4-fluoro-1-hydroxy-naphthalene-2-carboxylic acid | 1000386-61-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 4-fluoro-1-hydroxy-naphthalene-2-carboxylic acid
• 英文别名: 4-Fluoro-1-hydroxy-2-naphthoic acid；4-fluoro-1-hydroxynaphthalene-2-carboxylic acid
• CAS: 1000386-61-7
• 化学式: C₁₁H₇FO₃
• 分子量: 206.173
• InChiKey: APHBHEVOAHTHFU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  57.5
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  4-氟-1-甲氧基-萘-2-羧酸 在 氢溴酸 、 溶剂黄146 作用下， 反应 1.0h， 生成 4-fluoro-1-hydroxy-naphthalene-2-carboxylic acid
  参考文献：
  名称：

  WO2008/407

  摘要：

  公开号：

文献信息

• Fused bicyclic carboxamide derivates for use as CXCR2 inhibitors in the treatment of inflammation
  申请人：Sanofi-Aventis Deutschland GmbH

  公开号：EP1676834A1

  公开（公告）日：2006-07-05

  The invention relates to compounds of the formula I in which R1, R2, X, A, B, D and Y1 to Y4 have the meanings indicated in the claims, and the pharmaceutically acceptable salts thereof. Because of their properties as inhibitors of chemokine receptors, especially as CXCR2 inhibitors, the compounds of the formula I and the pharmaceutically acceptable salts thereof are suitable for the prevention and treatment of chemokine mediated diseases such as inflammation.

  该发明涉及公式I中的化合物，其中R1、R2、X、A、B、D和Y1至Y4具有索赔中所指示的含义，以及其药用盐。由于它们作为趋化因子受体抑制剂的特性，特别是作为CXCR2抑制剂，公式I中的化合物及其药用盐适用于预防和治疗趋化因子介导的疾病，如炎症。
• INHIBITORS OF CXCR2
  申请人：HACHTEL Stephanie

  公开号：US20090215827A1

  公开（公告）日：2009-08-27

  The invention relates to compounds of the formula I in which R1, R2, X, A, B and Y1 to Y4 have the meanings indicated in the claims, and/or a pharmaceutically acceptable salt and/or a prodrug thereof. Because of their properties as inhibitors of chemokine receptors, especially as CXCR2 inhibitors, the compounds of the formula I and the pharmaceutically acceptable salts and prodrugs thereof are suitable for the prevention and treatment of chemokine mediated diseases.

  该发明涉及公式I的化合物，其中R1，R2，X，A，B和Y1到Y4具有所述权利要求中指示的含义，和/或其药学上可接受的盐和/或前药。由于它们作为趋化因子受体抑制剂的特性，特别是作为CXCR2抑制剂，公式I的化合物和其药学上可接受的盐和前药适用于预防和治疗趋化因子介导的疾病。
• CXCR2 INHIBITORS
  申请人：HACHTEL Stephanie

  公开号：US20090227625A1

  公开（公告）日：2009-09-10

  The invention relates to compounds of the formula I in which R1, R2, X, A, B, Z and Y1 to Y4 have the meanings indicated in the claims, and/or a pharmaceutically acceptable salt and/or a prodrug thereof. Because of their properties as inhibitors of chemokine receptors, especially as CXCR2 inhibitors, the compounds of the formula I and the pharmaceutically acceptable salts and prodrugs thereof are suitable for the prevention and treatment of chemokine mediated diseases.

  本发明涉及公式I的化合物，其中R1、R2、X、A、B、Z和Y1到Y4具有所述权利要求中指示的含义，和/或其药学上可接受的盐和/或前药。由于它们作为趋化因子受体抑制剂的特性，尤其是作为CXCR2抑制剂，公式I的化合物及其药学上可接受的盐和前药适用于预防和治疗趋化因子介导的疾病。
• SUBSTITUTED BENZOYLAMINO-INDAN-2-CARBOXYLIC ACIDS AND RELATED COMPOUNDS
  申请人：CAULFIELD Thomas J.

  公开号：US20100113462A1

  公开（公告）日：2010-05-06

  The present invention relates to novel compounds of the formula I: wherein in any of its stereoisomeric forms or a mixture of stereoisomeric forms in any ratio, or a physiologically acceptable salt thereof, wherein the substituents are as described herein. The inventive compounds have CXCR5 inhibitory activity are particularly useful in treating or preventing various inflammatory diseases, such as rheumatoid arthritis, multiple sclerosis, lupus, Crohn's Disease, associated with the modulation of the human CXCR5 receptor.

  本发明涉及公式I的新化合物：其中在其任何立体异构形式或立体异构形式的混合物中以任何比例，或其生理上可接受的盐，其中取代基如此描述。这些创新化合物具有CXCR5抑制活性，特别适用于治疗或预防各种炎症性疾病，例如类风湿性关节炎，多发性硬化症，红斑狼疮，克罗恩病，与人类CXCR5受体调节相关。
• CXCR2 inhibitors
  申请人：Sanofi-Aventis Deutschland GmbH

  公开号：US08283479B2

  公开（公告）日：2012-10-09

  The invention relates to compounds of the formula I: in which R1, R2, X, A, B, D and Y1 to Y4 have the meanings indicated in the claims, and/or a pharmaceutically acceptable salt and/or a prodrug thereof. Because of their properties as inhibitors of chemokine receptors, especially as CXCR2 inhibitors, the compounds of the formula I and the pharmaceutically acceptable salts and prodrugs thereof are suitable for the prevention and treatment of chemokine mediated diseases.

  本发明涉及I式化合物，其中R1、R2、X、A、B、D和Y1到Y4具有所述权利要求中指定的含义，以及/或其药学上可接受的盐和/或前药。由于它们作为趋化因子受体抑制剂的特性，特别是作为CXCR2抑制剂，I式化合物及其药学上可接受的盐和前药适用于预防和治疗趋化因子介导的疾病。