2-pyrrol-1-yl-3H-quinazolin-4-one | 37488-66-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: 2-pyrrol-1-yl-3H-quinazolin-4-one
• 英文别名: 2-pyrrol-1-yl-3H-quinazolin-4-one
• CAS: 37488-66-7
• 化学式: C₁₂H₉N₃O
• 分子量: 211.223
• InChiKey: ROXOUIWRDPIJRB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  16
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  46.4
• 氢给体数：
  1
• 氢受体数：
  1

文献信息

• HEPATITIS C SERINE PROTEASE INHIBITORS AND USES THEREFOR
  申请人：Campbell David Alan

  公开号：US20090325889A1

  公开（公告）日：2009-12-31

  The present invention provides novel compounds which mimic peptides with a C-terminal penultimate proline, such compounds being useful as protease inhibitors, particularly as inhibitors of serine proteases, and more particularly as inhibitors of the NS3 serine protease from hepatitis C. The compounds find utility as antiviral agents directed at hepatitis C. The invention further provides methods of employing such inhibitors, alone or in combination with other therapeutic agents, to treat hepatitis C infection in a subject in need of such treatment.

  本发明提供了一种新型化合物，其模拟具有C-末端次末端脯氨酸的肽，这些化合物可用作蛋白酶抑制剂，特别是丝氨酸蛋白酶的抑制剂，更特别地，作为丙型肝炎NS3丝氨酸蛋白酶的抑制剂。这些化合物可用作针对丙型肝炎的抗病毒剂。本发明还提供了使用这些抑制剂的方法，单独或与其他治疗剂联合使用，用于治疗需要此类治疗的患者的丙型肝炎感染。
• [EN] HEPATITIS C SERINE PROTEASE INHIBITORS AND USES THEREFOR<br/>[FR] INHIBITEURS DE LA SÉRINE PROTÉASE DE L'HÉPATITE C ET EMPLOI DESDITS INHIBITEURS
  申请人：PHENOMIX CORP

  公开号：WO2007016476A2

  公开（公告）日：2007-02-08

  [EN] The present invention provides novel compounds which mimic peptides with a C-terminal penultimate proline, such compounds being useful as protease inhibitors, particularly as inhibitors of serine proteases, and more particularly as inhibitors of the NS3 serine protease from hepatitis C. The compounds find utility as antiviral agents directed at hepatitis C. The invention further provides methods of employing such inhibitors, alone or in combination with other therapeutic agents, to treat hepatitis C infection in a subject in need of such treatment.
  [FR] La présente invention concerne de nouveaux composés qui imitent des peptides comportant une proline en avant-dernière position au niveau de l'extrémité C, de tels composés pouvant être employés en tant qu'inhibiteurs de protéase, en particulier en tant qu'inhibiteurs de sérine protéases, et plus particulièrement en tant qu'inhibiteurs de la sérine protéase NS3 de l'hépatite C. Les composés peuvent être employés en tant qu'agents antiviraux contre l'hépatite C. L'invention concerne en outre des méthodes d'emploi de tels inhibiteurs, seuls ou combinés à d'autres agents thérapeutiques, pour traiter une infection par l'hépatite C chez un sujet nécessitant un tel traitement.
• [EN] SUBSTITUTED FUSED PYRIMIDINONE COMPOUNDS<br/>[FR] COMPOSÉS DE PYRIMIDINONE FUSIONNÉS SUBSTITUÉS
  申请人：TORRENT PHARMACEUTICALS LTD

  公开号：WO2017187324A1

  公开（公告）日：2017-11-02

  Provided herein are novel fused pyrimidinone derivatives of Formula (I) and synthetic intermediates that are useful in preparing the compounds of formula (I). Further provided herein is a method for preparation of a compound of formula (I) or intermediates, a pharmaceutical composition comprising a compound of formula (I), and use of a compound of formula (I).