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6-N-benzoyl-9-(5-O-benzoyl-3-O-benzyl-α-L-arabinofuranosyl)adenine | 525596-23-0

中文名称
——
中文别名
——
英文名称
6-N-benzoyl-9-(5-O-benzoyl-3-O-benzyl-α-L-arabinofuranosyl)adenine
英文别名
[(2S,3R,4R,5R)-5-(6-benzamidopurin-9-yl)-4-hydroxy-3-phenylmethoxyoxolan-2-yl]methyl benzoate
6-N-benzoyl-9-(5-O-benzoyl-3-O-benzyl-α-L-arabinofuranosyl)adenine化学式
CAS
525596-23-0
化学式
C31H27N5O6
mdl
——
分子量
565.585
InChiKey
KZRQILKOFWPANU-LFNVBFKESA-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):
    3.6
  • 重原子数:
    42
  • 可旋转键数:
    10
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    138
  • 氢给体数:
    2
  • 氢受体数:
    9

上下游信息

  • 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:
    参考文献:
    名称:
    Synthesis and RNA-selective hybridization of α-l-ribo- and β-d-lyxo-configured oligonucleotides
    摘要:
    Three alpha-L-ribofuranosyl analogues of RNA nucleotides (alpha-L-RNA analogues) have been synthesized and incorporated into oligonucleotides using the phosphoramide approach on an automated DNA synthesizer. The 4'-C-hydroxymethyl-alpha-L-ribofuranosyl thymine monomer was furthermore synthesized. Relative to the unmodified duplexes, incorporation of a single a-L-RNA monomer into a DNA strand leads to reduced thermal stability of duplexes with DNA complements but unchanged thermal stability of duplexes with RNA complements, whereas incorporation of more than one alpha-L-RNA monomer lead to moderately decreased thermal stability also of duplexes with RNA complements. Efficient hybridization with an RNA complement and no melting transition with a DNA complement were observed with stereoregular chimeric oligonucleotides composed of a mixture of alpha-L-RNA and affinity enhancing alpha-L-LNA monomers (alpha-L-ribo-configured locked nucleic acid). Furthermore, duplexes formed between oligodeoxynucleotides containing an alpha-L-RNA monomer and complementary RNA were good substrates for Escherichia coli RNase H. RNA-selective hybridization was also achieved by the incorporation of 1-(4-C-hydroxymethyl-beta-D-lyxofuranosyl)thymine monomers into a DNA strand, whereas stable duplexes were formed with both complementary DNA and RNA when these monomers were incorporated into an RNA strand. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2005.12.007
  • 作为产物:
    参考文献:
    名称:
    Synthesis and RNA-selective hybridization of α-l-ribo- and β-d-lyxo-configured oligonucleotides
    摘要:
    Three alpha-L-ribofuranosyl analogues of RNA nucleotides (alpha-L-RNA analogues) have been synthesized and incorporated into oligonucleotides using the phosphoramide approach on an automated DNA synthesizer. The 4'-C-hydroxymethyl-alpha-L-ribofuranosyl thymine monomer was furthermore synthesized. Relative to the unmodified duplexes, incorporation of a single a-L-RNA monomer into a DNA strand leads to reduced thermal stability of duplexes with DNA complements but unchanged thermal stability of duplexes with RNA complements, whereas incorporation of more than one alpha-L-RNA monomer lead to moderately decreased thermal stability also of duplexes with RNA complements. Efficient hybridization with an RNA complement and no melting transition with a DNA complement were observed with stereoregular chimeric oligonucleotides composed of a mixture of alpha-L-RNA and affinity enhancing alpha-L-LNA monomers (alpha-L-ribo-configured locked nucleic acid). Furthermore, duplexes formed between oligodeoxynucleotides containing an alpha-L-RNA monomer and complementary RNA were good substrates for Escherichia coli RNase H. RNA-selective hybridization was also achieved by the incorporation of 1-(4-C-hydroxymethyl-beta-D-lyxofuranosyl)thymine monomers into a DNA strand, whereas stable duplexes were formed with both complementary DNA and RNA when these monomers were incorporated into an RNA strand. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2005.12.007
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