5,6-diisopropylindoline | 122299-60-9

• 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: 5,6-diisopropylindoline
• 英文别名: 5,6-Di(propan-2-yl)-2,3-dihydro-1H-indole
• CAS: 122299-60-9
• 化学式: C₁₄H₂₁N
• 分子量: 203.327
• InChiKey: RPBHKTPWEBEIDH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  12
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  吲哚啉 、 4,6-diisopropylindoline 、 5,6-diisopropylindoline 生成 2,3-二氢-6-(1-甲基乙基)-1H-吲哚(9ci)
  参考文献：
  名称：

  CHEXUTA, V. G.;KACHURIN, O. I.;OXRIMENKO, Z. A.;SHVETSOVA, T. I.

  摘要：

  DOI：
• 作为产物：
  描述：

  2,3-二氢-5-(1-甲基乙基)-1H-吲哚(9ci) 、 异丙醇 在 硫酸 作用下， 生成 5,6-diisopropylindoline
  参考文献：
  名称：

  Isopropylation of indoline

  摘要：

  DOI：

  10.1007/bf00476202

文献信息

• HUMAN IMMUNODEFICIENCY VIRUS PROTEASE INHIBITORS
  申请人：Ganguly A.K.

  公开号：US20110112068A1

  公开（公告）日：2011-05-12

  The described invention relates to novel human immunodeficiency virus protease inhibitors, pharmaceutical compositions containing at least one such inhibitor, methods of preparing such inhibitors, and methods of utilizing such inhibitors to treat HIV and HIV-related disorders.

  所描述的发明涉及新型人类免疫缺陷病毒蛋白酶抑制剂，包含至少一种此类抑制剂的药物组合物，制备此类抑制剂的方法，以及利用此类抑制剂治疗艾滋病毒及艾滋病毒相关疾病的方法。
• Nitrogen-containing heterocycle derivatives, pharmaceutical compositions, and methods of use thereof as antiviral agents
  申请人：Mjalli M.M. Adnan

  公开号：US20070219239A1

  公开（公告）日：2007-09-20

  The present application provides nitrogen-containing heterocycle derivatives that are antiviral compounds that may be useful in the treatment of a viral infection. Compounds of Formula (I) and pharmaceutical compositions comprising a compound of Formula (I) may be administered to a subject for antiviral therapy or prophylaxis.

  本申请提供了含氮杂环衍生物，这些衍生物是抗病毒化合物，可能在治疗病毒感染方面有用。具有式（I）的化合物和包含式（I）化合物的药物组合物可用于向受试者施行抗病毒治疗或预防。
• Aryl and heteroaryl compounds, compositions, methods of use
  申请人：Mjalli M.M. Adnan

  公开号：US20050171148A1

  公开（公告）日：2005-08-04

  This invention provides aryl and heteroaryl compounds, methods of their preparation, pharmaceutical compositions comprising the compounds, and their use in treating human or animal disorders. The compounds of the invention may be useful as antagonists, or partial antagonist of factor IX and/or factor XI and thus, may be used to inhibit the intrinsic pathway of blood coagulation. The compounds may be useful in a variety of applications including the management, treatment and/or control of diseases caused in part by the intrinsic clotting pathway utilizing factor IX and/or XI.

  这项发明提供了芳基和杂环芳基化合物，以及它们的制备方法、包含这些化合物的药物组合物，以及它们在治疗人类或动物疾病中的应用。该发明的化合物可能用作因子IX和/或因子XI的拮抗剂或部分拮抗剂，因此可以用于抑制血液凝固的内在途径。这些化合物可能在多种应用中有用，包括利用因子IX和/或XI的内在凝血途径部分引起的疾病的管理、治疗和/或控制。
• PYRIDO [5, 4-D] PYRIMIDINES AS CELL PROLIFERATION INHIBITORS
  申请人：Mantoulidis Andreas

  公开号：US20120094975A1

  公开（公告）日：2012-04-19

  The present invention encompasses compounds of general formula (1) wherein the groups R 1 to R 4 , X 1 , X 1 , X 3 , L 1 and L 2 are defined as in claim 1 , which are suitable for the treatment of diseases characterised by excessive or anomalous cell pro-liferation, and the use thereof in such a treatment.

  本发明涵盖了一般式（1）中的化合物，其中基团R1至R4、X1、X1、X3、L1和L2如权利要求1中定义的那样，适用于治疗以细胞过度或异常增殖为特征的疾病，并且在此类治疗中的使用。
• Azole derivatives and fused bicyclic azole derivatives as therapeutic agents
  申请人：Mjalli M. M. Adnan

  公开号：US20070213347A1

  公开（公告）日：2007-09-13

  This invention provides certain compounds, methods of their preparation, pharmaceutical compositions comprising the compounds, and their use in treating human or animal disorders. The compounds of the invention are useful as modulators of the interaction between the receptor for advanced glycated end products (RAGE) and its ligands, such as advanced glycated end products (AGEs), S100/calgranulin/EN-RAGE, β-amyloid and amphoterin, and for the management, treatment, control, or as an adjunct treatment for diseases in humans caused by RAGE. Such diseases or disease states include acute and chronic inflammation, the development of diabetic late complications such as increased vascular permeability, nephropathy, atherosclerosis, and retinopathy, the development of Alzheimer's disease, erectile dysfunction, and tumor invasion and metastasis.

  本发明提供了某些化合物、它们的制备方法、包含这些化合物的药物组合物，并且它们在治疗人类或动物疾病方面的用途。本发明的化合物可用作高级糖基化终产物受体（RAGE）和其配体（如高级糖基化终产物（AGEs）、S100/calgranulin/EN-RAGE、β-淀粉样蛋白和amphoterin）之间相互作用的调节剂，并用于管理、治疗、控制或作为辅助治疗RAGE引起的人类疾病。这些疾病或疾病状态包括急性和慢性炎症、糖尿病晚期并发症的发展，如增加的血管通透性、肾病、动脉粥样硬化和视网膜病变，阿尔茨海默病的发展、勃起功能障碍以及肿瘤浸润和转移。