dimethyl phenoxazine-4,6-dicarboxylate | 120033-22-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并恶嗪类
• 英文名称: dimethyl phenoxazine-4,6-dicarboxylate
• 英文别名: dimethyl 10H-phenoxazine-4,6-dicarboxylate
• CAS: 120033-22-9
• 化学式: C₁₆H₁₃NO₅
• 分子量: 299.283
• InChiKey: ZZLVQLPRLFWBPS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  73.9
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  dimethyl phenoxazine-4,6-dicarboxylate 生成 phenoxazine-4,6-dicarboxylic acid
  参考文献：
  名称：

  4-monosubstituted and 4,6-disubstituted phenoxazines

  摘要：

  4-单取代和4,6-二取代苯氧噻嗪，其制备方法以及含有它们的药物组合物。这些化合物可用作抗炎药。

  公开号：

  US04707473A1
• 作为产物：
  描述：

  吩噁嗪 在 正丁基锂 、 四丁基氟化铵 、 sodium hydride 作用下， 以 四氢呋喃 、 甲醇 、 Petroleum ether 、 苯 为溶剂， 20.0 ℃ 、103.42 kPa 条件下， 反应 12.17h， 生成 dimethyl phenoxazine-4,6-dicarboxylate
  参考文献：
  名称：

  Structure-Based Design of N-Phenyl Phenoxazine Transthyretin Amyloid Fibril Inhibitors

  摘要：

  Starting with the published 2.0 Angstrom X-ray crystal structure of the transthyretin (flufenamic acid)(2) complex, a simple structure-based ligand design strategy was employed to conceive of N-phenyl phenoxazine transthyretin (TTR) amyloid fibril inhibitors. Fifteen N-phenyl phenoxazines were chemically synthesized and evaluated using a quantitative amyloid fibril assay in vitro. The structure of one of the two most active phenoxazines, 4, bound to TTR was solved to a resolution of 1.9 Angstrom to understand the structural basis of its efficacy. N-phenyl phenoxazine 4 binds similar to the orientation anticipated, although not as deeply into the channel as expected. Like flufenamic acid. 4 mediates binding-induced conformational changes that enable intersubunit H-bonding in tetrameric TTR which may be important Tor preventing fibril formation. Analytical ultracentrifugation analysis demonstrates that 4 blocks the first step of TTR amyloid fibril formation, that is, tetramer dissociation to the alternatively folded amyloidogenic monomer. Isothermal titration calorimetry was used to determine the binding constants of 4 to TTR and to dissect the enthalpy and entropy contributions associated with ligand binding. Phenoxazine 4 exhibits binding and inhibitor efficacy against WT TTR that is very similar to that of flufenamic acid, unlike the situation with the inhibition of L55P fibril formation where 4 is superior to Flu as an inhibitor but not as a binder. It is clear that 4 functions in part by stabilizing the normally folded tetramer through formation of the TTR (4)2 complex, which in turn increases the activation energy for tetramer dissociation. The data also suggest that 4 destabilizes the transition state associated with TTR dissociation to the monomeric amyloidogenic intermediate. Future biophysical studies, including kinetic measurements, are needed to understand the exact mechanism(s) of the action of 4.

  DOI：

  10.1021/ja993309v

文献信息

• Regiospecific lithiation of phenoxazine ortho to the oxygen atom. Synthesis of 4-mono- and 4,6-disubstituted phenoxazine derivatives
  作者：Yulia Antonio、Patricia Barrera、Olga Contreras、Fidencio Franco、Edvige Galeazzi、Josefina Garcia、Robert Greenhouse、Angel Guzman、Esperanza Velarde、Joseph M. Muchowski

  DOI：10.1021/jo00270a027

  日期：1989.4
• MUCHOWSKI, JOSEPH M.;GREENHOUSE, ROBERT J.;GUZMAN, ANGEL
  作者：MUCHOWSKI, JOSEPH M.、GREENHOUSE, ROBERT J.、GUZMAN, ANGEL

  DOI：——

  日期：——
• ANTONIO, YULIA;BARRERA, PATRICIA;CONTRERAS, OLGA;FRANCO, FIDENCIO;GALEAZZ+, J. ORG. CHEM., 54,(1989) N, C. 2159-2165
  作者：ANTONIO, YULIA、BARRERA, PATRICIA、CONTRERAS, OLGA、FRANCO, FIDENCIO、GALEAZZ+

  DOI：——

  日期：——
• US4707473A
  申请人：——

  公开号：US4707473A

  公开（公告）日：1987-11-17
• US4803269A
  申请人：——

  公开号：US4803269A

  公开（公告）日：1989-02-07