6-N-benzoyl-P-(2-cyanoethyl)-2'-deoxyadenylyl-(3'->5')-6-N-benzoyl-1',3'-dideoxy-2'-isoadenosine | 787552-78-7

• 分子结构分类: 有机化合物
• 英文名称: 6-N-benzoyl-P-(2-cyanoethyl)-2'-deoxyadenylyl-(3'->5')-6-N-benzoyl-1',3'-dideoxy-2'-isoadenosine
• CAS: 787552-78-7
• 化学式: C₃₇H₃₆N₁₁O₉P
• 分子量: 809.735
• InChiKey: GETAMGVXXBJORX-GMCAOZESSA-N

物化性质

• 密度：
  1.63±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.22
• 重原子数：
  58.0
• 可旋转键数：
  15.0
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.32
• 拓扑面积：
  252.64
• 氢给体数：
  3.0
• 氢受体数：
  18.0

反应信息

• 作为反应物：
  描述：

  6-N-benzoyl-P-(2-cyanoethyl)-2'-deoxyadenylyl-(3'->5')-6-N-benzoyl-1',3'-dideoxy-2'-isoadenosine 在 吡啶 、 四氮唑 、 ammonium hydroxide 、 水 、 碘 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 25.0h， 生成 5'-O-phosphoryl-2'-deoxyadenylyl-(3'->5')-1',3'-dideoxy-2'-isoadenosine
  参考文献：
  名称：

  Inhibition of the strand transfer step of HIV-1 integrase by non-natural dinucleotides

  摘要：

  New, non-natural dinucleotide 5'-monophosphates, with a surrogate isonucleoside component Of L-related stereochemistry at the 'terminal' position, have been synthesized. Structures of 2a-c were confirmed by multinuclear NMR spectra (H-1, C-13, (31)p, COSY), UV hypochromicity and FAB HRMS data. These compounds are totally resistant to cleavage by 3'- and 5'-exonucleases. The dinucleotides showed remarkable selectivity for inhibition of the strand transfer step of HIV-1 integrase. To the best of our knowledge, these compounds represent only the second example of selective strand transfer inhibitors of HIV integrase. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.07.050
• 作为产物：
  描述：

  Phosphoric acid (2R,3S,5R)-5-(6-benzoylamino-purin-9-yl)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-yl ester (2S,4S)-4-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethyl ester 2-cyano-ethyl ester 在 二氯乙酸 作用下， 以 二氯甲烷 为溶剂， 生成 6-N-benzoyl-P-(2-cyanoethyl)-2'-deoxyadenylyl-(3'->5')-6-N-benzoyl-1',3'-dideoxy-2'-isoadenosine
  参考文献：
  名称：

  Inhibition of the strand transfer step of HIV-1 integrase by non-natural dinucleotides

  摘要：

  New, non-natural dinucleotide 5'-monophosphates, with a surrogate isonucleoside component Of L-related stereochemistry at the 'terminal' position, have been synthesized. Structures of 2a-c were confirmed by multinuclear NMR spectra (H-1, C-13, (31)p, COSY), UV hypochromicity and FAB HRMS data. These compounds are totally resistant to cleavage by 3'- and 5'-exonucleases. The dinucleotides showed remarkable selectivity for inhibition of the strand transfer step of HIV-1 integrase. To the best of our knowledge, these compounds represent only the second example of selective strand transfer inhibitors of HIV integrase. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.07.050

文献信息

• Synthetic Approaches to Nuclease-Resistant, Nonnatural Dinucleotides of Anti-Hiv Integrase Interest
  作者：Guochen Chi、Vasu Nair

  DOI：10.1080/15257770500265703

  日期：2005.9.1

  New, nonnatural dinucleotide 5'-monophosphates with a surrogate isonucleoside component of L-related stereochemistry, have been synthesized. Structures of the target compounds were confirmed by multinuclear NMR spectra (H-1, C-13, P-31, COSY), UV hypochromicity, FAB HRMS data and X-ray crystallography. These compounds are totally resistant to cleavage by 3'- and 5'-exonucleases. Dinucleotides of this study with a terminal L-isonucleoside component showed remarkable selectivity for inhibition of the strand transfer step of HIV-1 integrase. To the best of our knowledge, these compounds represent only the second example of this type of selectivity of inhibition of the strand transfer step.