| 162825-91-4

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 嘧啶核苷酸
• CAS: 162825-91-4
• 化学式: C₅₄H₆₀ClN₄O₁₇P
• 分子量: 1103.51
• InChiKey: SVXPMDJNPAUZOV-AWNSJVBLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.54
• 重原子数：
  77.0
• 可旋转键数：
  20.0
• 环数：
  10.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  243.1
• 氢给体数：
  3.0
• 氢受体数：
  18.0

反应信息

• 作为反应物：
  描述：

  、 2-氯苯基二氯膦 在 1H-1,2,4-三唑 、 三乙基碳酸氢铵缓冲液 作用下， 以 吡啶 、 水 为溶剂， 反应 0.25h， 生成
  参考文献：
  名称：

  RNA Modified Uridines VII: Chemical Synthesis and Initial Analysis of tRNA D-Loop Oligomers with Tandem Modified Uridines

  摘要：

  The first chemical synthesis of oligoribonucleotides with adjacent and significantly different modified uridines, the hydrophobic dihydrouridine, D, and the hydrophilic 3-[3-(S)-amino-3-carboxypropyl]-uridine, (acp)U-3, is reported. The trimers Dp-acp(3)UpA, Up-acp(3)UpA, DpUpA and UpUpA, and the dimer Dp-acp(3)U were synthesized and initial structural analysis performed. The synthesis included a combination of protecting groups that is generally applicable to oligonucleotide syntheses in combination with various 2'OH protecting groups. The protecting groups did not cause racemization of the amino acid residue of (acp)3U during deprotection. The assignment of all H-1 NMR resonances of modified nucleoside-containing oligoribonucleotides includes heteronuclear one and two dimensional NMR.

  DOI：

  10.1080/15257779508014659
• 作为产物：
  描述：

  3',5'-O-(1,1,3,3-四异丙基-1,3-二硅氧烷)尿苷 在 对甲苯磺酸 、 triethylamine tris(hydrogen fluoride) 、 1-(mesitylen-2-sulfonyl)-1H-1,2,4-triazole 作用下， 以 四氢呋喃 、 吡啶 为溶剂， 反应 172.0h， 生成
  参考文献：
  名称：

  RNA Modified Uridines VII: Chemical Synthesis and Initial Analysis of tRNA D-Loop Oligomers with Tandem Modified Uridines

  摘要：

  The first chemical synthesis of oligoribonucleotides with adjacent and significantly different modified uridines, the hydrophobic dihydrouridine, D, and the hydrophilic 3-[3-(S)-amino-3-carboxypropyl]-uridine, (acp)U-3, is reported. The trimers Dp-acp(3)UpA, Up-acp(3)UpA, DpUpA and UpUpA, and the dimer Dp-acp(3)U were synthesized and initial structural analysis performed. The synthesis included a combination of protecting groups that is generally applicable to oligonucleotide syntheses in combination with various 2'OH protecting groups. The protecting groups did not cause racemization of the amino acid residue of (acp)3U during deprotection. The assignment of all H-1 NMR resonances of modified nucleoside-containing oligoribonucleotides includes heteronuclear one and two dimensional NMR.

  DOI：

  10.1080/15257779508014659