4-methoxy-5-methyl-indan-1-one | 1033811-69-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 茚满类
• 英文名称: 4-methoxy-5-methyl-indan-1-one
• 英文别名: 4-methoxy-5-methyl-2,3-dihydroinden-1-one
• CAS: 1033811-69-6
• 化学式: C₁₁H₁₂O₂
• mdl: MFCD18647943
• 分子量: 176.215
• InChiKey: LZYXYCODHMBELL-UHFFFAOYSA-N

物化性质

• 沸点：
  321.9±41.0 °C(Predicted)
• 密度：
  1.134±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.363
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 危险性防范说明：
  P261,P264,P270,P271,P280,P301+P312,P302+P352,P304+P340,P305+P351+P338,P330,P332+P313,P337+P313,P362,P403+P233,P405,P501
• 危险性描述：
  H302,H315,H319,H335

反应信息

• 作为反应物：
  描述：

  4-methoxy-5-methyl-indan-1-one 在 氢溴酸 、 溴 、 溶剂黄146 作用下， 以44.2%的产率得到2-bromo-4-methoxy-5-methyl-indan-1-one
  参考文献：
  名称：

  Novel Compounds

  摘要：

  本发明公开了一种新型的甲状腺类似化合物，其化学式为（I），其中R1、R2、R3、R4和Z如规范中所定义，以及其制备方法、含有这种化合物的组合物和这种化合物及组合物作为药物的用途。此外，化合物的化学式（I）具有与甲状腺受体显著低的结合亲和力，因此在很大程度上缺乏甲状腺毒性作用。该发明还涉及将化学式（I）的化合物用于制备用于治疗肥胖、血脂异常、代谢综合征以及与代谢综合征相关的合并症等各种疾病状况的药物。

  公开号：

  US20100168110A1
• 作为产物：
  描述：

  8-methylcoumarin 在 palladium on activated carbon aluminum (III) chloride 、 氢气 、 potassium carbonate 作用下， 以 乙酸乙酯 、 N,N-二甲基甲酰胺 为溶剂， 180.0 ℃ 、1.72 MPa 条件下， 反应 23.0h， 生成 4-methoxy-5-methyl-indan-1-one
  参考文献：
  名称：

  WO2008/149379

  摘要：

  公开号：

文献信息

• SUBSTITUTED 2-AMINO-FUSED HETEROCYCLIC COMPOUNDS
  申请人：Huang Liming

  公开号：US20120035194A1

  公开（公告）日：2012-02-09

  The present invention relates to compounds of formula (I), or a pharmaceutically acceptable salt or solvate thereof, wherein: R 1 , R 2 , Z 1 , t, and ring A are as defined in the specification. The invention also relates to pharmaceutical compositions comprising the compounds of formula (I) and methods of treating a condition that is mediated by the modulation of JNK, such as diabetes, the method comprising administering to a mammal an effective amount of a compound of formula (I).

  本发明涉及公式（I）的化合物，或其药学上可接受的盐或溶剂，其中：R1、R2、Z1、t和环A的定义如规范中所述。本发明还涉及包含公式（I）化合物的制药组合物以及治疗通过调节JNK介导的疾病的方法，例如糖尿病，该方法包括向哺乳动物施用公式（I）化合物的有效量。
• NOVEL COMPOUNDS
  申请人：Chhipa Laxmikant

  公开号：US20120202816A1

  公开（公告）日：2012-08-09

  The present invention discloses a novel thyroid like compounds of formula (I), wherein R 1 R 2 , R 3 , R 4 and Z are as defined in the specification, method for its preparation, composition containing such compounds and use of such compounds and composition as medicament. Further, compounds of formula (I) has significantly low binding affinity to thyroid receptors and thus considerably devoid of thyrotoxic effects. The invention also relates to the use of the compound of formula (I) for the preparation of a medicament for treating various disease conditions such as obesity, dyslipidemia, metabolic syndrome and co-morbidities associated with metabolic syndrome.

  本发明揭示了一种新型的类甲状腺化合物，其化学式为（I），其中R1R2、R3、R4和Z的定义如规范中所述，以及其制备方法、含有该类化合物的组合物以及该类化合物和组合物作为药物的用途。此外，化合物（I）具有显著低的甲状腺受体结合亲和力，因此明显缺乏甲状腺毒性作用。本发明还涉及将化合物（I）用于制备治疗肥胖、血脂异常、代谢综合征和与代谢综合征相关的共病症的药物的用途。
• Thyroid like compounds
  申请人：Torrent Pharmaceuticals Ltd.

  公开号：US08143424B2

  公开（公告）日：2012-03-27

  A novel thyroid like compounds of formula (I), wherein R1, R2, R3, R4 and Z are as defined in the specification, method for its preparation, composition and use thereof. Further, compounds of formula (I) has significantly low binding affinity to thyroid receptors and thus considerably devoid of thyrotoxic effects. The invention also relates to the use of the compound of formula (I) for the preparation of a medicament for treating various disease conditions including obesity, dyslipidemia, metabolic syndrome and co-morbidities associated with metabolic syndrome.

  一种具有式（I）的新型甲状腺类似物，其中R1、R2、R3、R4和Z如规范中所定义，其制备方法、组合物和使用方法。此外，式（I）化合物与甲状腺受体的结合亲和力显著降低，因此极少具有甲状腺毒性作用。本发明还涉及使用式（I）化合物制备药物，用于治疗包括肥胖、血脂异常、代谢综合征以及与代谢综合征相关的共病症等各种疾病条件。
• Pyrazole-based thyroid receptor compounds
  申请人：Chhipa Laxmikant

  公开号：US08378118B2

  公开（公告）日：2013-02-19

  The present invention discloses a novel thyroid like compounds of formula (I), wherein R1 R2, R3, R4 and Z are as defined in the specification, method for its preparation, composition containing such compounds and use of such compounds and composition as medicament. Further, compounds of formula (I) has significantly low binding affinity to thyroid receptors and thus considerably devoid of thyrotoxic effects. The invention also relates to the use of the compound of formula (I) for the preparation of a medicament for treating various disease conditions such as obesity, dyslipidemia, metabolic syndrome and co-morbidities associated with metabolic syndrome.

  本发明揭示了一种新颖的甲状腺类似化合物，其化学式为（I），其中R1、R2、R3、R4和Z如规范中所定义，以及其制备方法、含有此类化合物的组合物和将此类化合物和组合物用作药物的用途。此外，化合物（I）对甲状腺受体的结合亲和力显著降低，因此在很大程度上缺乏甲状腺毒性效应。本发明还涉及将化合物（I）用于制备治疗肥胖症、血脂异常、代谢综合征以及与代谢综合征相关的共病症的药物。
• Novel 2-imidazoles as potent and selective α1A adrenoceptor partial agonists
  作者：Gavin A. Whitlock、Kelly Conlon、Gordon McMurray、Lee R. Roberts、Alan Stobie、Richard J. Thurlow

  DOI：10.1016/j.bmcl.2008.03.070

  日期：2008.5

  Novel 2-imidazoles have been identified as potent partial agonists of the alpha(1A) adrenergic receptor, with good selectivity over the alpha(1B), alpha(1D) and alpha(2A) receptor sub-types. Sulfonamide 23 possessed attractive drug-like properties with respect to physicochemical and ADME properties and wide ligand selectivity. (C) 2008 Elsevier Ltd. All rights reserved.