5-[(7-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methyl]-1H-imidazole

• 分子结构分类: 有机化合物 - 苯类化合物 - 四氢化萘
• 英文名称: 5-[(7-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methyl]-1H-imidazole
• 化学式: C₁₅H₁₈N₂O
• 分子量: 242.321
• InChiKey: CBMIGXRVXBNVRL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  37.9
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  7-甲氧基-1-萘满酮 在 palladium on activated charcoal 氢氧化钾 、 硫酸 、 氢气 、 一水合肼 作用下， 以 甲醇 、 二乙二醇 为溶剂， 25.0~195.0 ℃ 、100.0 kPa 条件下， 反应 27.5h， 生成 5-[(7-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methyl]-1H-imidazole
  参考文献：
  名称：

  作为 P450 芳香族、P450 17 和 P450 TxA2 抑制剂的唑取代四氢萘的合成和评价

  摘要：

  寻找用于治疗雌激素和雄激素依赖性癌症以及预防转移的潜在药物、四氢萘酮、四氢萘和在苯核上带有 OCH3 取代基和咪唑 - 4 - 基、咪唑 - 1- 的二氢萘基或 1,2,4-三唑-1-基取代基在 2-位合成，在环之间有和没有 C1-间隔物（化合物 2-26）。在体外测试了这些化合物对三种靶酶 P450 arom（人胎盘微粒体）、P450 17（大鼠睾丸微粒体）和 P450 TxA2（柠檬酸化人全血）的抑制作用。为了检查选择性，在体外进一步测试了一些化合物对 P450 18（牛肾上腺线粒体）、P450 see（牛肾上腺线粒体）和皮质激素形成（醛固酮、皮质酮；ACTH 刺激的大鼠肾上腺组织）的抑制。体内，

  DOI：

  10.1002/ardp.19963290506

文献信息

• IMIDIAZOLE DERIVATIVES AND THEIR USE AS AGONISTS SELECTIVE AT ALPHA 2B OR 2B/2C ADRENERGIC RECEPTORS
  申请人：ALLERGAN, INC.

  公开号：EP1370533B1

  公开（公告）日：2015-05-06
• ALPHA-2B RECEPTOR AGONIST AND 5HT4 SEROTONIN RECEPTOR COMPOSITIONS FOR TREATING GASTROINTESTINAL MOTILITY DISORDERS
  申请人：Brooks Gregory F.

  公开号：US20080153825A1

  公开（公告）日：2008-06-26

  Disclosed herein is a pharmaceutical composition comprising a 5-HT4 serotonin receptor agonist and an alpha-2B receptor agonist. The composition is effective for treating gastrointestinal motility disorders, and methods of treating such disorders using the composition and compounds comprising it are also disclosed.
• ALPHA-2B RECEPTOR AGONIST AND ANTICONVULSANT COMPOSITIONS FOR TREATING CHRONIC PAIN
  申请人：Gil Daniel W.

  公开号：US20080153874A1

  公开（公告）日：2008-06-26

  Disclosed herein is a pharmaceutical composition comprising a pain-relieving anticonvulsant and an alpha-2B receptor agonist. The composition is effective for treating chronic pain, and methods of treating chronic pain using the composition and the compounds comprising it are also disclosed.
• ALPHA-2B RECEPTOR AGONIST AND ACID REDUCER COMPOSITIONS FOR TREATING GASTROINTESTINAL MOTILITY DISORDERS
  申请人：Brooks Gregory F.

  公开号：US20080153881A1

  公开（公告）日：2008-06-26

  Disclosed herein is a pharmaceutical composition comprising an acid reducer and an alpha-2B receptor agonist. The composition is effective for treating gastrointestinal motility disorders, and methods of treating such disorders using the composition and compounds comprising it are also disclosed.
• ALPHA-2B RECEPTOR AGONIST AND RELAXANT COMPOSITIONS FOR TREATING GASTROINTESTINAL MOTILITY DISORDERS
  申请人：Brooks Gregory F.

  公开号：US20080153927A1

  公开（公告）日：2008-06-26

  Disclosed herein is a pharmaceutical composition comprising a relaxant and an alpha-2B receptor agonist. The composition is effective for treating gastrointestinal motility disorders, and methods of treating such disorders using the composition and compounds comprising it are also disclosed.