<2-<2,6-dichloro-3-methoxy-4-(benzyloxy)anilino>phenyl>acetic acid | 127792-41-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: <2-<2,6-dichloro-3-methoxy-4-(benzyloxy)anilino>phenyl>acetic acid
• 英文别名: 2-[(2,6-dichloro-3-methoxy-4-benzyloxyphenyl)amino]phenylacetic acid；2-[2-(2,6-dichloro-3-methoxy-4-phenylmethoxyanilino)phenyl]acetic acid
• CAS: 127792-41-0
• 化学式: C₂₂H₁₉Cl₂NO₄
• 分子量: 432.303
• InChiKey: JPHWBQJFYMSEKT-UHFFFAOYSA-N

物化性质

• 沸点：
  545.6±50.0 °C(Predicted)
• 密度：
  1.370±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.9
• 重原子数：
  29
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  67.8
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  <2-<2,6-dichloro-3-methoxy-4-(benzyloxy)anilino>phenyl>acetic acid 在 钯 2-[(2,6-二氯-3-甲氧基-4-羟基苯基)氨基]苯乙酸 作用下， 以 四氢呋喃 、 邻二氯苯 为溶剂， 反应 0.42h， 以to leave the final product 2-[(2,6-dichloro-3-methoxy-4-hydroxyphenyl)amino]phenylacetic acid的产率得到2-[(2,6-二氯-3-甲氧基-4-羟基苯基)氨基]苯乙酸
  参考文献：
  名称：

  Albumin-binding compounds that prevent nonenzymatic glycation and that may be used for treatment of glycation-related pathologies

  摘要：

  本发明涉及抑制白蛋白非酶促糖基化的组合物，以及使用抑制白蛋白糖基化的化合物治疗糖基化相关病理的方法。

  公开号：

  US06552077B2
• 作为产物：
  描述：

  2-(2-碘苯基)-N,N-二甲基乙酰胺 在 氢氧化钾 、 copper(l) iodide 、 铜 、 potassium carbonate 作用下， 以 乙醇 、 甲苯 为溶剂， 反应 110.0h， 生成 <2-<2,6-dichloro-3-methoxy-4-(benzyloxy)anilino>phenyl>acetic acid
  参考文献：
  名称：

  Synthesis and quantitative structure-activity relationships of diclofenac analogs

  摘要：

  The synthesis of a series of 2-anilinophenylacetic acids, close analogues of diclofenac, is described. These compounds were tested in two models used for evaluating the activity of nonsteroidal antiinflammatory drugs (NSAID's), inhibition of cyclooxygenase enzyme activity in vitro, and adjuvant-induced arthritis (AdA) in rats. Statistically significant correlations were found between the inhibitory activities of the compounds in these two models, indicating that cyclooxygenase inhibition seems to be the underlying mechanism for the antiinflammatory activity of these compounds. Quantitative structure-activity relationship (QSAR) analysis revealed that the crucial parameters for activity in both models were the lipophilicity and the angle of twist between the two phenyl rings. Optimal activities were associated with halogen or alkyl substituents in both ortho positions of the anilino ring. Compounds with OH groups in addition to two ortho substituents or compounds with only one or no ortho substituents were less active.

  DOI：

  10.1021/jm00171a008

文献信息

• ALBUMIN-BINDING COMPOUNDS THAT PREVENT NONENZYMATIC GLYCATION AND THAT MAY BE USED FOR TREATMENT OF GLYCATION-RELATED PATHOLOGIES
  申请人：EXOCELL, INC.

  公开号：EP1242069A2

  公开（公告）日：2002-09-25
• US6355680B1
  申请人：——

  公开号：US6355680B1

  公开（公告）日：2002-03-12
• US6552077B2
  申请人：——

  公开号：US6552077B2

  公开（公告）日：2003-04-22
• [EN] ALBUMIN-BINDING COMPOUNDS THAT PREVENT NONENZYMATIC GLYCATION AND THAT MAY BE USED FOR TREATMENT OF GLYCATION-RELATED PATHOLOGIES<br/>[FR] COMPOSES LIANT L'ALBUMINE QUI EMPECHENT LA GLYCATION NON ENZYMATIQUE ET QUI PEUVENT ETRE UTILISES DANS LE TRAITEMENT DE PATHOLOGIES LIEES A LA GLYCATION
  申请人：EXOCELL INC

  公开号：WO2001003684A2

  公开（公告）日：2001-01-18

  The present invention is directed to compositions, comprising substituted 2(pheryl amino) pheryl acetic acid compounds, that inhibit the nonenzymatic glycation of albumin, as well as methods of using compounds that inhibit albumin glycation for the treatment of glycation-related pathologies including renol vascular dysfunction.
• Synthesis and quantitative structure-activity relationships of diclofenac analogs
  作者：Peter Moser、Alfred Sallmann、Irmgard Wiesenberg

  DOI：10.1021/jm00171a008

  日期：1990.9

  The synthesis of a series of 2-anilinophenylacetic acids, close analogues of diclofenac, is described. These compounds were tested in two models used for evaluating the activity of nonsteroidal antiinflammatory drugs (NSAID's), inhibition of cyclooxygenase enzyme activity in vitro, and adjuvant-induced arthritis (AdA) in rats. Statistically significant correlations were found between the inhibitory activities of the compounds in these two models, indicating that cyclooxygenase inhibition seems to be the underlying mechanism for the antiinflammatory activity of these compounds. Quantitative structure-activity relationship (QSAR) analysis revealed that the crucial parameters for activity in both models were the lipophilicity and the angle of twist between the two phenyl rings. Optimal activities were associated with halogen or alkyl substituents in both ortho positions of the anilino ring. Compounds with OH groups in addition to two ortho substituents or compounds with only one or no ortho substituents were less active.