2-(N-benzoylamino)-5-(2'-deoxy-β-D-ribofuranosyl)pyridine | 166266-29-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-(N-benzoylamino)-5-(2'-deoxy-β-D-ribofuranosyl)pyridine
• 英文别名: 2-(Benzoylamino)-5-(2'-deoxy-β-D-ribofuranosyl)pyridine；N-[5-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyridin-2-yl]benzamide
• CAS: 166266-29-1
• 化学式: C₁₇H₁₈N₂O₄
• 分子量: 314.341
• InChiKey: DCEQPIHNIDJANY-RRFJBIMHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  91.7
• 氢给体数：
  3
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-(N-benzoylamino)-5-(2'-deoxy-β-D-ribofuranosyl)pyridine 在 甲胺 作用下， 反应 25.0h， 以83%的产率得到2-Amino-5-(2'-deoxy-β-D-ribofuranosyl)pyridine
  参考文献：
  名称：

  Hildbrand, Stefan; Leumann, Christian, Angewandte Chemie, 1996, vol. 108, # 17, p. 2100 - 2102

  摘要：

  DOI：
• 作为产物：
  描述：

  2-氨基-5-碘吡啶 在 三(五氟苯基)膦 、 bis(dibenzylideneacetone)-palladium⁽⁰⁾ 吡啶 、 三正丁胺 、 四丁基氟化铵 、 三乙酰氧基硼氢化钠 、 溶剂黄146 作用下， 以 四氢呋喃 、 溶剂黄146 、 乙腈 为溶剂， 反应 26.67h， 生成 2-(N-benzoylamino)-5-(2'-deoxy-β-D-ribofuranosyl)pyridine
  参考文献：
  名称：

  Syntheses of Two Pyridine C-Nucleosides as "Deletion-Modified" Analogs of dT and dC

  摘要：

  DOI：

  10.1021/jo00121a071

文献信息

• Hildbrand, Stefan; Leumann, Christian, Angewandte Chemie, 1996, vol. 108, # 17, p. 2100 - 2102
  作者：Hildbrand, Stefan、Leumann, Christian

  DOI：——

  日期：——
• Syntheses of Two Pyridine C-Nucleosides as "Deletion-Modified" Analogs of dT and dC
  作者：Hsing-Pang Hsieh、Larry W. McLaughlin

  DOI：10.1021/jo00121a071

  日期：1995.8
• 5-Substituted 2-Aminopyridine <i>C</i>-Nucleosides as Protonated Cytidine Equivalents:  Increasing Efficiency and Selectivity in DNA Triple-Helix Formation
  作者：Stefan Hildbrand、Adrian Blaser、Serge P. Parel、Christian J. Leumann

  DOI：10.1021/ja9704904

  日期：1997.6.1

  The easily accessible C-nucleoside 2-amino-5-(2'-deoxy-beta-D-ribofuranosyl)py (P) and its 3-methyl (P-Me) and 2'-O-methyl (P-OMe) derivatives were synthesized and incorporated as protonated cytidine equivalents in homopyrimidine oligodeoxynucleotides. T-m measurements indicate that oligonucleotides containing P or P-Me have a higher affinity to double-stranded DNA over the pH range of 6-8 than, 5-methylcytidine (C-Me) containing oligonucleotides. This increase in stability is most pronounced above pH 7.0. The average increase in T-m/modification for the dissociation of oligonucleotide d((TTTTTPTPTPTPTPT)-P-Me-P-Me-P-Me-P-Me-P-Me) from a 21-mer target duplex at pH 7.5 is 2.3 degrees C relative to oligonucleotide. d((TTTTTCTCTCTCTCT)-C-Me-C-Me-C-Me-C-Me-C-Me). The pH dependence and sequence composition effects are much less pronounced for P-Me (and also P) containing oligonucleotides than for C-Me containing ones. While oligonucleotide d((TTTCCCCTTTTCTTT)-C-Me-C-Me-C-Me-C-Me-C-Me) shows no longer any affinity to the target duplex above pH 6.5, oligonucleotide d((TTTPPPPTTTTPTTT)-P-Me-P-Me-P-Me-P-Me-P-Me) displays preserved binding with a T-m of 32.5 degrees C at pH 7.0 and even binds with a T-m of 23.3 degrees C at pH 8.0. Oligonucleotides containing P-OMe show distinctly less stable triple helices. The average decrease in T-m/modification for oligonucleotide d(TTTPTPOMeTPOMeTPOMeTPOMeTPOMeT) at pH 6.5 is 6.7 degrees C relative to the C-Me containing oligonucleotide. DNase I footprint titration experiments indicate that d((TTTTTPTPTPTPTPT)-P-Me-P-Me-P-Me-P-Me-P-Me) binds not only five times stronger to a 229 base pair DNA fragment than d((TTTTTCTCTCTCTCT)-C-Me-C-Me-C-Me-C-Me-C-Me) but also with higher selectivity; UV-melting experiments show that duplexes of d(TTTTTCTXTCTCTCT) (where X = P, P-Me, or P-OMe) With their antiparallel Watson-Crick complement are dramatically less stable (Delta T-m < -12 degrees C) at pH 8.0 than the corresponding natural duplex. Thus the new bases P and P-Me show Hoogsteen specific pairing behavior.