(2R,3S,4S,5R)-2-Hydroxymethyl-5-(5-methylsulfanyl-1-thia-2,4,6-triaza-pentalen-4-yl)-tetrahydro-furan-3,4-diol

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2R,3S,4S,5R)-2-Hydroxymethyl-5-(5-methylsulfanyl-1-thia-2,4,6-triaza-pentalen-4-yl)-tetrahydro-furan-3,4-diol
• 英文别名: 2-Hydroxymethyl-5-(5-methylsulfanyl-1-thia-2,4,6-triaza-pentalen-4-yl)-tetrahydro-furan-3,4-diol；(2R,3S,4S,5R)-2-(hydroxymethyl)-5-(5-methylsulfanylimidazo[4,5-d][1,2]thiazol-4-yl)oxolane-3,4-diol
• 化学式: C₁₀H₁₃N₃O₄S₂
• 分子量: 303.363
• InChiKey: DLBRRSUNJFUPDX-JAGXHNFQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.1
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  154
• 氢给体数：
  3
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  4-((3S,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-5-methylsulfanyl-4H-1-thia-2,4,6-triaza-pentalene 在 三氯化硼 作用下， 以 二氯甲烷 为溶剂， 反应 2.0h， 以39%的产率得到(2R,3S,4S,5R)-2-Hydroxymethyl-5-(5-methylsulfanyl-1-thia-2,4,6-triaza-pentalen-4-yl)-tetrahydro-furan-3,4-diol
  参考文献：
  名称：

  Synthesis, Antiproliferative and Antiviral Activity of Imidazo[4,5-d]isothiazole Nucleosides as 5:5 Fused Analogs of Nebularine and 6-Methylpurine Ribonucleoside

  摘要：

  A series of imidazo[4,5-d]isothiazole nucleosides related to the antibiotic nebularine and the highly cytotoxic 6-methyl-9-beta-D-ribofuranosylpurine have been synthesized from the corresponding heterocycles. The sodium salt glycosylation of the imidazo[4,5-d]isothiazoles proceeded smoothly, giving mixtures of N-4 and N-6 regioisomers in generally good yields. The protected derivatives were deblocked using standard conditions to afford the desired imidazo[4,5-d]isothiazole nucleosides, usually as crystalline solids. None of the new nucleosides or heterocycles displayed selective activity against human cytomegalovirus (HCMV) or herpes simplex virus type 1 (HSV-1). The N-6 glycosylated imidazo[4,5-d]isothiazoles were completely inactive up to the highest concentration tested. The N-6 glycosylated imidazo[4,5-d]isothiazoles also were inactive in antiproliferative and cytotoxicity assays, except for 3-methyl-6-beta-D-ribofuranosylimidazo[4,5-d]isothiazole (15a) and 5-(benzylthio)-6-(2-deoxy-beta-D-ribofuranosyl)imidazo[4,5-d]isothiazole (5e), which showed moderate inhibition of L1210 cell growth. However, the heterocycles and several of the N-4 glycosylated derivatives were toxic to HFF, KB and L1210 cells; compounds with 5-benzylthio substituents were the most cytotoxic agents in this series.

  DOI：

  10.1021/jm960605z

文献信息

• Synthesis, Antiproliferative and Antiviral Activity of Imidazo[4,5-<i>d</i>]isothiazole Nucleosides as 5:5 Fused Analogs of Nebularine and 6-Methylpurine Ribonucleoside
  作者：Eric E. Swayze、John C. Drach、Linda L. Wotring、Leroy B. Townsend

  DOI：10.1021/jm960605z

  日期：1997.2.1

  A series of imidazo[4,5-d]isothiazole nucleosides related to the antibiotic nebularine and the highly cytotoxic 6-methyl-9-beta-D-ribofuranosylpurine have been synthesized from the corresponding heterocycles. The sodium salt glycosylation of the imidazo[4,5-d]isothiazoles proceeded smoothly, giving mixtures of N-4 and N-6 regioisomers in generally good yields. The protected derivatives were deblocked using standard conditions to afford the desired imidazo[4,5-d]isothiazole nucleosides, usually as crystalline solids. None of the new nucleosides or heterocycles displayed selective activity against human cytomegalovirus (HCMV) or herpes simplex virus type 1 (HSV-1). The N-6 glycosylated imidazo[4,5-d]isothiazoles were completely inactive up to the highest concentration tested. The N-6 glycosylated imidazo[4,5-d]isothiazoles also were inactive in antiproliferative and cytotoxicity assays, except for 3-methyl-6-beta-D-ribofuranosylimidazo[4,5-d]isothiazole (15a) and 5-(benzylthio)-6-(2-deoxy-beta-D-ribofuranosyl)imidazo[4,5-d]isothiazole (5e), which showed moderate inhibition of L1210 cell growth. However, the heterocycles and several of the N-4 glycosylated derivatives were toxic to HFF, KB and L1210 cells; compounds with 5-benzylthio substituents were the most cytotoxic agents in this series.