3-<2-(2,2,2-Trifluor-ethylamino)-propyl>-indol | 4822-07-5

• 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
• 英文名称: 3-<2-(2,2,2-Trifluor-ethylamino)-propyl>-indol
• 英文别名: 1-(1H-indol-3-yl)-N-(2,2,2-trifluoroethyl)propan-2-amine
• CAS: 4822-07-5
• 化学式: C₁₃H₁₅F₃N₂
• 分子量: 256.271
• InChiKey: ZGLNHSCSGHYBCC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  27.8
• 氢给体数：
  2
• 氢受体数：
  4

文献信息

• Compounds and Their Use in Treating Cancer
  申请人：AstraZeneca AB

  公开号：US20190194190A1

  公开（公告）日：2019-06-27

  The specification generally relates to compounds of Formula (I): and pharmaceutically acceptable salts and prodrugs thereof, where R 1 , R 4 , R 5 , R 6 , R 7 , Linker, X, Y, A, G, D and E have any of the meanings defined herein. This specification also relates to the use of such compounds and pharmaceutically acceptable salts and prodrugs thereof in methods of treatment of the human or animal body, for example in prevention or treatment of cancer. This specification also relates to processes and intermediate compounds involved in the preparation of such compounds and to pharmaceutical compositions containing them.

  本说明书一般涉及公式(I)的化合物： 以及药学上可接受的盐和前药，其中R1、R4、R5、R6、R7、Linker、X、Y、A、G、D和E具有此处定义的任何含义。本说明书还涉及将此类化合物以及药学上可接受的盐和前药用于治疗人体或动物体的方法，例如用于预防或治疗癌症。本说明书还涉及制备此类化合物涉及的工艺和中间化合物，以及含有它们的药物组合物。
• [EN] ESTROGEN RECEPTOR MODULATORS<br/>[FR] MODULATEURS DU RÉCEPTEUR DES ŒSTROGÈNES
  申请人：ASTRAZENECA AB

  公开号：WO2018138303A1

  公开（公告）日：2018-08-02

  The specification relates to compounds of Formula (I): (I) 5and to pharmaceutically acceptable salts thereof, to processes and intermediates used for their preparation, to pharmaceutical compositions containing them and to their use in the treatment of cell proliferative disorders.

  该规范涉及到式(I)的化合物，以及其药用盐，用于其制备的工艺和中间体，含有它们的药物组合物，以及它们在治疗细胞增殖性疾病中的用途。
• [EN] TETRAHYDRO-PYRIDO[3,4-b]INDOLE ESTROGEN RECEPTOR MODULATORS AND USES THEREOF<br/>[FR] MODULATEURS DES RÉCEPTEURS DES OESTROGÈNES TÉTRAHYDRO-PYRIDO[3,4-B]INDOLE ET UTILISATIONS ASSOCIÉES
  申请人：HOFFMANN LA ROCHE

  公开号：WO2016097072A1

  公开（公告）日：2016-06-23

  Described herein are tetrahydro-pyrido[3,4-b]indol-1-yl compounds with estrogen receptor modulation activity or function having the Formula (I) structure and stereoisomers, tautomers, or pharmaceutically acceptable salts thereof, and with the substituents and structural features described herein. Also described are pharmaceutical compositions and medicaments that include the Formula (I) compounds, as well as methods of using such estrogen receptor modulators, alone and in combination with other therapeutic agents, for treating diseases or conditions that are mediated or dependent upon estrogen receptors.

  本文描述了具有雌激素受体调节活性或功能的四氢吡啶并[3,4-b]吲哚-1-基化合物，其具有式（I）结构及其立体异构体、互变异构体或药学上可接受的盐，并具有所述的取代基和结构特征。还描述了包括式（I）化合物的药物组合物和药物，以及使用这种雌激素受体调节剂的方法，单独或与其他治疗剂联合治疗依赖于雌激素受体介导或依赖的疾病或病况。
• TETRAHYDRO-PYRIDO[3,4-b]INDOLE ESTROGEN RECEPTOR MODULATORS AND USES THEREOF
  申请人：Genentech, Inc.

  公开号：US20160175289A1

  公开（公告）日：2016-06-23

  Described herein are tetrahydro-pyrido[3,4-b]indol-1-yl compounds with estrogen receptor modulation activity or function having the Formula I structure: and stereoisomers, tautomers, or pharmaceutically acceptable salts thereof, and with the substituents and structural features described herein. Also described are pharmaceutical compositions and medicaments that include the Formula I compounds, as well as methods of using such estrogen receptor modulators, alone and in combination with other therapeutic agents, for treating diseases or conditions that are mediated or dependent upon estrogen receptors.

  本文描述了具有雌激素受体调节活性或功能的四氢-吡啶并[3,4-b]吲哚-1-基化合物，其具有I式结构：以及其立体异构体，互变异构体或药学上可接受的盐，以及所述取代基和结构特征。还描述了包括I式化合物的药物组合物和药物，以及使用这样的雌激素受体调节剂的方法，单独或与其他治疗剂联合治疗介导或依赖于雌激素受体的疾病或病况。
• TETRAHYDRO-PYRIDO[3,4-B]INDOLE ESTROGEN RECEPTOR MODULATORS AND USES THEREOF
  申请人：F. Hoffmann-La Roche AG

  公开号：EP3760623A1

  公开（公告）日：2021-01-06

  Described herein are tetrahydro-pyrido[3,4-b]indol-1-yl compounds with estrogen receptor modulation activity or function having the Formula I structure: and stereoisomers, tautomers, or pharmaceutically acceptable salts thereof, and with the substituents and structural features described herein. Also described are pharmaceutical compositions and medicaments that include the Formula I compounds, as well as methods of using such estrogen receptor modulators, alone and in combination with other therapeutic agents, for treating diseases or conditions that are mediated or dependent upon estrogen receptors.

  本文描述的是具有雌激素受体调节活性或功能的四氢吡啶并[3,4-b]吲哚-1-基化合物，其结构如式 I 所示： 及其立体异构体、同系物或药学上可接受的盐，并具有本文所述的取代基和结构特征。还描述了包括式 I 化合物的药物组合物和药物，以及单独或与其它治疗剂联合使用此类雌激素受体调节剂治疗介导或依赖于雌激素受体的疾病或病症的方法。