3-氨基奎宁环-3-羧酸 | 313643-39-9

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: 3-氨基奎宁环-3-羧酸
• 英文名称: 3-amino-1-azabicyclo[2.2.2]octane-3-carboxylic acid
• 英文别名: 3-aminoquinuclidine-3-carboxylic acid
• CAS: 313643-39-9
• 化学式: C₈H₁₄N₂O₂
• mdl: MFCD00126910
• 分子量: 170.211
• InChiKey: LXFNKALFOUSWOB-UHFFFAOYSA-N

物化性质

• 沸点：
  316.9±37.0 °C(Predicted)
• 密度：
  1.31±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -3
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.875
• 拓扑面积：
  66.6
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-氨基奎宁环-3-羧酸 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 反应 12.0h， 生成 (3-aminoquinuclidin-3-yl)methanol
  参考文献：
  名称：

  [EN] PROGRANULIN MODULATORS AND METHODS OF USING THE SAME
  [FR] MODULATEURS DE LA PROGRANULINE ET LEURS PROCÉDÉS D'UTILISATION

  摘要：

  本文提供了化合物的公式(I)，这些化合物可以调节前蛋白颗粒素，并且可以用于治疗与前蛋白颗粒素相关的疾病，如额颞叶痴呆症（FTLD）。

  公开号：

  WO2021081272A1
• 作为产物：
  描述：

  3-羟基喹洛啉-3-甲腈 在 盐酸 、 氨 作用下， 反应 96.0h， 生成 3-氨基奎宁环-3-羧酸
  参考文献：
  名称：

  (−)-Spiro[1-azabicyclo[2.2.2]octane-3,5‘-oxazolidin-2‘-one], a Conformationally Restricted Analogue of Acetylcholine, Is a Highly Selective Full Agonist at the α7 Nicotinic Acetylcholine Receptor

  摘要：

  Neuronal nicotinic acetylcholine receptors are members of the ligand-gated ion channel receptor superfamily and may play important roles in modulating neurotransmission, cognition, sensory gating, and anxiety. Because of its distribution and abundance in the CNS, the alpha7 nicotinic receptor is a strong candidate to be involved in some of these functions. In this paper we describe the synthesis and in vitro profile of AR-R17779, (-)-spiro[1-azabicyclo[2.2.2]octane-3,5'-oxazolidin-2'-one] (4a), a potent full agonist at the rat alpha7 nicotinic receptor, which is highly selective for the rat alpha7 nicotinic receptor over the alpha4 beta2 subtype. Preliminary SAR of AR-R17779 presented here indicate that there is little scope for modification of this rigid molecule as even minor changes result in significant loss of the alpha7 nicotinic receptor affinity.

  DOI：

  10.1021/jm000249r

文献信息

• QUINUCLIDINE, 1-AZABICYCLO[2.2.1]HEPTANE, 1-AZABICYCLO [3.2.1]OCTANE, and 1-AZABICYCLO[3.2.2]NONANE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS
  申请人：BRISTOL-MYERS SQUIBB COMPANY

  公开号：US20150322089A1

  公开（公告）日：2015-11-12

  The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.

  本披露提供了公式I的化合物及其盐，以及使用该化合物的组合物和方法。这些化合物是尼古丁α7受体的配体，可用于治疗中枢神经系统的各种疾病，特别是情感和神经退行性疾病。
• PROGRANULIN MODULATORS AND METHODS OF USING THE SAME
  申请人：ARKUDA THERAPEUTICS

  公开号：US20220409593A1

  公开（公告）日：2022-12-29

  Provided herein are compounds of formula (I) that modulate progranulin and methods of using the compounds in progranulin-associated disorders, such as Frontotemperal lobe dementia (FTLD).
• US9458179B2
  申请人：——

  公开号：US9458179B2

  公开（公告）日：2016-10-04
• [EN] PROGRANULIN MODULATORS AND METHODS OF USING THE SAME<br/>[FR] MODULATEURS DE LA PROGRANULINE ET LEURS PROCÉDÉS D'UTILISATION
  申请人：ARKUDA THERAPEUTICS

  公开号：WO2021081272A1

  公开（公告）日：2021-04-29

  Provided herein are compounds of formula (I) that modulate progranulin and methods of using the compounds in progranulin- associated disorders, such as Frontotemperal lobe dementia (FTLD).

  本文提供了化合物的公式(I)，这些化合物可以调节前蛋白颗粒素，并且可以用于治疗与前蛋白颗粒素相关的疾病，如额颞叶痴呆症（FTLD）。
• (−)-Spiro[1-azabicyclo[2.2.2]octane-3,5‘-oxazolidin-2‘-one], a Conformationally Restricted Analogue of Acetylcholine, Is a Highly Selective Full Agonist at the α7 Nicotinic Acetylcholine Receptor
  作者：George Mullen、James Napier、Michael Balestra、Thomas DeCory、Gregory Hale、John Macor、Robert Mack、James Loch、Ed Wu、Alexander Kover、Patrick Verhoest、Anthony Sampognaro、Eifion Phillips、Yanyi Zhu、Robert Murray、Ronald Griffith、James Blosser、David Gurley、Anthony Machulskis、John Zongrone、Alan Rosen、Jack Gordon

  DOI：10.1021/jm000249r

  日期：2000.11.1

  Neuronal nicotinic acetylcholine receptors are members of the ligand-gated ion channel receptor superfamily and may play important roles in modulating neurotransmission, cognition, sensory gating, and anxiety. Because of its distribution and abundance in the CNS, the alpha7 nicotinic receptor is a strong candidate to be involved in some of these functions. In this paper we describe the synthesis and in vitro profile of AR-R17779, (-)-spiro[1-azabicyclo[2.2.2]octane-3,5'-oxazolidin-2'-one] (4a), a potent full agonist at the rat alpha7 nicotinic receptor, which is highly selective for the rat alpha7 nicotinic receptor over the alpha4 beta2 subtype. Preliminary SAR of AR-R17779 presented here indicate that there is little scope for modification of this rigid molecule as even minor changes result in significant loss of the alpha7 nicotinic receptor affinity.