4-oxo-1,4-dihydroquinoline-3-carboxamide

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 4-oxo-1,4-dihydroquinoline-3-carboxamide
• 英文别名: 4-oxo-1H-quinoline-3-carboxamide
• 化学式: C₁₀H₈N₂O₂
• 分子量: 188.186
• InChiKey: CVAWACBLSANHSQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.2
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  72.2
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-oxo-1,4-dihydroquinoline-3-carboxamide 在 盐酸 作用下， 生成 4-氧代-1,4-二氢喹啉-3-羧酸
  参考文献：
  名称：

  v. Niementowski; Sucharda, Journal fur praktische Chemie (Leipzig 1954), 1916, vol. <2> 94, p. 225

  摘要：

  DOI：
• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 生成 4-oxo-1,4-dihydroquinoline-3-carboxamide
  参考文献：
  名称：

  v. Niementowski; Sucharda, Journal fur praktische Chemie (Leipzig 1954), 1916, vol. <2> 94, p. 225

  摘要：

  DOI：

文献信息

• Substituted quinolinecarboxamides as antiviral agents
  申请人：——

  公开号：US20020165253A1

  公开（公告）日：2002-11-07

  The present invention discloses disubstiuted 4-oxo-1,4-dihydro-3-quinolinecarboxamide derivatives. The compounds are useful as antiviral agents, in particular, as agents against viruses of the herpes family.

  本发明公开了二取代的4-氧代-1,4-二氢-3-喹啉羧酰胺衍生物。这些化合物可用作抗病毒剂，特别是用于抗击疱疹病毒家族的药剂。
• 4-oxo-1,4-dihydroquinoline-3-carboxamide as selective ligand for cannabinoid receptor 2 for diagnosis and therapy
  申请人：ETH Zurich

  公开号：EP2966062A1

  公开（公告）日：2016-01-13

  The present invention is directed to new compounds selectively binding the cannabinoid 2 receptor. In addition, the invention relates to the use of said compounds for determining cannabinoid receptor 2 (CB2)-selective receptor localization and density, preferably in the central nervous system (CNS), the peripheral nervous system (PNS), heart, liver, gastrointestinal tract, spleen, pancreas, kidney, testis, ovary and/or the prostate. Moreover, the invention pertains to the use of said compounds in the diagnosis, prophylaxis and/or therapy of CB2 receptor-related diseases.

  本发明涉及新化合物，其选择性地结合大麻素2受体。此外，该发明涉及利用所述化合物确定大麻素受体2（CB2）选择性受体的定位和密度，优选在中枢神经系统（CNS）、外周神经系统（PNS）、心脏、肝脏、胃肠道、脾脏、胰腺、肾脏、睾丸、卵巢和/或前列腺。此外，该发明涉及利用所述化合物在CB2受体相关疾病的诊断、预防和/或治疗中的应用。
• Multitarget Compounds Active at a PPAR and Cannabinoid Receptor
  申请人：Desreumaux Pierre

  公开号：US20110039808A1

  公开（公告）日：2011-02-17

  There is a need for pharmaceutical compounds which have activity at, at least one of a PPAR and a cannabinoid receptor. Thus there are provided such compounds, wherein the compound comprises: a PPAR pharmacophore and a cannabinoid pharmacophore linked together by a moiety comprising a fused bicyclic ring comprising a five membered ring fused with a six membered ring or a six membered ring fused with a six membered ring; wherein the cannabinoid pharmacophore comprises the fused bicyclic ring; and the PPAR pharmacophore comprises a salicylic acid, alkoxybenzylacetic acid or a alkoxyphenylacetic acid functionality; and wherein the PPAR pharmacophore is linked to the bicyclic ring of the cannabinoid pharmacophore through a linker comprising an amine or an amide functional group.

  需要具有至少一种PPAR和大麻受体活性的药物化合物。因此提供了这样的化合物，其中该化合物包括：由包含一个五元环与一个六元环或一个六元环与一个六元环融合的融合双环环的基团连接在一起的PPAR药效团和大麻药效团；其中大麻药效团包括融合双环环；而PPAR药效团包括水杨酸、烷氧基苯乙酸或烷氧基苯乙酸官能团；PPAR药效团通过包含胺基或酰胺官能团的连接物连接到大麻药效团的双环环上。
• 4-oxo-1,4-dihydro-3-cinnolinecarboxamides as antiviral agents
  申请人：——

  公开号：US20020045619A1

  公开（公告）日：2002-04-18

  This invention provides compounds of formula I; 1 which are useful as antiviral agents.

  这项发明提供了以下式I的化合物；1，这些化合物可用作抗病毒剂。
• 4-hydroxycinnoline-3-carboxyamides as antiviral agents
  申请人：——

  公开号：US20020042397A1

  公开（公告）日：2002-04-11

  Certain novel 4-hydroxycinnoline-3-carboxyamides. The compounds are particularly effective in the treatment or prevention of viral infections, particularly infections caused by herpes viruses including herpes simplex virus types 1 and 2, human herpes virus types 6, 7 and 8, varicello zoster virus, human cytomegalovirus or Epstein-Barr virus.

  某些新型4-羟基肉桂酰胺基喹啉化合物。这些化合物在治疗或预防病毒感染方面特别有效，尤其是对由疱疹病毒引起的感染，包括单纯疱疹病毒类型1和2、人类疱疹病毒类型6、7和8、水痘-带状疱疹病毒、人类巨细胞病毒或EB病毒感染。