苄基(1-(二苯氧基磷酰基)己基)氨基甲酸酯 | 143646-45-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 苄基(1-(二苯氧基磷酰基)己基)氨基甲酸酯
• 英文名称: (1-Benzyloxycarbonylamino-hexyl)-phosphonic acid diphenyl ester
• 英文别名: benzyl N-(1-diphenoxyphosphorylhexyl)carbamate
• CAS: 143646-45-1
• 化学式: C₂₆H₃₀NO₅P
• 分子量: 467.502
• InChiKey: KCNURYCZIMNKFF-UHFFFAOYSA-N

物化性质

• 沸点：
  597.2±50.0 °C(Predicted)
• 密度：
  1.183±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.8
• 重原子数：
  33
• 可旋转键数：
  13
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  73.9
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  苄基(1-(二苯氧基磷酰基)己基)氨基甲酸酯 在 盐酸 作用下， 生成 α-aminohexanephosphonic acid
  参考文献：
  名称：

  Cameron, David G.; Hudson, Harry R.; Pianka, Max, Phosphorus, Sulfur and Silicon and the Related Elements, 1993, vol. 83, # 1-4, p. 21 - 38

  摘要：

  DOI：
• 作为产物：
  描述：

  亚磷酸三苯酯 、 氨基甲酸苄酯 、 正己醛 在 tetrafluoroboric acid diethyl ether complex 作用下， 以 乙腈 为溶剂， 生成 苄基(1-(二苯氧基磷酰基)己基)氨基甲酸酯
  参考文献：
  名称：

  具有潜在生物活性的新型1-异硫氰基-烷基膦酸酯二苯酯衍生物的便捷合成

  摘要：

  在这里，我们描述了一种方便的方法，用于合成新的1-异硫氰基-烷基膦酸酯二芳基酯衍生物及其抗增殖活性。合成是基于在碱性条件下使用二硫化碳原位获得的二硫代氨基甲酸酯，以及使用几种不同的试剂对其进行脱硫的方法，其中过氧化氢被证明是最有效的。合成的化合物在体外对几种癌细胞系显示出高抗增殖活性，并且还显示出一些作为丝氨酸蛋白酶抑制剂的活性。

  DOI：

  10.1016/j.tetlet.2012.08.037

文献信息

• New aromatic monoesters of α-aminoaralkylphosphonic acids as inhibitors of aminopeptidase N/CD13
  作者：Renata Grzywa、Anna M. Sokol、Marcin Sieńczyk、Magdalena Radziszewicz、Beata Kościołek、Michael P. Carty、Józef Oleksyszyn

  DOI：10.1016/j.bmc.2010.02.056

  日期：2010.4

  A series of new aromatic monoesters of α-aminoaralkylphosphonic acids were synthesized by selective hydrolysis of corresponding aromatic diesters of α-aminoaralkylphosphonic acids. New potential inhibitors of aminopeptidase N/CD13, an enzyme important in tumour angiogenesis, were developed. Some derivatives of the homophenylalanine and norleucine related monoaryl phosphonates displayed higher inhibition

  通过选择性水解相应的α-氨基芳烷基膦酸芳族二酯，合成了一系列新的α-氨基芳烷基膦酸芳族单酯。开发了新的潜在的氨基肽酶N / CD13抑制剂，这是一种在肿瘤血管生成中很重要的酶。高苯丙氨酸和正亮氨酸相关的单芳基膦酸酯的一些衍生物显示出比相应的α-氨基芳烷基膦酸对氨基肽酶N / CD13更高的抑制能力。单独或与TNF-α一起检测了一种新抑制剂对人PANC-1和HT-1080细胞系生长的影响。
• Remote Binding Energy in Antibody Catalysis:  Studies of a Catalytically Unoptimized Specificity Pocket
  作者：Herschel Wade、Thomas S. Scanlan

  DOI：10.1021/ja983017e

  日期：1999.2.1

  Binding interactions remote from the hydrolytic reaction center have been probed with substrate and phosphonate transition state analogues to understand how these types of interactions are used to promote catalysis in the 17E8 system, We find that the hapten-generated recogniton pocket in 17E8 has properties that are analogous to those of specificity pockets in enzymes, pie have also found that there are specific requirements to form catalytically productive interactions between the side chain and the recognition pocket including conformation, size, and geometry. An additional requirement includes Favorable simultaneous interactions between the side chain and binding packet along with favorable interactions with the oxyanion hole. The 17E8 side chain recognition pocket seems to be less catalytically efficient than analogous pockets in enzymatic systems. The apparent binding energy gained from the methylene-packet interactions in the 17E8 system is significantly smaller than those observed in natural enzymes. Furthermore, 17E8 does not use specific interactions in the recognition pocket to significantly affect catalytic turnover (k(cat)) which is thought to be a trait of an unoptimized catalyst. Analysis of the crystal structure of the 17E8,hapten complex has allowed for the identification of differences between the active sites of 17E8; and several proteases, The identified differences give insight to the sources of the inefficient use of binding energy.