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3',5'-di-O-acetyl-5-[1-(1H,1H,2H,2H-perfluorooctyl)-1H-1,2,3-triazol-4-yl]-2'-deoxyuridine | 1254757-25-9

中文名称
——
中文别名
——
英文名称
3',5'-di-O-acetyl-5-[1-(1H,1H,2H,2H-perfluorooctyl)-1H-1,2,3-triazol-4-yl]-2'-deoxyuridine
英文别名
[(2R,3S,5R)-3-acetyloxy-5-[2,4-dioxo-5-[1-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)triazol-4-yl]pyrimidin-1-yl]oxolan-2-yl]methyl acetate
3',5'-di-O-acetyl-5-[1-(1H,1H,2H,2H-perfluorooctyl)-1H-1,2,3-triazol-4-yl]-2'-deoxyuridine化学式
CAS
1254757-25-9
化学式
C23H20F13N5O7
mdl
——
分子量
725.42
InChiKey
CKECMNAYJJEGGB-RRFJBIMHSA-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):
    3.5
  • 重原子数:
    48
  • 可旋转键数:
    14
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.65
  • 拓扑面积:
    142
  • 氢给体数:
    1
  • 氢受体数:
    22

反应信息

  • 作为反应物:
    描述:
    3',5'-di-O-acetyl-5-[1-(1H,1H,2H,2H-perfluorooctyl)-1H-1,2,3-triazol-4-yl]-2'-deoxyuridine 、 lithium hydroxide 作用下, 以 甲醇 为溶剂, 生成 5-[1-(1H,1H,2H,2H-perfluorooctyl)-1H-1,2,3-triazol-4-yl]-2'-deoxyuridine
    参考文献:
    名称:
    Design, synthesis, and anticancer activities of novel perfluoroalkyltriazole-appended 2′-deoxyuridines
    摘要:
    We have focused on the C5-modification of 2'-deoxyuridine with substituted heterocycles for bioactivity, such as antiviral or anticancer activity. Herein, we report a novel class of nucleoside analogues with perfluoroalkyltriazole moiety as an anticancer drug candidate. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.07.126
  • 作为产物:
    描述:
    8-azido-1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorooctane 、 5-ethynyl-2'-deoxyuridine 在 copper diacetate 、 sodium ascorbate 作用下, 以 二氯甲烷 为溶剂, 以87%的产率得到3',5'-di-O-acetyl-5-[1-(1H,1H,2H,2H-perfluorooctyl)-1H-1,2,3-triazol-4-yl]-2'-deoxyuridine
    参考文献:
    名称:
    Design, synthesis, and anticancer activities of novel perfluoroalkyltriazole-appended 2′-deoxyuridines
    摘要:
    We have focused on the C5-modification of 2'-deoxyuridine with substituted heterocycles for bioactivity, such as antiviral or anticancer activity. Herein, we report a novel class of nucleoside analogues with perfluoroalkyltriazole moiety as an anticancer drug candidate. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.07.126
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文献信息

  • Design, synthesis, and anticancer activities of novel perfluoroalkyltriazole-appended 2′-deoxyuridines
    作者:Sun Min Park、Heeju Yang、Song-Kyu Park、Hwan Mook Kim、Byeang Hyean Kim
    DOI:10.1016/j.bmcl.2010.07.126
    日期:2010.10
    We have focused on the C5-modification of 2'-deoxyuridine with substituted heterocycles for bioactivity, such as antiviral or anticancer activity. Herein, we report a novel class of nucleoside analogues with perfluoroalkyltriazole moiety as an anticancer drug candidate. (C) 2010 Elsevier Ltd. All rights reserved.
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