3-(2-氨基丙基)吲哚盐酸盐 | 879-36-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 中文名称: 3-(2-氨基丙基)吲哚盐酸盐
• 英文名称: alpha-Methyltryptamine hydrochloride
• 英文别名: 2-indol-3-yl-1-methyl-ethylamine; hydrochloride；2-Indol-3-yl-1-methyl-aethylamin; Hydrochlorid；1-(1H-indol-3-yl)propan-2-amine hydrochloride；1-(1H-indol-3-yl)propan-2-amine;hydrochloride
• CAS: 879-36-7
• 化学式: C₁₁H₁₄N₂*ClH
• 分子量: 210.706
• InChiKey: SNEXLQZZENRCSB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.48
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  43.4
• 氢给体数：
  2
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  6,8-dibromo-3-(prop-1-en-2-yl)imidazo[1,2-a]pyrazine 、 3-(2-氨基丙基)吲哚盐酸盐 在 N,N-二异丙基乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 6-bromo-N-[1-(1H-indol-3-yl)propan-2-yl]-3-prop-1-en-2-ylimidazo[1,2-a]pyrazin-8-amine
  参考文献：
  名称：

  [EN] COMPOUNDS AND METHODS FOR THE MODULATION OF AhR
  [FR] COMPOSÉS ET PROCÉDÉS POUR LA MODULATION D'AHR

  摘要：

  本文提供了化合物、组合物及使用这些化合物和组合物治疗部分受AhR调控的疾病的方法。这些化合物用以下式表示：（I），其中字母和符号a、b、c、d、e、f、A、R1、X1、Ar1和Ar2的含义在规范中提供。

  公开号：

  WO2019156989A1

文献信息

• Azepinoindole and pyridoindole derivatives as pharmaceutical agents
  申请人：X-Ceptor Therapeutics Inc.

  公开号：US20040023947A1

  公开（公告）日：2004-02-05

  Compounds, compositions and methods for modulating the activity of receptors are provided. In particular compounds and compositions are provided for modulating the activity of receptors and for the treatment, prevention, or amelioration of one or more symptoms of disease or disorder directly or indirectly related to the activity of the receptors.

  提供了调节受体活性的化合物、组合物和方法。特别提供了用于调节受体活性和治疗、预防或改善与受体活性直接或间接相关的一种或多种疾病或障碍症状的化合物和组合物。
• Azepinoindole and Pyridoindole Derivatives as Pharmaceutical Agents
  申请人：Martin Richard

  公开号：US20090326218A1

  公开（公告）日：2009-12-31

  Compounds, compositions and methods for modulating the activity of receptors are provided. In particular compounds and compositions are provided for modulating the activity of receptors and for the treatment, prevention, or amelioration of one or more symptoms of disease or disorder directly or indirectly related to the activity of the receptors.

  本发明提供了用于调节受体活性的化合物、组合物和方法。特别提供了用于调节受体活性的化合物和组合物，以及用于治疗、预防或缓解与受体活性直接或间接相关的一种或多种疾病或障碍的症状的方法。
• PESTICIDAL COMPOSITION COMPRISING INDOLE DERIVATES
  申请人：Bednarek Pawel

  公开号：US20090028796A1

  公开（公告）日：2009-01-29

  The present invention is directed to pesticidal compositions comprising indole derivatives. These indole derivatives are especially active against phytopathogenic fungi. Furthermore, the invention relates to the use of indole derivatives for the production of pesticides and the use of the compositions according to the invention as pesticides. The present invention is also directed to a process for producing a pesticidal composition and to pesticidal compositions prepared by this process. In addition, the invention relates to a process for preventing or combating pests and to a process for protecting plants against pests, especially against phytopathogenic fungi. Further, the invention is directed to plants or seeds as well as objects or materials which have been protected against pests by treatment with a composition according to the invention. Further, the invention is directed to a method for identifying a substance having pesticidal activity. Further, the invention is directed to a method of identifying the mode of action of and/or of providing binding proteins for a pesticidal compound of the present invention. Finally, the invention is directed to a method for diagnosing pest infection of a plant and to the use of a pesticidal compound of the present invention as diagnostic markers.

  本发明涉及包含吲哚衍生物的杀虫组合物。这些吲哚衍生物特别对植物病原真菌具有活性。此外，本发明涉及使用吲哚衍生物制备杀虫剂以及使用本发明中的组合物作为杀虫剂。本发明还涉及制备杀虫组合物的过程以及通过该过程制备的杀虫组合物。此外，本发明还涉及预防或对抗害虫的过程以及保护植物免受害虫，特别是植物病原真菌的过程。此外，本发明还涉及经过本发明中的组合物处理后受到保护的植物或种子以及物体或材料。本发明还涉及识别具有杀虫活性的物质的方法。此外，本发明还涉及识别本发明中杀虫化合物的作用方式和/或提供结合蛋白的方法。最后，本发明涉及诊断植物害虫感染的方法以及使用本发明中的杀虫化合物作为诊断标记的方法。
• Arylsubstituted piperazines useful in the treatment of benign prostatic hyperplasia
  申请人：——

  公开号：US20030220493A1

  公开（公告）日：2003-11-27

  This invention relates to a series of arylsubstituted piperazines, of Formula I 1 pharmaceutical compositions containing them and intermediates used in their manufacture. The compounds of the invention selectively inhibit binding to the &agr;-1a adrenergic receptor, a receptor which has been implicated in benign prostatic hyperplasia. As such the compounds are potentially useful in the treatment of this and other disease.

  本发明涉及一系列芳基取代的哌嗪类化合物，其式为 I 1 含有这些化合物的药物组合物以及用于制造这些化合物的中间体。本发明的化合物可选择性地抑制与&agr;-1a肾上腺素能受体的结合，该受体与良性前列腺增生症有关。因此，本发明化合物可用于治疗良性前列腺增生症和其他疾病。
• AZEPINOINDOLE AND PYRIDOINDOLE DERIVATIVES AS PHARMACEUTICAL AGENTS
  申请人：X-Ceptor Therapeutics, Inc.

  公开号：EP1532153B1

  公开（公告）日：2012-02-29