2,6-dichloro-9-(2,3-dideoxy-β-D-glyceropentofuranosyl)-9H-purine | 500342-57-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2,6-dichloro-9-(2,3-dideoxy-β-D-glyceropentofuranosyl)-9H-purine
• CAS: 500342-57-4
• 化学式: C₁₈H₁₆Cl₂N₄O₃
• 分子量: 407.256
• InChiKey: CJLHKFMKMXPJJM-QWHCGFSZSA-N

物化性质

• 沸点：
  527.8±60.0 °C(Predicted)
• 密度：
  1.55±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.98
• 重原子数：
  27.0
• 可旋转键数：
  4.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  79.13
• 氢给体数：
  0.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  2,6-dichloro-9-(2,3-dideoxy-β-D-glyceropentofuranosyl)-9H-purine 在 palladium on activated charcoal sodium hydroxide 、 氢气 作用下， 以 乙醇 为溶剂， 20.0~60.0 ℃ 、344.74 kPa 条件下， 反应 34.0h， 生成 6-cycloheptylamino-9-(2,3-dideoxy-β-D-glyceropentofuranosyl)-9H-purine
  参考文献：
  名称：

  Adenine and Deazaadenine Nucleoside and Deoxynucleoside Analogues: Inhibition of Viral Replication of Sheep MVV (In Vitro Model for HIV) and Bovine BHV-1

  摘要：

  A series of N-6-cycloalkyl-2',3'-dideoxyadenosine derivatives has been prepared by coupling of 2,6-dichloropurine to protected 2,3-dideoxyribose. followed by reaction with appropriate cycloalkylamines. Synthesized compounds, along with other purine nucleoside analogues previously synthesized in our laboratory. have been tested for their antiviral activity against Bovine herpesvirus 1 (BHV-1) and sheep Maedi/Visna Virus (MVV). the latter being an in vitro and in vivo model of Human Immunodeficiency Virus (HIV). All compounds showed good antireplicative activity against MVV. with the N-6-cycloheptyl-2'.3-dideoxy-adenosine (5b) being the most active [effective concentration (EC50) causing 50% reduction of cytopatic effects (CP) = 27 nM]. All compounds showed also a from tow to very low cell toxicity. resulting in a cytotoxic dose 50 (CD50)/EC50 ratio in some cases higher than 1000. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(02)00131-1
• 作为产物：
  描述：

  2,6-二氯嘌呤 在 硫酸氢铵 、 TMSTf 作用下， 以 二氯甲烷 为溶剂， 反应 5.0h， 生成 2,6-dichloro-9-(2,3-dideoxy-β-D-glyceropentofuranosyl)-9H-purine
  参考文献：
  名称：

  Adenine and Deazaadenine Nucleoside and Deoxynucleoside Analogues: Inhibition of Viral Replication of Sheep MVV (In Vitro Model for HIV) and Bovine BHV-1

  摘要：

  A series of N-6-cycloalkyl-2',3'-dideoxyadenosine derivatives has been prepared by coupling of 2,6-dichloropurine to protected 2,3-dideoxyribose. followed by reaction with appropriate cycloalkylamines. Synthesized compounds, along with other purine nucleoside analogues previously synthesized in our laboratory. have been tested for their antiviral activity against Bovine herpesvirus 1 (BHV-1) and sheep Maedi/Visna Virus (MVV). the latter being an in vitro and in vivo model of Human Immunodeficiency Virus (HIV). All compounds showed good antireplicative activity against MVV. with the N-6-cycloheptyl-2'.3-dideoxy-adenosine (5b) being the most active [effective concentration (EC50) causing 50% reduction of cytopatic effects (CP) = 27 nM]. All compounds showed also a from tow to very low cell toxicity. resulting in a cytotoxic dose 50 (CD50)/EC50 ratio in some cases higher than 1000. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(02)00131-1

文献信息

• Deaza- and Deoxyadenosine Derivatives: Synthesis and Inhibition of Animal Viruses as Human Infection Models
  作者：Sauro Vittori、Daniela Salvatori、Rosaria Volpini、Silvia Vincenzetti、Alberto Vita、Sara Taffi、Stefano Costanzi、Catia Lambertucci、Gloria Cristalli

  DOI：10.1081/ncn-120022676

  日期：2003.10

  N-6-Cycloalkyl-2',3'-dideoxyadenosine derivatives and (2-chloro)-N-6-cycloheptyl-3-deazaadenosine have been synthesized and tested, along with other (deaza)purine (deoxy)nucleosides from our chemical library, as inhibitors of virus replication against Bovine Herpes Virus 1 (BHV-1) and sheep Maedi/Visna Virus (MVV). Most compounds demonstrated good antireplicative activity against MVV, showing also low cell toxicity.