(S)-9-[3-fluoro-2-(phosphonomethoxy)propyl]-N6-methyladenine | 1305351-61-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并嘧啶类
• 英文名称: (S)-9-[3-fluoro-2-(phosphonomethoxy)propyl]-N6-methyladenine
• CAS: 1305351-61-4
• 化学式: C₁₀H₁₅FN₅O₄P
• 分子量: 319.232
• InChiKey: LTWHKDHBMNOFCQ-SSDOTTSWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.36
• 重原子数：
  21.0
• 可旋转键数：
  7.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  122.39
• 氢给体数：
  3.0
• 氢受体数：
  7.0

反应信息

• 作为产物：
  描述：

  (S)-6-chloro-9-{2-[(diisopropoxyphosphoryl)methoxy]-3-fluoropropyl}purine 在 三甲基溴硅烷 作用下， 以 乙醇 、 乙腈 为溶剂， 生成 (S)-9-[3-fluoro-2-(phosphonomethoxy)propyl]-N6-methyladenine
  参考文献：
  名称：

  Synthesis and antiviral activity of N9-[3-fluoro-2-(phosphonomethoxy)propyl] analogues derived from N6-substituted adenines and 2,6-diaminopurines

  摘要：

  An efficient method for the synthesis of N-9-[3-fluoro-2-(phosphonomethoxy) propyl] (FPMP) derivatives of purine bases has been developed. Both (R)- and (S)-enantiomers of the N-6-substituted FPMP derivatives of adenine and 2,6-diaminopurine were prepared and their anti-human immunodeficiency virus (HIV) and anti-Moloney murine sarcoma virus (MSV) activity was evaluated. Whereas none of the 6-substituted FPMPA derivatives showed any antiviral activity, several FPMPDAP derivatives had a moderate antiretroviral activity. Moreover, the data obtained from the study of the substrate activity of the active derivatives towards N-6-methyl-AMP aminohydrolase support the notion that the studied N-6-substituted FPMPDAP derivatives act as prodrugs of the antiretroviral FPMPG analogues. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.02.050