3-[6-(2-ethoxycarbonyl-vinyl)-2,8-bis-trimethylsilanyl-dibenzofuran-4-yl]-acrylic acid

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并呋喃
• 英文名称: 3-[6-(2-ethoxycarbonyl-vinyl)-2,8-bis-trimethylsilanyl-dibenzofuran-4-yl]-acrylic acid
• 英文别名: (E)-3-[6-[(E)-3-ethoxy-3-oxoprop-1-enyl]-2,8-bis(trimethylsilyl)dibenzofuran-4-yl]prop-2-enoic acid
• 化学式: C₂₆H₃₂O₅Si₂
• 分子量: 480.708
• InChiKey: VZZYKIZLPYJXGJ-WGDLNXRISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.35
• 重原子数：
  33
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  76.7
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-[6-(2-ethoxycarbonyl-vinyl)-2,8-bis-trimethylsilanyl-dibenzofuran-4-yl]-acrylic acid 在 10percent Pd/C 氢气 作用下， 以 甲醇 为溶剂， 20.0 ℃ 、344.75 kPa 条件下， 反应 16.0h， 以100%的产率得到3-[6-(2-ethoxycarbonyl-ethyl)-2,8-bis-trimethylsilanyl-dibenzofuran-4-yl]-propionic acid
  参考文献：
  名称：

  Synthesis of a Negatively Charged Dibenzofuran-Based β-Turn Mimetic and Its Incorporation into the WW Miniprotein-Enhanced Solubility without a Loss of Thermodynamic Stability

  摘要：

  A versatile synthesis has been developed to functionalize the 4-(2-aminoethyl)-6-dibenzofuran propionic acid residue (1a) at the 2 and 8 positions with a variety of different substructures, The unfunctionalized version of this peptidomimetic (1a) is known to facilitate beta-hairpin formation in a variety of small peptides and proteins in aqueous solution when incorporated in place of the i + 1 and i + 2 residues of a U-turn. In this study, we append propionate substituents on 1 a at the 2 and 8 positions to successfully overcome solubility problems encountered with the incorporation of la in place of the i + 1 and i + 2 residues of the beta-turn in loop 1 of the WW domain. The thermodynamic stability of several WW domain analogues incorporating residues 1a and 1b was compared to that of the wild-type sequence revealing comparable DeltaG(H2O) unfolding values at 4 degreesC ranging from 3 to 3.6 kcal/mol. WW domains incorporating residue 1b exhibit improved solubility (exceeding 100 muM) and resistance to aggregation without compromising thermodynamic stability.

  DOI：

  10.1021/ja020675x
• 作为产物：
  描述：

  二苯并呋喃 在 palladium diacetate 、 四甲基乙二胺 、 硫酸 、 碘 、 叔丁基锂 、 仲丁基锂 、 碘酸 、 三乙胺 、 三(邻甲基苯基)磷 作用下， 以 四氢呋喃 、 四氯化碳 、 乙醚 、 溶剂黄146 、 N,N-二甲基甲酰胺 、 正戊烷 为溶剂， 反应 84.17h， 生成 3-[6-(2-ethoxycarbonyl-vinyl)-2,8-bis-trimethylsilanyl-dibenzofuran-4-yl]-acrylic acid
  参考文献：
  名称：

  Synthesis of a Negatively Charged Dibenzofuran-Based β-Turn Mimetic and Its Incorporation into the WW Miniprotein-Enhanced Solubility without a Loss of Thermodynamic Stability

  摘要：

  A versatile synthesis has been developed to functionalize the 4-(2-aminoethyl)-6-dibenzofuran propionic acid residue (1a) at the 2 and 8 positions with a variety of different substructures, The unfunctionalized version of this peptidomimetic (1a) is known to facilitate beta-hairpin formation in a variety of small peptides and proteins in aqueous solution when incorporated in place of the i + 1 and i + 2 residues of a U-turn. In this study, we append propionate substituents on 1 a at the 2 and 8 positions to successfully overcome solubility problems encountered with the incorporation of la in place of the i + 1 and i + 2 residues of the beta-turn in loop 1 of the WW domain. The thermodynamic stability of several WW domain analogues incorporating residues 1a and 1b was compared to that of the wild-type sequence revealing comparable DeltaG(H2O) unfolding values at 4 degreesC ranging from 3 to 3.6 kcal/mol. WW domains incorporating residue 1b exhibit improved solubility (exceeding 100 muM) and resistance to aggregation without compromising thermodynamic stability.

  DOI：

  10.1021/ja020675x

文献信息

• Synthesis of a Negatively Charged Dibenzofuran-Based β-Turn Mimetic and Its Incorporation into the WW Miniprotein-Enhanced Solubility without a Loss of Thermodynamic Stability
  作者：Ramesh Kaul、Songpon Deechongkit、Jeffery W. Kelly

  DOI：10.1021/ja020675x

  日期：2002.10.1

  A versatile synthesis has been developed to functionalize the 4-(2-aminoethyl)-6-dibenzofuran propionic acid residue (1a) at the 2 and 8 positions with a variety of different substructures, The unfunctionalized version of this peptidomimetic (1a) is known to facilitate beta-hairpin formation in a variety of small peptides and proteins in aqueous solution when incorporated in place of the i + 1 and i + 2 residues of a U-turn. In this study, we append propionate substituents on 1 a at the 2 and 8 positions to successfully overcome solubility problems encountered with the incorporation of la in place of the i + 1 and i + 2 residues of the beta-turn in loop 1 of the WW domain. The thermodynamic stability of several WW domain analogues incorporating residues 1a and 1b was compared to that of the wild-type sequence revealing comparable DeltaG(H2O) unfolding values at 4 degreesC ranging from 3 to 3.6 kcal/mol. WW domains incorporating residue 1b exhibit improved solubility (exceeding 100 muM) and resistance to aggregation without compromising thermodynamic stability.