6
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    140
  • 氢给体数:
    2
  • 氢受体数:
    9

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:
    4,6-O-(1-butylidene)-D-glucopyranose 、 [6'-(4-Aminobenzoyl)oxy-4',5'-dimethyl-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl] 4-aminobenzoate甲醇 为溶剂, 反应 10.0h, 以50%的产率得到[6'-[4-[[(4aR,6R,7R,8R,8aS)-7,8-dihydroxy-2-propyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]amino]benzoyl]oxy-4',5'-dimethyl-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl] 4-[[(4aR,6R,7R,8R,8aS)-7,8-dihydroxy-2-propyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]amino]benzoate
    参考文献:
    名称:
    Design, synthesis, and biological evaluation of a novel class of fluorescein-based N-glycosylamines
    摘要:
    A series of fluorescein-based N-glycosylamines was synthesized from the corresponding fluorescein amine and a partially protected D-glucose. The physiochemical investigation of these compounds by spectral and morphological studies reveals their gelation potential. The exclusive localization of fluorescence in the cytoplasm through cell imaging studies reveals the anti-cancer potentials of N-glycosylamines. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.06.001
  • 作为产物:
    描述:
    [4',5'-Dimethyl-6'-(4-nitrobenzoyl)oxy-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl] 4-nitrobenzoate 在 palladium 10% on activated carbon 、 氢气 作用下, 以 四氢呋喃 为溶剂, 反应 25.0h, 以77%的产率得到[6'-(4-Aminobenzoyl)oxy-4',5'-dimethyl-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl] 4-aminobenzoate
    参考文献:
    名称:
    Design, synthesis, and biological evaluation of a novel class of fluorescein-based N-glycosylamines
    摘要:
    A series of fluorescein-based N-glycosylamines was synthesized from the corresponding fluorescein amine and a partially protected D-glucose. The physiochemical investigation of these compounds by spectral and morphological studies reveals their gelation potential. The exclusive localization of fluorescence in the cytoplasm through cell imaging studies reveals the anti-cancer potentials of N-glycosylamines. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2011.06.001
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文献信息

  • Design, synthesis, and biological evaluation of a novel class of fluorescein-based N-glycosylamines
    作者:Mani Rajasekar、Sulaiman Mahaboob Khan、Sivasithamparam Niranjali Devaraj、Thangamuthu Mohan Das
    DOI:10.1016/j.carres.2011.06.001
    日期:2011.9
    A series of fluorescein-based N-glycosylamines was synthesized from the corresponding fluorescein amine and a partially protected D-glucose. The physiochemical investigation of these compounds by spectral and morphological studies reveals their gelation potential. The exclusive localization of fluorescence in the cytoplasm through cell imaging studies reveals the anti-cancer potentials of N-glycosylamines. (C) 2011 Elsevier Ltd. All rights reserved.
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