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2-amino-4-(benzyloxy)pteridin-7(8H)-one | 49560-77-2

中文名称
——
中文别名
——
英文名称
2-amino-4-(benzyloxy)pteridin-7(8H)-one
英文别名
2-amino-4-benzyloxy-8H-pteridin-7-one;2-amino-4-phenylmethoxy-8H-pteridin-7-one
2-amino-4-(benzyloxy)pteridin-7(8H)-one化学式
CAS
49560-77-2
化学式
C13H11N5O2
mdl
——
分子量
269.263
InChiKey
QPEKAMWAWRKPNZ-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

物化性质

  • 密度:
    1.53±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    103
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis of 8-(2-Deoxy-β-D-Ribofuranosyl)-Isoxanthopterins New Fluorescent Analogs of 2′-Deoxyguanosine
    摘要:
    We have synthesized isoxanthopterin and 6-phenylisoxanthopterin nucleosides in form of their 5'-O-dimethoxytritylated 3'-phosphoramidites to be used as fluorescence markers directly in the synthesis of oligonucleotides by a machine-aided solid-support approach. The preparation of the monomers and some results of the oligonucleotide synthesis will be described.
    DOI:
    10.1080/07328319708002965
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文献信息

  • Nucleotides, Part LXIX, Synthesis of Phosphoramidite Building Blocks of IsoxanthopterinN8-(2′-Deoxy-β-D-ribonucleosides): New Fluorescence Markers for Oligonucleotide Synthesis
    作者:Jörg Lehbauer、Wolfgang Pfleiderer
    DOI:10.1002/1522-2675(20010815)84:8<2330::aid-hlca2330>3.0.co;2-u
    日期:2001.8.15
    The chemical synthesis of isoxanthopterin and 6-phenylisoxanthopterin N-8-(2'-deoxy-beta -D-ribofuranosyl nucleosides) is described as well as their conversion into suitably protected 3'-phosphoramidite building blocks to be used as marker molecules for DNA synthesis. Applying the npe/npeoc (=2-(4-nitrophenyl)ethyl/[2-(4-nitrophenyl)ethoxy]carbonyl) strategy, we used the new building blocks in the preparation of oligonucleotides by an automated solid-support approach, The hybridization properties of a series of labelled oligomers were studied by UV-melting techniques. It was found that the newly synthesized markers only slightly interfered with the abilities of the labelled oligomers to form stable duplexes with complementary oligonucleotides.
  • PTERIDINE NUCLEOTIDE ANALOGS AS FLUORESCENT DNA PROBES
    申请人:THE GOVERNMENT OF THE UNITED STATES OF AMERICA as represented by the SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES
    公开号:EP0759927A1
    公开(公告)日:1997-03-05
  • Nucleosides With Non-Natural Bases as Anti-Viral Agents
    申请人:Pierra Claire
    公开号:US20100279974A1
    公开(公告)日:2010-11-04
    A method and composition for treating a host infected with flavivirus, pestivirus or hepacivirus comprising administering an effective flavivirus, pestivirus or hepacivirus treatment amount of a described base-modified nucleoside or a pharmaceutically acceptable salt or prodrug thereof, is provided.
  • US5525711A
    申请人:——
    公开号:US5525711A
    公开(公告)日:1996-06-11
  • US5612468A
    申请人:——
    公开号:US5612468A
    公开(公告)日:1997-03-18
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