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Benzoic acid (2R,4S,5S)-5-(6-amino-purin-9-yl)-4-hydroxy-tetrahydro-furan-2-ylmethyl ester | 201287-87-8

中文名称
——
中文别名
——
英文名称
Benzoic acid (2R,4S,5S)-5-(6-amino-purin-9-yl)-4-hydroxy-tetrahydro-furan-2-ylmethyl ester
英文别名
——
Benzoic acid (2R,4S,5S)-5-(6-amino-purin-9-yl)-4-hydroxy-tetrahydro-furan-2-ylmethyl ester化学式
CAS
201287-87-8
化学式
C17H17N5O4
mdl
——
分子量
355.353
InChiKey
UNCVIAJTWYBKGK-WQGACYEGSA-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):
    0.91
  • 重原子数:
    26.0
  • 可旋转键数:
    4.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    125.38
  • 氢给体数:
    2.0
  • 氢受体数:
    9.0

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:
    New Unnatural L-Nucleoside Enantiomers:From Their Stereospecific Synthesis to Their Biological Activities
    摘要:
    Several purine and pyrimidine beta-L-dideoxynucleosides were stereospecifically synthesized and their antiviral properties examined. Two of them, namely beta-L-2', 3'-dideoxyadenosine (beta-L-ddA) and its 2',3'-didehydro derivative (beta-L-d4A) were found to have significant anti-human immunodeficiency virus (HIV) and anti-hepatitis B virus (HBV) activities in cell culture.
    DOI:
    10.1080/07328319708006190
  • 作为产物:
    描述:
    [(2R,4S,5S)-4-acetyloxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methyl benzoatesodium methylate 作用下, 以 四氢呋喃 为溶剂, 以40%的产率得到Benzoic acid (2R,4S,5S)-5-(6-amino-purin-9-yl)-4-hydroxy-tetrahydro-furan-2-ylmethyl ester
    参考文献:
    名称:
    Anti-human immunodeficiency and anti-hepatitis B virus activities of β-l-2′,3′-dideoxy purine nucleosides
    摘要:
    beta-L-2',3'-Dideoxyadenosine, beta-L-2',3'-didehydro-2',3'-dideoxyadenosine and related compounds were synthesized in a stereoselective manner. These compounds were tested in vitro against HBV in 2.2.15 cell line and against HIV-1 in PBM and CEM cells. It was found that beta-L-2',3'-didehydro-2',3'-dideoxyadenosine (7) exhibited significant anti-HIV (EC(50) 0.38 mu M in PBM cells) and anti-HBV activity (EC(50) 1.2 mu M). Copyright (C) 1996 Elsevier Science Ltd
    DOI:
    10.1016/0960-894x(96)00293-4
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