(2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(1-hydroxyethyl)tetrahydrofuran-3,4-diol | 847659-02-3

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 嘌呤核苷
• 英文名称: (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(1-hydroxyethyl)tetrahydrofuran-3,4-diol
• 英文别名: 9-(6'-deoxy-β-D-allofuranosyl)adenine；1-(6-amino-purin-9-yl)-β-D-1,6-dideoxy-allofuranose；(6'-Deoxy-L-allo-furanosyl)-adenin；(6'-Deoxy-L-talo-furanosyl)adenine；(6'-Deoxy-D-allofuranosyl)adenin；(6'-Deoxy-L-talofuranosyl)adenin；(2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-(1-hydroxyethyl)oxolane-3,4-diol
• CAS: 847659-02-3
• 化学式: C₁₁H₁₅N₅O₄
• 分子量: 281.271
• InChiKey: DJUZHNZMVHIRPJ-ONBHVAQOSA-N

物化性质

• 沸点：
  653.7±65.0 °C(Predicted)
• 密度：
  1.96±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -0.6
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  140
• 氢给体数：
  4
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(1-hydroxyethyl)tetrahydrofuran-3,4-diol 在 barium nitrite 、 溶剂黄146 作用下， 以 水 为溶剂， 反应 168.0h， 以0.25 g的产率得到9-(6-deoxy-β-D-allofuranosyl)hypoxanthine
  参考文献：
  名称：

  Synthesis of hypoxanthine, guanine, and 6-thiopurine nucleosides of 6-deoxy-D-allofuranose

  摘要：

  Hypoxanthine, guanine, and 6-thiopurine nucleosides of 6-deoxy-D-allofuranose have been prepared as potential antitumor agents. Thus, reaction of 6-deoxy-beta-D-allofuranosyl bromide (1) with the trimethylsilyl derivatives of hypoxanthine and guanine afforded mixtures of the 9- and the 7-substituted bases, which were separated and deblocked with ammonia to give 9-(6'-deoxy-beta-D-allofuranosyl)hypoxanthine (6), 7-(6'-deoxy-beta-D-allofuranosyl)hypoxanthine (7), 9-(6'-deoxy-beta-D-allofuranosyl)guanine (8), and 7-(6'-deoxy-beta-D-allofuranosyl)guanine (9). The two nucleosides with the purine joined at the N-9 position, namely, 6 and 8, are easily distinguished from the other two nucleosides (7 and 9), having N-7 junctions, by their NMR spectra. Reaction of 1 with the trimethylsilyl derivative of 6-chloropurine afforded 10, which upon treatment with thiourea and deblocking gave 9-(6'-deoxy-beta-D-allofuranosyl)-6-thiopurine (12). The hypoxanthine and guanine nucleosides showed no inhibition of mouse leukemia L1210 when tested in vivo, but the thiopurine nucleoside 12 showed strong inhibition of growth of L1210 both in vivo and in vitro. Compound 7 strongly inhibited purine nucleoside phosphorylase (KI = 8.8 X 10(-5) M), while compounds 8, 9, 6, and 12 were inactive.

  DOI：

  10.1021/jm00361a023
• 作为产物：
  描述：

  2',3'-isopropylideneadenosine-5'-carboxylic acid 在 N-甲基吗啉 、 ammonium hydroxide 、 sodium tetrahydroborate 、 1-羟基苯并三唑 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 、 三氟乙酸 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 乙醇 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 7.5h， 生成 (2R,3R,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(1-hydroxyethyl)tetrahydrofuran-3,4-diol
  参考文献：
  名称：

  SUBSTITUTED NUCLEOSIDE DERIVATIVES USEFUL AS ANTICANCER AGENTS

  摘要：

  通式（I）的化合物： 制备这些化合物的方法，含有这些化合物的组合物，以及这些化合物的用途。

  公开号：

  US20160244475A1

文献信息

• [EN] SUBSTITUTED NUCLEOSIDE AND NUCLEOTIDE ANALOGS<br/>[FR] NUCLEOSIDE SUBSTITUE ET ANALOGUES NUCLEOTIDIQUES
  申请人：ALIOS BIOPHARMA INC

  公开号：WO2010108140A1

  公开（公告）日：2010-09-23

  Disclosed herein are nucleotide analogs with protected phosphates, methods of synthesizing nucleotide analogs with protected phosphates and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with the nucleotide analogs with protected phosphates.

  本文披露了具有保护磷酸酯基团的核苷酸类似物，以及合成具有保护磷酸酯基团的核苷酸类似物的方法，以及利用具有保护磷酸酯基团的核苷酸类似物治疗病毒感染、癌症和/或寄生虫病等疾病和/或症状的方法。
• SUBSTITUTED NUCLEOTIDE ANALOGS
  申请人：Beigelman Leonid

  公开号：US20120070411A1

  公开（公告）日：2012-03-22

  Disclosed herein are phosphoroamidate nucleotide analogs, methods of synthesizing phosphoroamidate nucleotide analogs and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with the phosphoroamidate nucleotide analogs.

  本文揭示了磷酰胺核苷类似物、合成磷酰胺核苷类似物的方法以及使用磷酰胺核苷类似物治疗病毒感染、癌症和/或寄生虫病等疾病和/或病况的方法。
• SUBSTITUTED NUCLEOSIDE AND NUCLEOTIDE ANALOGS
  申请人：Beigelman Leonid

  公开号：US20100249068A1

  公开（公告）日：2010-09-30

  Disclosed herein are nucleotide analogs with protected phosphates, methods of synthesizing nucleotide analogs with protected phosphates and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with the nucleotide analogs with protected phosphates.

  本文公开了一种具有保护磷酸酯的核苷酸类似物，合成具有保护磷酸酯的核苷酸类似物的方法以及使用具有保护磷酸酯的核苷酸类似物治疗病毒感染、癌症和/或寄生虫病等疾病和/或病况的方法。
• S-adenosyl methionine regulation of metabolic pathways and its use in diagnosis and therapy
  申请人：ORIDIGM CORPORATION

  公开号：EP1221615A2

  公开（公告）日：2002-07-10

  Described is a method to identify a therapeutic composition or protocol which ameliorates a disease or undesired condition in a subject, which method relies upon recognition of the existence of, and the interconnections between, eight SAM pathways shown in Figures 2 - 9, and which acts to restore said SAM pathways toward normality.

  描述了一种确定治疗组合物或方案的方法，这种组合物或方案可改善受试者的疾病或不希望出现的状况，该方法依赖于识别图 2-9 所示的八种 SAM 通路的存在及其之间的相互联系，并使所述 SAM 通路恢复正常。
• Substituted nucleoside and nucleotide analogs
  申请人：Alios Biopharma, Inc.

  公开号：EP2623104A1

  公开（公告）日：2013-08-07

  Disclosed herein are nucleotide analogs with protected phosphates, methods of synthesizing nucleotide analogs with protected phosphates and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with the nucleotide analogs with protected phosphates.

  本文公开了具有受保护磷酸盐的核苷酸类似物、合成具有受保护磷酸盐的核苷酸类似物的方法以及用具有受保护磷酸盐的核苷酸类似物治疗疾病和/或病症（如病毒感染、癌症和/或寄生虫病）的方法。