(2R,4S,5S)-2-azidoethyl-5-[(1R,2R,3R,4R)-2,3-dihydroxy-4-(uracil-1-yl)]tetrahydrofuryl-3-palmitoyl-(1,3)-oxazolidine-4-carboxylic acid | 1223563-83-4

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (2R,4S,5S)-2-azidoethyl-5-[(1R,2R,3R,4R)-2,3-dihydroxy-4-(uracil-1-yl)]tetrahydrofuryl-3-palmitoyl-(1,3)-oxazolidine-4-carboxylic acid
• 英文别名: (2R,4S,5S)-2-(2-azidoethyl)-5-[(2S,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]-3-hexadecanoyl-1,3-oxazolidine-4-carboxylic acid
• CAS: 1223563-83-4
• 化学式: C₃₀H₄₈N₆O₉
• 分子量: 636.746
• InChiKey: VUWGWGOUAMHHBZ-TYDZDBEGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.4
• 重原子数：
  45
• 可旋转键数：
  20
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  180
• 氢给体数：
  4
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  (2R,4S,5S)-2-azidoethyl-5-[(1R,2R,3R,4R)-2,3-dihydroxy-4-(uracil-1-yl)]tetrahydrofuryl-3-palmitoyl-(1,3)-oxazolidine-4-carboxylic acid 在 Pearlman's catalist 、 氢气 作用下， 以 甲醇 为溶剂， 反应 3.0h， 以68%的产率得到(2R,4S,5S)-2-aminoethyl-5-[(1R,2R,3R,4R)-2,3-dihydroxy-4-(uracil-1-yl)]tetrahydrofuryl-3-palmitoyl-(1,3)-oxazolidine-4-carboxylic acid
  参考文献：
  名称：

  Function-Oriented Synthesis of Simplified Caprazamycins: Discovery of Oxazolidine-Containing Uridine Derivatives as Antibacterial Agents against Drug-Resistant Bacteria

  摘要：

  The rational simplification of the caprazamycin (CPZ) class of nucleoside natural products was carried out to address their molecular complexity. First, analogues 6-8, where the diazepanone ring of the CPZ was removed and a lipophilic side chain was attached to either the C-7' or N(6') atom, were used to investigate the conformation activity relationship. On the basis of this relationship, we designed the oxazolidine-containing uridine derivatives 18-21 by restricting the conformation of 6-8. As a result, the 'Bu ester derivatives 20 were found to be the most active against a range of bacterial strains containing VRE with a potency similar to that of the parent CPZs. This study provides a novel strategy for the development of a new type of antibacterial agent effective against drug-resistant bacteria.

  DOI：

  10.1021/jm100243n
• 作为产物：
  描述：

  (2R,4S,5S)-2-azidoethyl-5-[(1R,2R,3R,4R)-2,3-di-tert-butyldimethylsilyloxy-4-(uracil-1-yl)]tetrahydrofuryl-3-palmitoyl-(1,3)-oxazolidine-4-carboxylic acid 在 triethylamine tris(hydrogen fluoride) 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 80.0h， 以92%的产率得到(2R,4S,5S)-2-azidoethyl-5-[(1R,2R,3R,4R)-2,3-dihydroxy-4-(uracil-1-yl)]tetrahydrofuryl-3-palmitoyl-(1,3)-oxazolidine-4-carboxylic acid
  参考文献：
  名称：

  Function-Oriented Synthesis of Simplified Caprazamycins: Discovery of Oxazolidine-Containing Uridine Derivatives as Antibacterial Agents against Drug-Resistant Bacteria

  摘要：

  The rational simplification of the caprazamycin (CPZ) class of nucleoside natural products was carried out to address their molecular complexity. First, analogues 6-8, where the diazepanone ring of the CPZ was removed and a lipophilic side chain was attached to either the C-7' or N(6') atom, were used to investigate the conformation activity relationship. On the basis of this relationship, we designed the oxazolidine-containing uridine derivatives 18-21 by restricting the conformation of 6-8. As a result, the 'Bu ester derivatives 20 were found to be the most active against a range of bacterial strains containing VRE with a potency similar to that of the parent CPZs. This study provides a novel strategy for the development of a new type of antibacterial agent effective against drug-resistant bacteria.

  DOI：

  10.1021/jm100243n