[(2S)-2-amino-3-hydroxypropoxy]phosphonic acid | 1404217-04-4

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机磷酸及其衍生物
• 英文名称: [(2S)-2-amino-3-hydroxypropoxy]phosphonic acid
• 英文别名: [(2S)-2-amino-3-hydroxypropyl] dihydrogen phosphate
• CAS: 1404217-04-4
• 化学式: C₃H₁₀NO₅P
• 分子量: 171.09
• InChiKey: WDWYJNPKBKWDBL-VKHMYHEASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -5.4
• 重原子数：
  10
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  113
• 氢给体数：
  4
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  4-benzyloxy-5H-pyrrolo[3,2-d]pyrimidine-7-carbaldehyde 、 [(2S)-2-amino-3-hydroxypropoxy]phosphonic acid 、 三乙胺 在 2-甲基吡啶-N-甲硼烷 作用下， 以 甲醇 为溶剂， 反应 60.0h， 生成 [(2S)-3-hydroxy-2-[({4-benzyloxy-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]propoxy]phosphonic acid triethylamine salt
  参考文献：
  名称：

  Acyclic phosph(on)ate inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase

  摘要：

  The pathogenic protozoa responsible for malaria lack enzymes for the de novo synthesis of purines and rely on purine salvage from the host. In Plasmodium falciparum (Pf), hypoxanthine-guanine-xanthine phosphoribosyltransferase (HGXPRT) converts hypoxanthine to inosine monophosphate and is essential for purine salvage making the enzyme an anti-malarial drug target. We have synthesized a number of simple acyclic aza-C-nucleosides and shown that some are potent inhibitors of Pf HGXPRT while showing excellent selectivity for the Pf versus the human enzyme. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2013.02.016

文献信息

• Acyclic phosph(on)ate inhibitors of Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase
  作者：Keith Clinch、Douglas R. Crump、Gary B. Evans、Keith Z. Hazleton、Jennifer M. Mason、Vern L. Schramm、Peter C. Tyler

  DOI：10.1016/j.bmc.2013.02.016

  日期：2013.9

  The pathogenic protozoa responsible for malaria lack enzymes for the de novo synthesis of purines and rely on purine salvage from the host. In Plasmodium falciparum (Pf), hypoxanthine-guanine-xanthine phosphoribosyltransferase (HGXPRT) converts hypoxanthine to inosine monophosphate and is essential for purine salvage making the enzyme an anti-malarial drug target. We have synthesized a number of simple acyclic aza-C-nucleosides and shown that some are potent inhibitors of Pf HGXPRT while showing excellent selectivity for the Pf versus the human enzyme. (C) 2013 Elsevier Ltd. All rights reserved.