| 197974-65-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• CAS: 197974-65-5
• 化学式: C₁₃H₂₃N₆O₂Zn
• 分子量: 360.755
• InChiKey: RKWCXDFSGSLKCW-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
  None
• 环数：
  None
• sp3杂化的碳原子比例：
  None
• 拓扑面积：
  None
• 氢给体数：
  None
• 氢受体数：
  None

反应信息

• 作为反应物：
  描述：

  以 水 为溶剂， 生成
  参考文献：
  名称：

  Facile and Selective Electrostatic Stabilization of Uracil N(1)^- Anion by a Proximate Protonated Amine:  A Chemical Implication for Why Uracil N(1) Is Chosen for Glycosylation Site

  摘要：

  A question of how uracil nitrogen N(1) is selectively activated in enzymes (e.g., for deglycosylation in uracil-DNA glycosylase) has been utterly overlooked, to which we have addressed by a model study with 6-((1,4,7,10-tetraazacyclododecyl)methyl)uracil (HL, cyclen-attached uracil). The uracil N(1)H of the diprotonated cyclen-attached uracil (HL . 2H(+)) is easily deprotonated to be N(1)(-) anion form (L-. 2H(+)) in aqueous solution. The deprotonation constant (pK(a)) of 7.14 for HL . 2H(+) reversible arrow L-. 2H(+) + H+ was determined by potentiometric pH titration at 25 degrees C with I = 0.10 (NaClO4). The unusually low deprotonation constant (cf. pK(a) = 9.9 for 3-methyluracil) is due to the electrostatic stabilization of the N(1)(-) anion by a proximate secondary ammonium cation of the diprotonated cyclen at physiological pH. The X-ray crystal structure of HL . 2H(+) as its dipicrate revealed that the uracil N(1)H is linked by a hydrogen bond network to one of the cyclen secondary ammonium cation through a water. Crystals of HL . 2H(+).(picrate)(2) . H2O (C25H32N12O17) are triclinic, space group P (1) over bar (no. 2) with a = 9.295(4) Angstrom, b = 19.67(1) Angstrom, c = 8.886(6) Angstrom, alpha = 94.36(3)degrees, beta = 102.95(4)degrees, gamma = 87.04(4)degrees, V = 1576(8) Angstrom(3), Z = 2, R = 0.054, and R-W = 0.081. The electrostatic stabilization of uracil N(1)(-) anion is reassessed by a comparative study with a zinc(II) complex with the cyclen-attached uracil, where Zn2+ in the cyclen cavity strongly binds to the uracil N(1)(-) (localized) anion. The deprotonation of N(1)H of HL (1 mM) occurred below pH 5 by the effect of equimolar Zn2+, a stronger acid than two protons. Crystals of the zinc(II) complex (C13H23N6O2Zn . ClO4 . H2O) are triclinic, space group P (1) over bar (no. 2) with a = 9.461(3) Angstrom, b = 13.156(4) Angstrom, c = 8.687(2) Angstrom, alpha = 101.21(2)degrees, beta = 103.55(2)degrees, gamma = 73.21(2)degrees, V = 997(0) Angstrom(3), Z = 2, R = 0.063, and R-W = 0.093. For comparison, we also have investigated the uracil N(1) acidity with an ethylenediamine-attached uracil and an isomeric cyclen-attached (at C(5)) uracil. The present example of electrostatic stabilization of N(1)(-) anion may explain the facile uracil N(1)-alkyl (e.g., glycosyl) bond formation and cleavage in enzymes.

  DOI：

  10.1021/ja972129n
• 作为产物：
  描述：

  以 水 为溶剂， 生成
  参考文献：
  名称：

  Facile and Selective Electrostatic Stabilization of Uracil N(1)^- Anion by a Proximate Protonated Amine:  A Chemical Implication for Why Uracil N(1) Is Chosen for Glycosylation Site

  摘要：

  A question of how uracil nitrogen N(1) is selectively activated in enzymes (e.g., for deglycosylation in uracil-DNA glycosylase) has been utterly overlooked, to which we have addressed by a model study with 6-((1,4,7,10-tetraazacyclododecyl)methyl)uracil (HL, cyclen-attached uracil). The uracil N(1)H of the diprotonated cyclen-attached uracil (HL . 2H(+)) is easily deprotonated to be N(1)(-) anion form (L-. 2H(+)) in aqueous solution. The deprotonation constant (pK(a)) of 7.14 for HL . 2H(+) reversible arrow L-. 2H(+) + H+ was determined by potentiometric pH titration at 25 degrees C with I = 0.10 (NaClO4). The unusually low deprotonation constant (cf. pK(a) = 9.9 for 3-methyluracil) is due to the electrostatic stabilization of the N(1)(-) anion by a proximate secondary ammonium cation of the diprotonated cyclen at physiological pH. The X-ray crystal structure of HL . 2H(+) as its dipicrate revealed that the uracil N(1)H is linked by a hydrogen bond network to one of the cyclen secondary ammonium cation through a water. Crystals of HL . 2H(+).(picrate)(2) . H2O (C25H32N12O17) are triclinic, space group P (1) over bar (no. 2) with a = 9.295(4) Angstrom, b = 19.67(1) Angstrom, c = 8.886(6) Angstrom, alpha = 94.36(3)degrees, beta = 102.95(4)degrees, gamma = 87.04(4)degrees, V = 1576(8) Angstrom(3), Z = 2, R = 0.054, and R-W = 0.081. The electrostatic stabilization of uracil N(1)(-) anion is reassessed by a comparative study with a zinc(II) complex with the cyclen-attached uracil, where Zn2+ in the cyclen cavity strongly binds to the uracil N(1)(-) (localized) anion. The deprotonation of N(1)H of HL (1 mM) occurred below pH 5 by the effect of equimolar Zn2+, a stronger acid than two protons. Crystals of the zinc(II) complex (C13H23N6O2Zn . ClO4 . H2O) are triclinic, space group P (1) over bar (no. 2) with a = 9.461(3) Angstrom, b = 13.156(4) Angstrom, c = 8.687(2) Angstrom, alpha = 101.21(2)degrees, beta = 103.55(2)degrees, gamma = 73.21(2)degrees, V = 997(0) Angstrom(3), Z = 2, R = 0.063, and R-W = 0.093. For comparison, we also have investigated the uracil N(1) acidity with an ethylenediamine-attached uracil and an isomeric cyclen-attached (at C(5)) uracil. The present example of electrostatic stabilization of N(1)(-) anion may explain the facile uracil N(1)-alkyl (e.g., glycosyl) bond formation and cleavage in enzymes.

  DOI：

  10.1021/ja972129n