S²-(β-D-ribofuranosyl)-2-mercapto-5,6-dichlorobenzimidazole

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: S²-(β-D-ribofuranosyl)-2-mercapto-5,6-dichlorobenzimidazole
• 英文别名: (2S,3R,4S,5R)-2-[(5,6-dichloro-1H-benzimidazol-2-yl)sulfanyl]-5-(hydroxymethyl)oxolane-3,4-diol
• 化学式: C₁₂H₁₂Cl₂N₂O₄S
• 分子量: 351.21
• InChiKey: OAIQKPGSRCSLSD-DBIOUOCHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  21
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  124
• 氢给体数：
  4
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  邻二氯苯 在 镍 氢氧化钾 、 三氟甲磺酸三甲基硅酯 、 硫酸 、 三氧化硫 、 氨 、 氢气 、 硝酸 作用下， 以 甲醇 、 乙醇 、 1,2-二氯乙烷 为溶剂， 反应 46.5h， 生成 S²-(β-D-ribofuranosyl)-2-mercapto-5,6-dichlorobenzimidazole
  参考文献：
  名称：

  Synthesis and Antiviral Evaluation of 2-Mercapto-5,6-dichlorobenzimidazole-β-D-ribofuranonucleoside Derivatives

  摘要：

  2-Mercapto-5,6-dichlorobenzimidazole beta-D-ribofuranonucleoside derivatives 8-10 have been synthesized and their antiviral properties examined. According to the glycosylation procedure used, the beta-D-N-1 isomer (and the N,N-bis-riboside) or the beta D-S-2-isomer have been obtained. All the prepared compounds were tested for their activity against a variety of RNA and DNA viruses, but they did not show significant antiviral activity.

  DOI：

  10.1080/15257779408013253

文献信息

• Synthesis and Antiviral Evaluation of 2-Mercapto-5,6-dichlorobenzimidazole-β-D-ribofuranonucleoside Derivatives
  作者：C. Mathé、C. Périgaud、G. Gosselin、J.-L. Imbach

  DOI：10.1080/15257779408013253

  日期：1994.3

  2-Mercapto-5,6-dichlorobenzimidazole beta-D-ribofuranonucleoside derivatives 8-10 have been synthesized and their antiviral properties examined. According to the glycosylation procedure used, the beta-D-N-1 isomer (and the N,N-bis-riboside) or the beta D-S-2-isomer have been obtained. All the prepared compounds were tested for their activity against a variety of RNA and DNA viruses, but they did not show significant antiviral activity.