Methyl 2-phenylpyrazolo[1,5-b]pyridazine-3-carboxylate | 781674-48-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: Methyl 2-phenylpyrazolo[1,5-b]pyridazine-3-carboxylate
• 英文别名: methyl 2-phenylpyrazolo[1,5-b]pyridazine-3-carboxylate
• CAS: 781674-48-4
• 化学式: C₁₄H₁₁N₃O₂
• 分子量: 253.26
• InChiKey: MBJKOYANQXMVBG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  56.5
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  Methyl 2-phenylpyrazolo[1,5-b]pyridazine-3-carboxylate 在 sodium hydroxide 作用下， 以 乙醇 为溶剂， 生成 2-Phenylpyrazolo[1,5-b]pyridazine-3-carboxylic acid
  参考文献：
  名称：

  Identification of 2,3-diaryl-pyrazolo[1,5-b]pyridazines as potent and selective cyclooxygenase-2 inhibitors

  摘要：

  GW406381 (8), currently undergoing clinical evaluation for the treatment of inflammatory pain is a member of a novel series of 2,3-diaryl-pyrazolo[1,5-b]pyridazine based cyclooxygenase-2 (COX-2) inhibitors, which have been shown to be highly potent and selective. Several examples of the series, in addition to possessing favourable pharmacokinetic profiles and analgesic activity in vivo, have also demonstrated relatively high brain penetration in the rat compared with the clinically available compounds, which may ultimately prove beneficial in the treatment of pain. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.07.089
• 作为产物：
  描述：

  苯丙炔酸甲酯 、 哒螨酮,1-氨基-碘(1∶1) 在 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 乙腈 为溶剂， 生成 Methyl 2-phenylpyrazolo[1,5-b]pyridazine-3-carboxylate
  参考文献：
  名称：

  Identification of 2,3-diaryl-pyrazolo[1,5-b]pyridazines as potent and selective cyclooxygenase-2 inhibitors

  摘要：

  GW406381 (8), currently undergoing clinical evaluation for the treatment of inflammatory pain is a member of a novel series of 2,3-diaryl-pyrazolo[1,5-b]pyridazine based cyclooxygenase-2 (COX-2) inhibitors, which have been shown to be highly potent and selective. Several examples of the series, in addition to possessing favourable pharmacokinetic profiles and analgesic activity in vivo, have also demonstrated relatively high brain penetration in the rat compared with the clinically available compounds, which may ultimately prove beneficial in the treatment of pain. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.07.089

文献信息

• Identification of 2,3-diaryl-pyrazolo[1,5-b]pyridazines as potent and selective cyclooxygenase-2 inhibitors
  作者：Paul Beswick、Sharon Bingham、Chas Bountra、Terry Brown、Kerry Browning、Ian Campbell、Iain Chessell、Nick Clayton、Sue Collins、John Corfield、Stephen Guntrip、Claudine Haslam、Paul Lambeth、Fiona Lucas、Neil Mathews、Graham Murkit、Alan Naylor、Neil Pegg、Elizabeth Pickup、Hazel Player、Helen Price、Alexander Stevens、Sharon Stratton、Joanne Wiseman

  DOI：10.1016/j.bmcl.2004.07.089

  日期：2004.11

  GW406381 (8), currently undergoing clinical evaluation for the treatment of inflammatory pain is a member of a novel series of 2,3-diaryl-pyrazolo[1,5-b]pyridazine based cyclooxygenase-2 (COX-2) inhibitors, which have been shown to be highly potent and selective. Several examples of the series, in addition to possessing favourable pharmacokinetic profiles and analgesic activity in vivo, have also demonstrated relatively high brain penetration in the rat compared with the clinically available compounds, which may ultimately prove beneficial in the treatment of pain. (C) 2004 Elsevier Ltd. All rights reserved.