((S)-4-benzyloxy-3-tert-butoxycarbonylaminobutyl)phosphonic acid diethyl ester | 925706-72-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: ((S)-4-benzyloxy-3-tert-butoxycarbonylaminobutyl)phosphonic acid diethyl ester
• CAS: 925706-72-5
• 化学式: C₂₀H₃₄NO₆P
• 分子量: 415.467
• InChiKey: RWTYMBDSPQHCKD-SFHVURJKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.75
• 重原子数：
  28.0
• 可旋转键数：
  12.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.65
• 拓扑面积：
  83.09
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  ((S)-4-benzyloxy-3-tert-butoxycarbonylaminobutyl)phosphonic acid diethyl ester 在 palladium on activated charcoal ruthenium trichloride 、 sodium periodate 、 氢气 作用下， 以 四氯化碳 、 乙醇 、 水 、 乙腈 为溶剂， 反应 30.0h， 生成 Boc-Abu(PO3Et2)-OH
  参考文献：
  名称：

  Synthesis and biological evaluation of γ-aminophosphonates as potent, subtype-selective sphingosine 1-phosphate receptor agonists and antagonists

  摘要：

  The synthesis of N-arylamide phosphonates and related arylether and arylamine analogues provided potent, subtype-selective agonists and antagonists of the five known sphingosine I-phosphate (SIP) receptors (S1P(1-5)). To this end, the syntheses of phosphoserine mimetics-selectively protected and optically active phosphonoserines-are described. In vitro binding assays showed that the implementation of phosphonates as phosphate mimetics provided compounds with similar receptor binding affinities as compared to their phosphate precursors. meta-substituted arylamide phosphonates were discovered to be antagonists of the S1P(1) and S1P(3) receptors. When administered to mice, an antagonist blocked the lymphopenia evoked by a SIP receptor agonist and caused capillary leakage in both lung and kidney. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2006.10.060
• 作为产物：
  描述：

  ((R)-4-benzyloxy-3-hydroxybutyl)phosphonic acid diethyl ester 在 Lindlar's catalyst 偶氮二甲酸二异丙酯 、 polymer-bound PPh₃ 、 二苯基膦叠氮化物 、 氢气 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 44.0h， 生成 ((S)-4-benzyloxy-3-tert-butoxycarbonylaminobutyl)phosphonic acid diethyl ester
  参考文献：
  名称：

  Synthesis and biological evaluation of γ-aminophosphonates as potent, subtype-selective sphingosine 1-phosphate receptor agonists and antagonists

  摘要：

  The synthesis of N-arylamide phosphonates and related arylether and arylamine analogues provided potent, subtype-selective agonists and antagonists of the five known sphingosine I-phosphate (SIP) receptors (S1P(1-5)). To this end, the syntheses of phosphoserine mimetics-selectively protected and optically active phosphonoserines-are described. In vitro binding assays showed that the implementation of phosphonates as phosphate mimetics provided compounds with similar receptor binding affinities as compared to their phosphate precursors. meta-substituted arylamide phosphonates were discovered to be antagonists of the S1P(1) and S1P(3) receptors. When administered to mice, an antagonist blocked the lymphopenia evoked by a SIP receptor agonist and caused capillary leakage in both lung and kidney. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2006.10.060