4-bromo-N-(2-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)thiazol-4-yl)-5-methylpicolinamide | 1354412-76-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯并吡啶类
• 英文名称: 4-bromo-N-(2-(4-cyclopropyl-4H-1,2,4-triazol-3-yl)thiazol-4-yl)-5-methylpicolinamide
• 英文别名: 4-bromo-N-[2-(4-cyclopropyl-1,2,4-triazol-3-yl)-1,3-thiazol-4-yl]-5-methylpyridine-2-carboxamide
• CAS: 1354412-76-2
• 化学式: C₁₅H₁₃BrN₆OS
• 分子量: 405.278
• InChiKey: XKTUXRDNCKLZMA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  24
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  114
• 氢给体数：
  1
• 氢受体数：
  6

文献信息

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

  公开号：US20120004267A1

  公开（公告）日：2012-01-05

  The present invention relates to compounds of Formula (I): wherein X 1 , X 2 , X 3 , X 4 , X 5 , R , R 1 , R 2 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, diabetes, diabetic nephropathy, cardio-renal diseases, including kidney disease, fibrotic diseases, respiratory diseases, COPD, idiopathic pulmonary fibrosis, acute lung injury, acute and chronic liver 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).

  本发明涉及以下结构的化合物（I）：其中X1、X2、X3、X4、X5、R、R1、R2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介导的疾病中有用，包括自身免疫性疾病、炎症性疾病、心血管疾病、糖尿病、糖尿病性肾病、心肾疾病、包括肾脏疾病、纤维病性疾病、呼吸系统疾病、慢性阻塞性肺疾病、特发性肺纤维化、急性肺损伤、急性和慢性肝病以及神经退行性疾病。该发明还涉及包含一种或多种化合物的药物组合物（I）以及制备化合物（I）的方法。
• US8440665B2
  申请人：——

  公开号：US8440665B2

  公开（公告）日：2013-05-14
• US8927582B2
  申请人：——

  公开号：US8927582B2

  公开（公告）日：2015-01-06
• USRE48150E1
  申请人：——

  公开号：USRE48150E1

  公开（公告）日：2020-08-11
• [EN] APOPTOSIS SIGNAL-REGULATING KINASE INHIBITORS<br/>[FR] INHIBITEURS DES KINASES RÉGULANT LES SIGNAUX DE L'APOPTOSE
  申请人：GILEAD SCIENCES INC

  公开号：WO2012003387A1

  公开（公告）日：2012-01-05

  The present invention relates to compounds of Formula (I): wherein X1, X2, X3, X4, X5, R, R1, R2 are as defined above. The compounds have apoptosis signal-regulating kinase ("ASKl") inhibitory activity, and are thus useful in the treatment of ASKl -mediated conditions, including autoimmune disorders, inflammatory diseases, cardiovascular diseases, diabetes, diabetic nephropathy, cardio- renal diseases, including kidney disease, fibrotic diseases, respiratory diseases, COPD, idiopathic pulmonary fibrosis, acute lung injury, acute and chronic liver 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).