5-(trifluoromethyl)pyrazolo[1,5-a]pyridine-3-carbaldehyde | 1101119-94-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡唑并吡啶类
• 英文名称: 5-(trifluoromethyl)pyrazolo[1,5-a]pyridine-3-carbaldehyde
• CAS: 1101119-94-1
• 化学式: C₉H₅F₃N₂O
• 分子量: 214.147
• InChiKey: WHOLGEZFOJMJQZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  34.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  5-(trifluoromethyl)pyrazolo[1,5-a]pyridine-3-carbaldehyde 在 碳酸氢钠 作用下， 以 甲醇 为溶剂， 反应 0.5h， 生成 N,2-dimethyl-5-nitro-N'-((5-(trifluoromethyl)pyrazolo[1,5-a]pyridin-3-yl)methylene)benzenesulfonohydrazide
  参考文献：
  名称：

  Discovery of pyrazolo[1,5-a]pyridines as p110α-selective PI3 kinase inhibitors

  摘要：

  We have made a novel series of pyrazolo[1,5-a]pyridines as PI3 kinase inhibitors, and demonstrated their selectivity for the p110 alpha isoform over the other Class Ia PI3 kinases. We investigated the SAR around the pyrazolo[1,5-a] pyridine ring system, and found compound 5x to be a particularly potent example (p110 alpha IC50 0.9 nM). This compound inhibits cell proliferation and phosphorylation of Akt/PKB, a downstream marker of PI3 kinase activity, and showed in vivo activity in an HCT-116 human xenograft model. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.11.029
• 作为产物：
  描述：

  4-三氟甲基吡啶 在 manganese(IV) oxide 、 lithium aluminium tetrahydride 、 2,4,6-三甲基苯磺酰羟胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 117.0h， 生成 5-(trifluoromethyl)pyrazolo[1,5-a]pyridine-3-carbaldehyde
  参考文献：
  名称：

  Discovery of pyrazolo[1,5-a]pyridines as p110α-selective PI3 kinase inhibitors

  摘要：

  We have made a novel series of pyrazolo[1,5-a]pyridines as PI3 kinase inhibitors, and demonstrated their selectivity for the p110 alpha isoform over the other Class Ia PI3 kinases. We investigated the SAR around the pyrazolo[1,5-a] pyridine ring system, and found compound 5x to be a particularly potent example (p110 alpha IC50 0.9 nM). This compound inhibits cell proliferation and phosphorylation of Akt/PKB, a downstream marker of PI3 kinase activity, and showed in vivo activity in an HCT-116 human xenograft model. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2011.11.029

文献信息

• [EN] PYRAZOLO[1,5-A]PYRIDINES AND THEIR USE IN CANCER THERAPY<br/>[FR] PYRAZOLO[1,5-A]PYRIDINES ET LEUR UTILISATION EN CANCÉROTHÉRAPIE
  申请人：AUCKLAND UNISERVICES LTD

  公开号：WO2009008748A1

  公开（公告）日：2009-01-15

  Pyrazolo[1,5-a]pyridines are described, including methods for their preparation, and their use as agents or drugs for cancer therapy, both alone or in combination with radiation and/or other anticancer drugs.

  Pyrazolo[1,5-a]吡啶类化合物被描述，包括它们的制备方法，以及它们作为抗癌治疗药物或药剂的用途，无论是单独使用还是与放疗和/或其他抗癌药物联合使用。
• PYRAZOLO[1,5-a]PYRIDINES AND THEIR USE IN CANCER THERAPY
  申请人：Kendall Jackie Diane

  公开号：US20100226881A1

  公开（公告）日：2010-09-09

  Pyrazolo[1,5-a]pyridines are described, including methods for their preparation, and their use as agents or drugs for cancer therapy, both alone or in combination with radiation and/or other anticancer drugs.

  本文描述了Pyrazolo[1,5-a]pyridines，包括其制备方法，以及其作为单独或与放射治疗和/或其他抗癌药物联合使用的癌症治疗药物或代理。
• PYRAZOLO[1,5-A]PYRIDINES AND THEIR USE IN CANCER THERAPY
  申请人：AUCKLAND UNISERVICES LIMITED

  公开号：EP2176260A1

  公开（公告）日：2010-04-21