5-methyl-2'-deoxycytydinyl(5'->3')-1'-deoxy-2'-isoadenosine-5'-phosphate

• 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
• 英文名称: 5-methyl-2'-deoxycytydinyl(5'->3')-1'-deoxy-2'-isoadenosine-5'-phosphate
• 英文别名: [(2R,3S,5R)-5-(4-amino-5-methyl-2-oxo-pyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl [(2R,3S,4R)-4-(6-aminopurin-9-yl)-2-(phosphonooxymethyl)tetrahydrofuran-3-yl] hydrogen phosphate；[(2R,3S,5R)-5-(4-amino-5-methyl-2-oxopyrimidin-1-yl)-3-hydroxyoxolan-2-yl]methyl [(2R,3S,4R)-4-(6-aminopurin-9-yl)-2-(phosphonooxymethyl)oxolan-3-yl] hydrogen phosphate
• 化学式: C₂₀H₂₈N₈O₁₂P₂
• 分子量: 634.436
• InChiKey: WPXALMHLULZQDA-RZTQCUEVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -5
• 重原子数：
  42
• 可旋转键数：
  10
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  290
• 氢给体数：
  6
• 氢受体数：
  16

反应信息

• 作为产物：
  描述：

  3'-O-acetylthymidine 在 吡啶 、 二氯乙酸 、 ammonium hydroxide 、 2,4,6-triisopropylbenzenesulfonyl tetrazolide 作用下， 以 二氯甲烷 为溶剂， 反应 9.55h， 生成 5-methyl-2'-deoxycytydinyl(5'->3')-1'-deoxy-2'-isoadenosine-5'-phosphate
  参考文献：
  名称：

  Recognition and Inhibition of HIV Integrase by Novel Dinucleotides

  摘要：

  HIV integrase is involved in the integration of viral DNA into chromosomal DNA, a biological process that occurs by a sequence involving HIV DNA splicing and subsequent integration steps. in the quest for small nucleotide systems with nuclease stability of the internucleotide phosphate bond and critical structural features for recognition and inhibition of HIV-1 integrase, we have discovered novel, nuclease-resistant dinucleotides with defined base sequences that are inhibitors of this key viral enzyme. Synthetic methodologies utilized for the syntheses of the novel dinucleotides include an excellent new phosphorylating agent.

  DOI：

  10.1021/ja992528d

文献信息

• Recognition and Inhibition of HIV Integrase by Novel Dinucleotides
  作者：Michael Taktakishvili、Nouri Neamati、Yves Pommier、Suresh Pal、Vasu Nair

  DOI：10.1021/ja992528d

  日期：2000.6.1

  HIV integrase is involved in the integration of viral DNA into chromosomal DNA, a biological process that occurs by a sequence involving HIV DNA splicing and subsequent integration steps. in the quest for small nucleotide systems with nuclease stability of the internucleotide phosphate bond and critical structural features for recognition and inhibition of HIV-1 integrase, we have discovered novel, nuclease-resistant dinucleotides with defined base sequences that are inhibitors of this key viral enzyme. Synthetic methodologies utilized for the syntheses of the novel dinucleotides include an excellent new phosphorylating agent.