[1-(7,8-dimethoxy-4,10-dioxo-5H-triazolo[4,5-c][1]benzazepin-2-yl)-2-methylpropyl] 2-(2-methoxyethoxy)ethyl carbonate

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯氮卓类
• 英文名称: [1-(7,8-dimethoxy-4,10-dioxo-5H-triazolo[4,5-c][1]benzazepin-2-yl)-2-methylpropyl] 2-(2-methoxyethoxy)ethyl carbonate
• 化学式: C₂₂H₂₈N₄O₉
• 分子量: 492.5
• InChiKey: HQPULRWUWOPVGA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  35
• 可旋转键数：
  13
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  149
• 氢给体数：
  1
• 氢受体数：
  11

文献信息

• Tricyclic triazolobenzazepine derivatives, process for producing the same, and antiallergic agents
  申请人：Ohtsuka Yasuo

  公开号：US20060074074A1

  公开（公告）日：2006-04-06

  Tricyclic triazolobenzazepine derivatives in the form or a prodrug are provided. The compounds according to the present invention are those represented by formula (I) and pharmacologically acceptable salts and solvates thereon. The compounds are useful as antiallergic agents and exhibit excellent bioavailability. wherein R 1 represents hydrogen, OH, alkyl or phenyl alkyl, R 2 , R 3 , R 4 , and R 5 represent hydrogen, halogen, optionally protected hydroxyl, formyl, optionally substituted alkyl, alkenyl, alkoxy or the like, and Q represents a group selected from the following groups (i) to (iv), halogen, or alkoxy:

  本发明提供了三环三唑苯并氮杂蒽衍生物的前药形式。根据本发明，所述化合物为公式（I）所表示的化合物及其药理学上可接受的盐和溶剂化物。该化合物可用作抗过敏药物，且具有优异的生物利用度。其中R1代表氢、OH、烷基或苯基烷基，R2、R3、R4和R5代表氢、卤素、可选保护的羟基、甲酰基、可选取代的烷基、烯基、烷氧基或类似基团，Q代表以下基团（i）至（iv）、卤素或烷氧基中的一种。
• TRICYCLIC TRIAZOLOBENZAZEPINE DERIVATIVES, PROCESS FOR PRODUCING THE SAME, AND ANTIALLERGIC
  申请人：Meiji Seika Kaisha, Ltd.

  公开号：EP1026167A1

  公开（公告）日：2000-08-09

  Tricyclic triazolobenzazepine derivatives in the form of a prodrug are provided. The compounds according to the present invention are those represented by formula (I) and pharmacologically acceptable salts and solvates thereof. The compounds are useful as antiallergic agents and exhibit excellent bioavailability. wherein R1 represents hydrogen, OH, alkyl or phenyl alkyl, R2, R3, R4, and R5 represent hydrogen, halogen, optionally protected hydroxyl, formyl, optionally substituted alkyl, alkenyl, alkoxy or the like, and Q represents a group selected from the following groups (i) to (iv), halogen, or alkoxy:

  本发明提供了原药形式的三环三唑并氮杂卓衍生物。根据本发明的化合物是由式（I）代表的化合物及其药理学上可接受的盐和溶液。这些化合物可用作抗过敏剂，并具有良好的生物利用度。 其中 R1 代表氢、OH、烷基或苯基烷基、 R2、R3、R4 和 R5 代表氢、卤素、任选保护的羟基、甲酰基、任选取代的烷基、烯基、烷氧基或类似物，以及 Q 代表选自以下基团 (i) 至 (iv)、卤素或烷氧基：
• US7238812B2
  申请人：——

  公开号：US7238812B2

  公开（公告）日：2007-07-03