871224-64-5

• 常用中文名：阿莫伦特
• 常用英文名：Almorexant
• CAS号：871224-64-5
• 分子式：C₂₉H₃₁F₃N₂O₃
• 分子量：512.563
• 相关类别： 信号通路 G 蛋白偶联受体/G 蛋白 食欲素受体(OX受体)
• 发布时间：2018-08-09 23:03:30
• 更新时间：2026-07-12 18:30:33
• Almorexant(ACT078573)是OX1和OX2受体拮抗剂,Ki分别为1.3和0.17 nM。

名称

• 中文名: 阿莫伦特
• 英文名: (R)-2-((R)-6,7-dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide
• 中文别名: 阿莫伦特杂质; (R)-2-((S)-6,7-二甲氧基-1-(4-(三氟甲基)苯乙基)-3,4-二氢异喹啉-2(1H)-基)-N-甲基-2-苯基乙酰胺; (R)-2-((S)-6,7-二甲氧基-1-(4-甲基苯乙基)-3,4-二氢异喹啉-2(1H)-基)-N-甲基-2-苯基乙酰胺; 阿莫伦特,10 MM DMSO 溶液
• 英文别名: ACT-078573;ACT 078573;ACT; 2-(6,7-dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide; (2R)-2-[(1S)-6,7-DIMETHOXY-1-[2-[4-(TRIFLUOROMETHYL)PHENYL]ETHYL]-3,4-DIHYDRO-1H-ISOQUINOLIN-2-YL]-N-METHYL-2-PHENYLACETAMIDE; (R)-2-{(S)-6,7-dimethoxy-1-[2-(4-trifluoromethylphenyl)ethyl]-3,4-dihydro-1H-isoquinolin-2-yl}-N-methyl-2-phenylacetamide; [3H]-Almorexant; 2(1H)-Isoquinolineacetamide, 3,4-dihydro-6,7-dimethoxy-N-methyl-α-phenyl-1-[2-[4-(trifluoromethyl)phenyl]ethyl]-, (αR,1S); 2(1H)-IsoquinolineacetaMide,3,4-dihydro-6,7-diMethoxy-N-Methyl-a-phenyl-1-[2-[4-(trifluoroMethyl)phenyl]ethyl]-1S); (2R)-2-((1S)-6,7-Dimethoxy-1-{2-(4-(trifluoromethyl)phenyl)ethyl}-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide; ((2R)-2-((1S)-6,7-dimethoxy-1-(2-(4-trifluoromethylphenyl)-ethyl)-3,4-dihydro-1H-isoquinolin-2-yl)-N-methyl-2-phenylacetamide); (2R)-2-[(1R)-6,7-Dimethoxy-1-{2-[4-(trifluoromethyl)phenyl]ethyl}-3,4-dihydro-2(1H)-isoquinolinyl]-N-methyl-2-phenylacetamide; (2R)-2-[(1S)-6,7-Dimethoxy-1-{2-[4-(trifluoromethyl)phenyl]ethyl}-3,4-dihydro-2(1H)-isoquinolinyl]-N-methyl-2-phenylacetamide; almorexant (ACT-078573); Almorexant [inn]; AlMorexant HCl; 3,4-Dihydro-6,7-dimethoxy-N-methyl-alpha-phenyl-1-[2-[4-(trifluoromethyl)phenyl]ethyl]-2(1H)-isoquinolineacetamide; (2R)-2-{(1S)-6,7-dimethoxy-1-[2-(4-trifluoromethyl-phenyl)-ethyl]-3,4-dihydro-1H-isoquinolin-2-yl}-N-methyl-2-phenyl-acetamide; pancreatic cancer,Orexin Rector (OX Rector),Pancreatic ductal adenoccinoma,Cataplexy,ACT078573,Almorexant,HCRT Rector,Inhibitor,Apoptosis,GPCR,orexin,Hypocretin Rector,Ca2+ channels,ncolsy,Caspase,HPAF-II cells,AsPC-1 cells,Calcium Channel,Ca channels,hypocretin,ACT-078573,inhibit,PDAC; Almorexant, 10 mM in DMSO; Act-078573 (R)-2-((R)-6,7-dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide; almorexant (ACT-078573), CID; Act-078573

物化性质

• 密度: 1.2±0.1 g/cm3
• 沸点: 620.4±55.0 °C at 760 mmHg
• 分子式: C₂₉H₃₁F₃N₂O₃
• 分子量: 512.563
• 闪点: 329.0±31.5 °C
• 精确质量: 512.228699
• PSA: 50.80000
• LogP: 5.89
• 蒸汽压: 0.0±1.8 mmHg at 25°C
• 折射率: 1.554
• 储存条件: -20°C，密闭，干燥

生物活性

• 描述: Almorexant(ACT078573)是OX1和OX2受体拮抗剂,Ki分别为1.3和0.17 nM。
• 相关类别:
  信号通路 >> G 蛋白偶联受体/G 蛋白 >> 食欲素受体(OX受体)
  研究领域 >> 神经疾病
• 参考文献:

  [1]. Cruz HG, et al. Assessment of the abuse liability of a dual orexin receptor antagonist: a crossover study of almorexant and zolpidem in recreational drug users. CNS Drugs. 2014 Apr;28(4):361-72.

  [2]. Malherbe P, et al. Biochemical and electrophysiological characterization of almorexant, a dual orexin 1 receptor (OX1)/orexin 2 receptor (OX2) antagonist: comparison with selective OX1 and OX2 antagonists. Mol Pharmacol. 2009 Sep;76(3):618-31.

  [3]. Sifferlen T, et al. Novel pyrazolo-tetrahydropyridines as potent orexin receptor antagonists. Bioorg Med Chem Lett. 2010 Mar 1;20(5):1539-42.

  [4]. Black SW, et al. Almorexant promotes sleep and exacerbates cataplexy in a murine model of narcolepsy. Sleep. 2013 Mar 1;36(3):325-36.

  [5]. Dayot S, et al. In vitro, in vivo and ex vivo demonstration of the antitumoral role of hypocretin-1/orexin-A and almorexant in pancreatic ductal adenocarcinoma. Oncotarget. 2018 Jan 9;9(6):6952-6967.

合成路线

769172-81-8 871224-68-9 ~% 871224-64-5

文献：WO2009/83899 A2, ; Page/Page column 28 ; WO2009/83903 A1, ; Page/Page column 28 ;

871224-77-0 593-51-1 ~% 871224-64-5

文献：WO2005/118548 A1, ; Page/Page column 28 ; WO 2005/118548 A1

769172-81-8 51685-62-2 ~% 871224-64-5

文献：WO2005/118548 A1, ; Page/Page column 29 ; WO 2005/118548 A1

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