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N2-n-hexyl-2'-deoxyguanosine | 123994-86-5

中文名称
——
中文别名
——
英文名称
N2-n-hexyl-2'-deoxyguanosine
英文别名
——
N<sup>2</sup>-n-hexyl-2'-deoxyguanosine化学式
CAS
123994-86-5
化学式
C16H25N5O4
mdl
——
分子量
351.406
InChiKey
YRFCNNWEMPTGEQ-QJPTWQEYSA-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):
    0.75
  • 重原子数:
    25.0
  • 可旋转键数:
    8.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    125.29
  • 氢给体数:
    4.0
  • 氢受体数:
    8.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    正己胺2-溴-2'-脱氧肌苷乙醇 为溶剂, 反应 18.0h, 以58%的产率得到N2-n-hexyl-2'-deoxyguanosine
    参考文献:
    名称:
    Structure-activity relationships of N2-substituted guanines as inhibitors of HSV1 and HSV2 thymidine kinases
    摘要:
    A series of N2-phenylguanines was synthesized and tested for inhibition of the thymidine kinases encoded by Herpes simplex viruses type 1 and type 2. Compounds with hydrophobic, electron-attracting groups in the meta position of the phenyl ring such as m-trifluoromethyl (m-CF3PG, IC50 = 0.1 microM) were the most potent inhibitors of both enzymes. Many derivatives were significantly more potent against the type 2 thymidine kinase, and can effectively discriminate between the two enzymes. Among other N2-substituted guanines, alkyl and benzyl derivatives were moderately potent inhibitors, and the type 2 enzyme was again more sensitive than the type 1 enzyme. None of the compounds inhibited the thymidine kinase isolated from the host HeLa cell line, suggesting that members of this class of compounds may be useful nonsubstrate, antiviral compounds for latent herpesvirus infections.
    DOI:
    10.1021/jm00163a033
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