9-[4-(3-carboxymethoxypropyl)(methyl)aminomethylbenzyl]-7,8-dihydro-2-(2-methoxyethoxy)-8-oxoadenine | 930293-86-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并嘧啶类
• 英文名称: 9-[4-(3-carboxymethoxypropyl)(methyl)aminomethylbenzyl]-7,8-dihydro-2-(2-methoxyethoxy)-8-oxoadenine
• 英文别名: 2-[3-[[4-[[6-amino-2-(2-methoxyethoxy)-8-oxo-7H-purin-9-yl]methyl]phenyl]methyl-methylamino]propoxy]acetic acid
• CAS: 930293-86-0
• 化学式: C₂₂H₃₀N₆O₆
• 分子量: 474.517
• InChiKey: OIFLGMJPEWLYNR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -2
• 重原子数：
  34
• 可旋转键数：
  14
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  152
• 氢给体数：
  3
• 氢受体数：
  10

文献信息

• [EN] AMINOQUINOLINE DERIVATIVES AS ANTIVIRAL AGENTS<br/>[FR] DÉRIVÉS D'AMINOQUINOLÉINE COMME AGENTS ANTIVIRAUX
  申请人：GLAXOSMITHKLINE LLC

  公开号：WO2012037108A1

  公开（公告）日：2012-03-22

  Provided are compounds of Formula (I) and Formula (II) and pharmaceutically acceptable salts thereof, their pharmaceutical compositions, their methods of preparation, and their use for treating viral infections mediated by a member of the Flaviviridae family of viruses such as hepatitis C virus (HCV).

  提供的是式(I)和式(II)的化合物及其药用盐，它们的药物组合物，它们的制备方法，以及它们用于治疗由黄病毒科病毒介导的病毒感染，如丙型肝炎病毒（HCV）。
• Benzazepine derivatives as histamine h3 antagonists
  申请人：Bailey Nicholas

  公开号：US20070060566A1

  公开（公告）日：2007-03-15

  The present invention relates to novel benzazepine derivatives of structure (I) having pharmacological activity, processes for their preparation, to compositions containing them and to their use in the treatment of neurological and psychiatric disorders. These compounds act as histamine H3 antagonists.

  本发明涉及具有药理活性的新型苯并氮杂环衍生物(I)的结构，其制备过程，包含它们的组合物以及它们在神经和精神障碍治疗中的应用。这些化合物作为组胺H3拮抗剂。
• NOVEL ADENINE COMPOUND
  申请人：Isobe Yoshiaki

  公开号：US20090105212A1

  公开（公告）日：2009-04-23

  A novel adenine compound represented by the formula (1): wherein A represents an (un)substituted aromatic carbocycle or (un)substituted aromatic heterocycle; L 1 , L 2 , and L 3 each independently represents linear or branched alkylene, etc.; R 1 represents (un)substituted alkyl, (un)substituted aryl, etc.; R 2 represents hydrogen or (un) substituted alkyl; R 3 represents (un)substituted alkyl, etc., provided that R 3 may be bonded to L 2 or L 3 to form a nitrogenous saturated heterocycle; and X represents oxygen, etc.; or a pharmaceutically acceptable salt of the compound. The compound and salt are useful as a medicine.

  一种新型腺嘌呤类化合物，其化学式为（1）：其中A代表（未）取代芳香族碳环或（未）取代芳香族杂环；L1，L2和L3分别独立地代表线性或支链烷基等；R1代表（未）取代烷基，（未）取代芳基等；R2代表氢或（未）取代烷基；R3代表（未）取代烷基等，但R3可与L2或L3结合形成含氮饱和杂环；X代表氧等；或该化合物的药学上可接受的盐。该化合物和盐作为药物有用。
• COMPOUNDS
  申请人：MITCHELL Darren Jason

  公开号：US20090192160A1

  公开（公告）日：2009-07-30

  The invention relates to compounds of formula (I) processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of conditions or disorders which are mediated via the GPR38 receptor.

  本发明涉及公式（I）化合物，其制备方法，包含它们的药物组合物以及它们在治疗通过GPR38受体介导的疾病或疾病的用途。
• Activator of TREK (TWIK RElated K+ channels) channels
  申请人：ONO PHARMACEUTICAL CO., LTD.

  公开号：US11046683B2

  公开（公告）日：2021-06-29

  Disclosed is a compound of formula (I): wherein all symbols are defined in the description. Also disclosed are pharmaceutical compositions comprising the compounds, methods of making the compounds, kits comprising the compounds, and methods of using the compounds, compositions and kits for treatment of disorders associated with TREK-1, TREK-2 or both TREK-1 and TREK-2 dysfunction in a mammal.

  本发明公开了一种式 (I) 的化合物： 其中所有符号在描述中定义。还公开了包含所述化合物的药物组合物、制造所述化合物的方法、包含所述化合物的试剂盒，以及使用所述化合物、组合物和试剂盒治疗哺乳动物中与 TREK-1、TREK-2 或 TREK-1 和 TREK-2 功能障碍相关的疾病的方法。