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1-[(1R,2S,3R,4S)-2,3,4-trihydroxycyclopent-1-yl]-8-methylthioimidazo-[4,5-g]quinazoline | 395066-48-5

中文名称
——
中文别名
——
英文名称
1-[(1R,2S,3R,4S)-2,3,4-trihydroxycyclopent-1-yl]-8-methylthioimidazo-[4,5-g]quinazoline
英文别名
(1S,2R,3S,4R)-4-(8-methylsulfanylimidazo[4,5-g]quinazolin-1-yl)cyclopentane-1,2,3-triol
1-[(1R,2S,3R,4S)-2,3,4-trihydroxycyclopent-1-yl]-8-methylthioimidazo-[4,5-g]quinazoline化学式
CAS
395066-48-5
化学式
C15H16N4O3S
mdl
——
分子量
332.383
InChiKey
KOEQPCWPOADTJU-ZOBORPQBSA-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

  • 沸点:
    619.2±65.0 °C(Predicted)
  • 密度:
    1.74±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.1
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    130
  • 氢给体数:
    3
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    1-[(1R,2S,3R,4S)-2,3,4-trihydroxycyclopent-1-yl]-8-methylthioimidazo-[4,5-g]quinazoline盐酸 作用下, 反应 4.0h, 以67%的产率得到1-[(1R,2S,3R,4S)-2,3,4-trihydroxycyclopent-1-yl]imidazo[4,5-g]-quinazolin-8-one
    参考文献:
    名称:
    An 8-aminoimidazo[4,5-g]quinazoline carbocyclic nucleoside: a ring-extended analog of 5′-noraristeromycin
    摘要:
    The antiviral properties of 5 ' -noraristeromycin (3) have been attributed to its inhibition of S-adenosylhomocysteine hydrolase. As part of an effort to establish the limiting structural parameters possible for the biological properties of 3, a ring-extended analog possessing 8-aminoimidazo[4,5-g]quinazoline as the base (7) has been prepared and found to be less active than 3. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00909-7
  • 作为产物:
    参考文献:
    名称:
    An 8-aminoimidazo[4,5-g]quinazoline carbocyclic nucleoside: a ring-extended analog of 5′-noraristeromycin
    摘要:
    The antiviral properties of 5 ' -noraristeromycin (3) have been attributed to its inhibition of S-adenosylhomocysteine hydrolase. As part of an effort to establish the limiting structural parameters possible for the biological properties of 3, a ring-extended analog possessing 8-aminoimidazo[4,5-g]quinazoline as the base (7) has been prepared and found to be less active than 3. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(01)00909-7
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