4-(4'-methoxyphenyl)indoline-2,3-dione | 861389-61-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 4-(4'-methoxyphenyl)indoline-2,3-dione
• 英文别名: 4-(4-methoxyphenyl)-1H-indole-2,3-dione
• CAS: 861389-61-9
• 化学式: C₁₅H₁₁NO₃
• 分子量: 253.257
• InChiKey: NTXZVOWBGZBQDX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  55.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-(4'-methoxyphenyl)indoline-2,3-dione 在 sodium hydroxide 、 双氧水 作用下， 反应 0.5h， 以20%的产率得到6-(4-methoxyphenyl)anthranilic acid
  参考文献：
  名称：

  Direct synthesis of new arylanthranilic acids via a Suzuki cross-coupling reaction from iodoisatins

  摘要：

  Direct synthesis of new arylanthranilic acids via a Suzuki cross-coupling reaction with iodoisatins as key intermediates is described. A 'one pot' procedure is proposed. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2005.04.022
• 作为产物：
  描述：

  3-iodo-isonitrosoacetanilide 在 四(三苯基膦)钯 、 硫酸 、 碳酸氢钠 作用下， 以 乙二醇二甲醚 为溶剂， 生成 4-(4'-methoxyphenyl)indoline-2,3-dione
  参考文献：
  名称：

  Direct synthesis of new arylanthranilic acids via a Suzuki cross-coupling reaction from iodoisatins

  摘要：

  Direct synthesis of new arylanthranilic acids via a Suzuki cross-coupling reaction with iodoisatins as key intermediates is described. A 'one pot' procedure is proposed. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2005.04.022

文献信息

• [EN] CANNABINOID-2-RECEPTOR AGONISTS<br/>[FR] AGONISTES DU RÉCEPTEUR DES CANNABINOÏDES 2
  申请人：ISIS INNOVATION

  公开号：WO2013041859A1

  公开（公告）日：2013-03-28

  The present invention relates to cannabinnoid-2-receptor (CB2R) agonist compounds. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them and to their use as therapeutic agents for the treatment and/or prevention of diseases or conditions in which CB2R stimulation is beneficial (especially inflammatory conditions).

  本发明涉及大麻素-2受体（CB2R）激动剂化合物。本发明还涉及制备这些化合物的方法、包含它们的药物组合物以及它们作为治疗剂用于治疗和/或预防CB2R刺激有益的疾病或状况（尤其是炎症条件）的使用。
• Synthesis and cytotoxic studies of novel 5-phenylisatin derivatives and their anti-migration and anti-angiogenic evaluation
  作者：Qian Zhang、Yuou Teng、Yuan Yuan、Tingting Ruan、Qi Wang、Xing Gao、Yao Zhou、Kailin Han、Peng Yu、Kui Lu

  DOI：10.1016/j.ejmech.2018.07.032

  日期：2018.8

  5-arylisatin derivatives were synthesized in 5-6 steps from readily available starting materials. Their structures were confirmed by 1H NMR and 13C NMR as well as LC/MS. The cytotoxicity of these novel isatins against human leukemia K562 cells were evaluated by MTT assay in vitro. SAR studies indicated that the N-substituted benzyl and C-5 substituted phenyl groups greatly enhance their cytotoxic activity

  从易于获得的起始原料中，以5-6个步骤合成了许多5-arylisatin衍生物。它们的结构通过1 H NMR和13 C NMR以及LC / MS确认。在体外通过MTT分析评估了这些新颖的靛红对人白血病K562细胞的细胞毒性。SAR研究表明，N-取代的苄基和C-5取代的苯基基团大大增强了它们的细胞毒性活性，而保持在母体环上C-3上完整的羰基官能度是必需的。尤其是，N-（对甲氧基苄基）-5-（对甲氧基苯基）Isatin（化合物2m）对K562细胞系表现出最高的抗肿瘤活性（IC50 = 0.03μM）。此外，化合物2m的治疗可显着抑制肝癌HepG2细胞的增殖和迁移，这也可以减少人脐静脉内皮细胞（HUVEC）管的形成。总之，化合物2m在体外通过血管生成反应表现出非常良好的癌细胞增殖抑制作用，并且2m可能是有希望的用于癌症治疗的血管生成抑制剂。
• Cannabinoid-2-Receptor Agonists
  申请人：ISIS INNOVATION LIMITED

  公开号：US20140378451A1

  公开（公告）日：2014-12-25

  The present invention relates to cannabinoid-2-receptor (CB2R) agonist compounds. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them and to their use as therapeutic agents for the treatment and/or prevention of diseases or conditions in which CB2R stimulation is beneficial (especially inflammatory conditions).

  本发明涉及大麻素-2受体（CB2R）激动剂化合物。本发明还涉及这些化合物的制备过程，包括它们在内的药物组合物，以及它们作为治疗剂用于治疗和/或预防CB2R刺激有益的疾病或状况（尤其是炎症条件）的使用。
• Efficient synthesis of bulky 4-substituted-isatins via microwave-promoted Suzuki cross-coupling reaction
  作者：Yu-Chao Liu、Chen-Jin Ye、Qiong Chen、Guang-Fu Yang

  DOI：10.1016/j.tetlet.2012.12.021

  日期：2013.2

  Indoline-2,3-diones (isatins) and their derivatives are important heterocycles found in nature and present in numerous bioactive compounds. Very few examples related to the synthesis of 4-substituted-arylisatins have been reported before. Utilizing microwave irradiation, the synthesis of bulky 4-substituted-arylisatins via a Suzuki cross-coupling has been developed with a wide range of substrates. All the reactions proceeded smoothly and afforded moderate to excellent yields of products, which indicating that electronic effects and steric modifications have little effect on this reaction. (C) 2012 Elsevier Ltd. All rights reserved.
• CANNABINOID-2-RECEPTOR AGONISTS
  申请人：Isis Innovation Limited

  公开号：EP2766022A1

  公开（公告）日：2014-08-20