4-(3-phenylphenyl)-5H-imidazo[4,5-c]pyridazine

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-(3-phenylphenyl)-5H-imidazo[4,5-c]pyridazine
• 化学式: C₁₇H₁₂N₄
• 分子量: 272.3
• InChiKey: DYPBSSSLPCNNAT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  21
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  54.5
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• Chemical Compounds
  申请人：Pfizer Limited

  公开号：US20140171435A1

  公开（公告）日：2014-06-19

  The present invention relates to imidazopyridazine derivatives. More particularly, it relates to 4-(biphenyl-3-yl)-7H-imidazo[4,5-c]pyridazine derivatives of formula (I): and pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 3 , R 4 and R 5 are as defined in the description. The imidazopyridazine derivatives of the present invention modulate the activity of the GABA A receptor. They are useful in the treatment of a number of conditions, including pain.

  本发明涉及咪唑吡啶并嗪衍生物。更具体地，涉及式(I)的4-(联苯基-3-基)-7H-咪唑并嗪衍生物及其药学上可接受的盐，其中R1、R2、R3、R4和R5如描述中所定义。本发明的咪唑吡啶并嗪衍生物调节GABA A 受体的活性。它们在治疗多种疾病，包括疼痛方面具有用处。
• [EN] IMIDAZOPYRIDAZINE DERIVATIVES AS MODULATORS OF THE GABAA RECEPTOR ACTIVITY.<br/>[FR] DÉRIVÉS D'IMIDAZOPYRIDAZINE UTILISÉS COMME MODULATEURS DE L'ACTIVITÉ DES RÉCEPTEURS GABAA.
  申请人：PFIZER LTD

  公开号：WO2015189744A1

  公开（公告）日：2015-12-17

  The present invention relates to imidazopyridazine derivatives. More particularly, it relates to 4-(biphenyl-3-yl)-7H-imidazo[4,5-c]pyridazine derivatives of formula (I) and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R and R6 are as defined in the description. The imidazopyridazine derivatives of the present invention modulate the activity of the GABAA receptor. They are useful in the treatment of a number of conditions, including pain.

  本发明涉及咪唑吡啶并嗪衍生物。更具体地，涉及式(I)的4-(联苯基-3-基)-7H-咪唑并嗪衍生物及其药学上可接受的盐，其中R1、R2、R3、R4、R和R6如描述中所定义。本发明的咪唑吡啶并嗪衍生物调节GABAA受体的活性。它们在治疗多种疾病，包括疼痛方面具有用处。
• [EN] 4-(BIPHEN-3-YL)-1H-PYRAZOLO[3,4-C]PYRIDAZINE DERIVATIVES OF FORMULA (I) AS GABA RECEPTOR MODULATORS FOR USE IN THE TREATMENT OF EPILEPSY AND PAIN<br/>[FR] DÉRIVÉS 4-(BIPHÉNYL-3-YL)-1H-PYRAZOLO[3,4-C]PYRIDAZINE DE FORMULE (I) UTILISÉS COMME MODULATEURS DE RÉCEPTEUR GABA POUR LE TRAITEMENT DE L'ÉPILEPSIE ET DE LA DOULEUR
  申请人：PFIZER LTD

  公开号：WO2017098367A1

  公开（公告）日：2017-06-15

  The present invention relates to pyrazolopyridazine derivatives. More particularly, it relates to 4-(biphenyl-3-yl)-1H-pyrazolo[3,4-c]pyridazine derivatives of formula (I), and pharmaceutically acceptable salts thereof, wherein X, R1, R2, R3, R4 and R5 are as defined in the description. The pyrazolopyridazine derivatives of the present invention modulate the activity of the GABAA receptor. They may useful in the treatment of a number of conditions, including pain and epilepsy.

  本发明涉及吡唑吡啶并咪唑衍生物。更具体地，涉及公式（I）的4-（联苯基-3-基）-1H-吡唑并[3，4-c]咪唑衍生物及其药学上可接受的盐，其中X，R1，R2，R3，R4和R5如描述中所定义。本发明的吡唑吡啶衍生物调节GABAA受体的活性。它们可能在治疗许多疾病，包括疼痛和癫痫方面有用。
• IMIDAZOPYRIDAZINE DERIVATIVES AS GABAA RECEPTOR MODULATORS
  申请人：Pfizer Limited

  公开号：EP2938615B1

  公开（公告）日：2016-10-26
• IMIDAZOPYRIDAZINE DERIVATIVES AS MODULATORS OF THE GABAA RECEPTOR ACTIVITY.
  申请人：Pfizer Limited

  公开号：EP3154979A1

  公开（公告）日：2017-04-19