[2,2'-Bipyridine]-5-carboxamide

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: [2,2'-Bipyridine]-5-carboxamide
• 英文别名: 6-pyridin-2-ylpyridine-3-carboxamide
• 化学式: C₁₁H₉N₃O
• 分子量: 199.21
• InChiKey: IJZLDWAQCDOZMH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  68.9
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• APOPTOSIS SIGNAL-REGULATING KINASE INHIBITORS
  申请人：Corkey Britton

  公开号：US20110009410A1

  公开（公告）日：2011-01-13

  The present invention relates to compounds of Formula (I): where in X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , R 1 , R 2 , R 3 are as defined above. The compounds have apoptosis signal-regulating kinase (“ASK1”) inhibitory activity, and are thus useful in the treatment of ASK1-mediated conditions, including autoimmune disorders, inflammatory diseases, cardiovascular diseases and neurodegenerative diseases. The invention also relates to pharmaceutical compositions comprising one or more of the compounds of Formula (I), and to methods of preparing the compounds of Formula (I).

  本发明涉及式(I)的化合物： 其中X 1 、X 2 、X 3 、X 4 、X 5 、X 6 、X 7 、X 8 、R 1 、R 2 、R 3 如上所定义。这些化合物具有凋亡信号调节激酶（“ASK1”）抑制活性，因此在治疗ASK1介导的疾病，包括自身免疫性疾病、炎症性疾病、心血管疾病和神经退行性疾病方面具有用途。该发明还涉及包含一种或多种式(I)化合物的药物组合物，以及制备式(I)化合物的方法。
• [EN] ARYLALKYLAMINO-SUBSTITUTED QUINAZOLINE ANALOGUES<br/>[FR] ANALOGUES QUINAZOLINE A SUBSTITUTION D'ARYLALKYLAMINO
  申请人：NEUROGEN CORP

  公开号：WO2005087227A1

  公开（公告）日：2005-09-22

  Arylalkylamino-substituted quinazoline analogues are provided, of the Formula wherein variables are as described herein. Such compounds are ligands that may be used to modulate specific receptor activity in vivo or in vitro, and are particularly useful in the treatment of conditions associated with pathological receptor activation in humans, domesticated companion animals and livestock animals. Pharmaceutical compositions and methods for using such compounds to treat such disorders are provided, as are methods for using such ligands for receptor localization studies.

  提供了芳基烷基氨基取代的喹唑啉类似物，其化学式如下，其中变量如本文所述。这些化合物是配体，可用于体内或体外调节特定受体活性，并在治疗人类、驯养伴侣动物和家畜动物中与病理性受体激活相关的疾病方面特别有用。提供了用于治疗这些疾病的药物组合物和方法，以及用于受体定位研究的这类配体的方法。
• Activator of TREK (TWIK RElated K+ channels) channels
  申请人：ONO PHARMACEUTICAL CO., LTD.

  公开号：US11046683B2

  公开（公告）日：2021-06-29

  Disclosed is a compound of formula (I): wherein all symbols are defined in the description. Also disclosed are pharmaceutical compositions comprising the compounds, methods of making the compounds, kits comprising the compounds, and methods of using the compounds, compositions and kits for treatment of disorders associated with TREK-1, TREK-2 or both TREK-1 and TREK-2 dysfunction in a mammal.

  本发明公开了一种式 (I) 的化合物： 其中所有符号在描述中定义。还公开了包含所述化合物的药物组合物、制造所述化合物的方法、包含所述化合物的试剂盒，以及使用所述化合物、组合物和试剂盒治疗哺乳动物中与 TREK-1、TREK-2 或 TREK-1 和 TREK-2 功能障碍相关的疾病的方法。
• SUBSTITUTED QUINAZOLIN-4-YLAMINE ANALOGUES AS MODULATORS OF CAPSAICIN RECEPTORS
  申请人：NEUROGEN CORPORATION

  公开号：EP1471910A2

  公开（公告）日：2004-11-03
• CARBOXYLIC ACID, PHOSPHATE OR PHOSPHONATE SUBSTITUTED QUINAZOLIN-4-YLAMINE ANALOGUES AS CAPSAICIN RECEPTOR MODULATORS
  申请人：NEUROGEN CORPORATION

  公开号：EP1569926A1

  公开（公告）日：2005-09-07