1-(4-methoxyphenyl)-1H-indole-3-carboxylic acid | 1185864-01-0

• 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: 1-(4-methoxyphenyl)-1H-indole-3-carboxylic acid
• 英文别名: 1-(4-methoxyphenyl)indole-3-carboxylic acid
• CAS: 1185864-01-0
• 化学式: C₁₆H₁₃NO₃
• 分子量: 267.284
• InChiKey: YLYSCKHSACFPDP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  51.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-(4-methoxyphenyl)-1H-indole-3-carboxylic acid 在 三乙胺 作用下， 以 甲苯 为溶剂， 反应 5.25h， 生成 1-(2,5-dimethylphenyl)-3-(1-(4-methoxyphenyl)-1H-indol-3-yl)urea
  参考文献：
  名称：

  [EN] COMPOUNDS CONTAINING A HYDROXYPHENYL MOIETY AND THEIR USE
  [FR] COMPOSÉS CONTENANT UNE FRACTION HYDROXYPHÉNYLE ET LEUR UTILISATION

  摘要：

  The inventors have succeeded in developing urea, oxalamide, amide, thiourea, carbamate or ester compounds, in particular urea compounds, bearing two side groups, one of which carries a hydroxyphenyl or phenyl moiety, in particular a hydroxyphenyl moiety. These compounds have the advantage of inhibiting IRE1 RNase activity and sensitizing cancer cells, in particular GB cells, to chemotherapy. The present invention relates to urea, oxalamide, amide, thiourea, carbamate or ester compounds, in particular urea compounds containing a hydroxyphenyl or phenyl moiety, in particular a hydroxyphenyl moiety, including their pharmaceutically acceptable salts and solvates which are useful as sensitizers for chemotherapy of cancer cells, particularly in glioblastoma, and are useful as therapeutic compounds, particularly in the treatment of cancers that may be treated by alkylating agents, such as temozolomide.

  公开号：

  WO2023131677A1
• 作为产物：
  描述：

  4-碘苯甲醚 在 potassium phosphate 、 copper(l) iodide 、 trans-1,2-Diaminocyclohexane 、 水 、 sodium hydroxide 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 甲醇 为溶剂， 生成 1-(4-methoxyphenyl)-1H-indole-3-carboxylic acid
  参考文献：
  名称：

  [EN] COMPOUNDS CONTAINING A HYDROXYPHENYL MOIETY AND THEIR USE
  [FR] COMPOSÉS CONTENANT UNE FRACTION HYDROXYPHÉNYLE ET LEUR UTILISATION

  摘要：

  The inventors have succeeded in developing urea, oxalamide, amide, thiourea, carbamate or ester compounds, in particular urea compounds, bearing two side groups, one of which carries a hydroxyphenyl or phenyl moiety, in particular a hydroxyphenyl moiety. These compounds have the advantage of inhibiting IRE1 RNase activity and sensitizing cancer cells, in particular GB cells, to chemotherapy. The present invention relates to urea, oxalamide, amide, thiourea, carbamate or ester compounds, in particular urea compounds containing a hydroxyphenyl or phenyl moiety, in particular a hydroxyphenyl moiety, including their pharmaceutically acceptable salts and solvates which are useful as sensitizers for chemotherapy of cancer cells, particularly in glioblastoma, and are useful as therapeutic compounds, particularly in the treatment of cancers that may be treated by alkylating agents, such as temozolomide.

  公开号：

  WO2023131677A1

文献信息

• Fused Ring Construction around Pyrrole, Indole, and Related Compounds via Palladium-Catalyzed Oxidative Coupling with Alkynes
  作者：Mana Yamashita、Hakaru Horiguchi、Koji Hirano、Tetsuya Satoh、Masahiro Miura

  DOI：10.1021/jo9016698

  日期：2009.10.2

  palladium-catalyzed oxidative coupling reactions of N-substituted indoles or their carboxylic acid derivatives with alkynes. Unsymmetrically octasubstituted carbazoles can also be obtained by the stepwise couplings of 1-methylpyrrole-2-carboxylic acid with two different alkynes. In addition, the present coupling procedure is applicable to the synthesis of other various heteroarenes possessing di-, tri-, and tetracyclic

  1,2,3,4-四取代咔唑的选择性合成可以通过钯取代的N-取代的吲哚或其羧酸衍生物与炔烃的氧化偶联反应来有效地进行。不对称的八取代咔唑也可以通过1-甲基吡咯-2-羧酸与两种不同炔烃的逐步偶联获得。另外，本偶联方法适用于具有二，三和四环核的其他各种杂芳烃的合成。一些产品在固态下表现出强烈的荧光。
• A condition-tuned unorthodox approach to indole-3-carboxylic acids and anthranilic acids <i>via</i> carbon atom translocation
  作者：Arup Bhowmik、Koushik Naskar、Shantonu Roy、Sudip Karmakar、Writhabrata Sarkar、Imtiaj Mondal、Arindam Sana、Indubhusan Deb

  DOI：10.1039/d3cc04443b

  日期：——

  one-pot cascade method for the synthesis of indole-3-carboxylic acids using isatins and DMSO via a one-carbon translocation involving in situ generation of α,β-unsaturated methylvinylsulfoxide followed by amide bond cleavage and ring closure. The methodology has been extended to afford anthranilic acid derivatives by tuning the reaction conditions in the presence of molecular oxygen. Importantly, easy

  我们描述了一种稳健的一锅级联方法，使用靛红和 DMSO通过一碳易位合成吲哚-3-羧酸，涉及原位生成 α,β-不饱和甲基乙烯基亚砜，然后进行酰胺键断裂和闭环。该方法已扩展到通过在分子氧存在下调整反应条件来提供邻氨基苯甲酸衍生物。重要的是，已证明可以轻松获得商业药物，包括托烷司琼。
• [EN] HEDGEHOG SIGNAL INHIBITOR<br/>[FR] INHIBITEUR DE SIGNAL HEDGEHOG
  申请人：KYOWA HAKKO KIRIN CO LTD

  公开号：WO2011019060A1

  公开（公告）日：2011-02-17

  　下記一般式(I)［式(I)中、R1は、水素原子などを表し、R3は、置換基を有していてもよい低級アルキルなどを表し、Aは、置換基を有していてもよいシクロアルキルなどを表し、Bは、隣接するピロール環の-C=C-と一緒になって、置換基を有していてもよい5または6員環の非芳香族炭素環などを表し、L1は式（i）などを表し、L2は式（iv）（式中、R4は、水素原子などを表す）または式(v)などを表し、Mは式(x)（式中、R2は水素原子などを表し、L2が式（v）などであるとき、Qは存在せず、L2が式（iv）であるとき、Qは存在しないか、または酸素原子を表す）などを表す］で表される縮環複素環誘導体またはその薬学的に許容される塩を有効成分として含有するヘッジホッグシグナル阻害剤などを提供する。