6-(1-piperazinyl)isoquinoline | 853687-09-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: 6-(1-piperazinyl)isoquinoline
• 英文别名: 6-piperazin-1-ylisoquinoline
• CAS: 853687-09-9
• 化学式: C₁₃H₁₅N₃
• 分子量: 213.282
• InChiKey: YRAWOBIYPTYSJG-UHFFFAOYSA-N

物化性质

• 沸点：
  417.7±25.0 °C(Predicted)
• 密度：
  1.152±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  16
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  28.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  6-(1-piperazinyl)isoquinoline 、 4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecane-9-sulfonyl chloride 在 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 为溶剂， 以17%的产率得到4-cyclopropyl-9-{[4-(6-isoquinolinyl)-1-piperazinyl] sulfonyl}-1-oxa-4,9-diazaspiro[5.5]undecan-3-one
  参考文献：
  名称：

  [EN] FATTY ACID SYNTHASE INHIBITORS
  [FR] INHIBITEURS DE L'ACIDE GRAS SYNTHASE

  摘要：

  公开号：

  WO2013177253A3
• 作为产物：
  描述：

  4-isoquinolin-6-yl-piperazine-1-carboxylic acid tert-butyl ester 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 生成 6-(1-piperazinyl)isoquinoline
  参考文献：
  名称：

  Discovery of imidazole carboxamides as potent and selective CCK1R agonists

  摘要：

  High-throughput screening revealed diaryl pyrazole 3 as a selective albeit modest cholecystokinin 1 receptor (CCK1R) agonist. SAR studies led to the discovery and optimization of a novel class of 1,2-diaryl imidazole carboxamides. Compound 44, which was pro. led extensively, showed good in vivo mouse gallbladder emptying (mGBE) and lean mouse overnight food intake (ONFI) reduction activities. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.06.057

文献信息

• Novel Inhibitors of Nicotinamide-N-Methyltransferase for the Treatment of Metabolic Disorders
  作者：Aimo Kannt、Sridharan Rajagopal、Mahanandeesha S. Hallur、Indu Swamy、Rajendra Kristam、Saravanakumar Dhakshinamoorthy、Joerg Czech、Gernot Zech、Herman Schreuder、Sven Ruf

  DOI：10.3390/molecules26040991

  日期：——

  Its expression in several cancer cell lines has been widely discussed in the literature, and recent work established a link between NNMT expression and metabolic diseases. Here we describe our approach to identify potent small molecule inhibitors of NNMT featuring different binding modes as elucidated by X-ray crystallographic studies.

  烟酰胺-N-甲基转移酶（NNMT）是催化从S-腺苷甲硫氨酸（SAM）到烟酰胺（Nam）的甲基转移的胞质酶。它在包括肝脏，脂肪组织和骨骼肌在内的许多组织中表达。其在几种癌细胞系中的表达已在文献中进行了广泛讨论，最近的工作建立了NNMT表达与代谢性疾病之间的联系。在这里，我们描述了我们的方法，以鉴定具有不同结合模式的NNMT的有效小分子抑制剂，如X射线晶体学研究所阐明的那样。
• AKT PROTEIN KINASE INHIBITORS
  申请人：Array Biopharma, Inc.

  公开号：EP1684694A2

  公开（公告）日：2006-08-02
• [EN] AKT PROTEIN KINASE INHIBITORS<br/>[FR] INHIBITEURS DE LA PROTEINE KINASE AKT
  申请人：ARRAY BIOPHARMA INC

  公开号：WO2005051304A2

  公开（公告）日：2005-06-09

  The present invention provides compounds, including resolved enantiomers, diastereomers, solvates and pharmaceutically acceptable salts thereof, comprising the Formula: A-L-CR where CR is a cyclical core group, L is a linking group and A is as defined herein. Also provided are methods of using the compounds of this invention as AKT protein kinase inhibitors and for the treatment of hyperproliferative diseases such as cancer.
• [EN] FATTY ACID SYNTHASE INHIBITORS<br/>[FR] INHIBITEURS DE L'ACIDE GRAS SYNTHASE
  申请人：GLAXOSMITHKLINE LLC

  公开号：WO2013177253A3

  公开（公告）日：2015-06-18
• Discovery of imidazole carboxamides as potent and selective CCK1R agonists
  作者：Cheng Zhu、Alexa R. Hansen、Thomas Bateman、Zhesheng Chen、Tom G. Holt、James A. Hubert、Bindhu V. Karanam、Susan J. Lee、Jie Pan、Su Qian、Vijay B.G. Reddy、Marc L. Reitman、Alison M. Strack、Vincent Tong、Drew T. Weingarth、Michael S. Wolff、Doug J. MacNeil、Ann E. Weber、Joseph L. Duffy、Scott D. Edmondson

  DOI：10.1016/j.bmcl.2008.06.057

  日期：2008.8

  High-throughput screening revealed diaryl pyrazole 3 as a selective albeit modest cholecystokinin 1 receptor (CCK1R) agonist. SAR studies led to the discovery and optimization of a novel class of 1,2-diaryl imidazole carboxamides. Compound 44, which was pro. led extensively, showed good in vivo mouse gallbladder emptying (mGBE) and lean mouse overnight food intake (ONFI) reduction activities. (c) 2008 Elsevier Ltd. All rights reserved.