methyl 2-(3-pyridinyl)-1H-benzimidazole-5-carboxylate | 666181-01-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并咪唑类
• 英文名称: methyl 2-(3-pyridinyl)-1H-benzimidazole-5-carboxylate
• 英文别名: methyl 2-pyridin-3-yl-3H-benzimidazole-5-carboxylate
• CAS: 666181-01-7
• 化学式: C₁₄H₁₁N₃O₂
• 分子量: 253.26
• InChiKey: RGNPZGMDQFSNCZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 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：
  67.9
• 氢给体数：
  1
• 氢受体数：
  4

文献信息

• [EN] BENZIMIDAZOL DERIVATIVES FOR TREATING FILOVIRUS INFECTION<br/>[FR] DÉRIVÉS DE BENZIMIDAZOLE POUR LE TRAITEMENT D'UNE INFECTION PAR FILOVIRUS
  申请人：CENTRE NAT RECH SCIENT

  公开号：WO2018050771A1

  公开（公告）日：2018-03-22

  The present invention relates to compounds comprising a benzimidazole scaffold, and the use of such compounds for the treatment of viral diseases. The invention also relates to pharmaceutical compositions comprising said compounds as an active ingredient. In particular the compounds of the invention comprising a benzimidazole scaffold are used for the treatment of filoviruses or retroviruses, and preferably for the treatment of Ebola virus or HIV virus.

  本发明涉及含有苯并咪唑骨架的化合物，以及利用这些化合物治疗病毒性疾病。该发明还涉及包含上述化合物作为活性成分的药物组合物。特别是，本发明涉及含有苯并咪唑骨架的化合物用于治疗丝状病毒或逆转录病毒，尤其是用于治疗埃博拉病毒或艾滋病毒。
• [EN] NOVEL CHEMICAL COMPOUNDS<br/>[FR] NOUVEAUX COMPOSES CHIMIQUES
  申请人：SMITHKLINE BEECHAM CORP

  公开号：WO2005082901A1

  公开（公告）日：2005-09-09

  This invention relates to newly identified compounds for inhibiting hYAK3 proteins and methods for treating diseases associated with the imbalance or inappropriate activity of hYAK3 proteins.

  这项发明涉及新识别的化合物，用于抑制hYAK3蛋白，并用于治疗与hYAK3蛋白不平衡或不适当活性相关的疾病的方法。
• Novel Chemical Compounds
  申请人：Duffy J. Kevin

  公开号：US20070249599A1

  公开（公告）日：2007-10-25

  This invention relates to the newly identified compounds for inhibiting hYAK3 proteins and methods for treating diseases associated with the imbalance or inappropriate activity of hYAK3 proteins.

  本发明涉及一种新鉴定的化合物，用于抑制hYAK3蛋白质并治疗与hYAK3蛋白质不平衡或不适当活性相关的疾病的方法。
• THIAZOLONES FOR USE AS PI3 KINASE INHIBITORS
  申请人：Dhanak Dashyant

  公开号：US20090048252A1

  公开（公告）日：2009-02-19

  Invented is a method of inhibiting the activity/function of PI3 kinases using substituted thiazolones. Also invented is a method of treating one or more disease states selected from: autoimmune disorders, inflammatory diseases, cardiovascular diseases, neurodegenerative diseases, allergy, asthma, pancreatitis, multiorgan failure, kidney diseases, platelet aggregation, cancer, sperm motility, transplantation rejection, graft rejection and lung injuries by the administration of substituted thiazolones.

  本发明涉及使用取代噻唑酮抑制PI3激酶活性/功能的方法。同时本发明涉及使用取代噻唑酮治疗以下一种或多种疾病状态的方法：自身免疫性疾病、炎症性疾病、心血管疾病、神经退行性疾病、过敏、哮喘、胰腺炎、多器官衰竭、肾脏疾病、血小板聚集、癌症、精子活动力低下、移植排斥、移植物排斥和肺损伤。
• BENZIMIDAZOL DERIVATIVES FOR TREATING FILOVIRUS INFECTION
  申请人：CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE

  公开号：EP3296297A1

  公开（公告）日：2018-03-21

  The present invention relates to compounds comprising a benzimidazole scaffold, and the use of such compounds for the treatment of viral diseases. The invention also relates to pharmaceutical compositions comprising said compounds as an active ingredient. In particular the compounds of the invention comprising a benzimidazole scaffold are used for the treatment of filoviruses or retroviruses, and preferably for the treatment of Ebola virus or HIV virus.

  本发明涉及包含苯并咪唑支架的化合物，以及使用此类化合物治疗病毒性疾病。本发明还涉及包含上述化合物作为活性成分的药物组合物。 特别是包含苯并咪唑支架的本发明化合物可用于治疗丝状病毒或逆转录病毒，最好用于治疗埃博拉病毒或艾滋病毒。