Ethyl 1-[(2-fluoro-5-methoxyphenyl)methyl]-6,7-dimethoxy-3,4-dihydroisoquinoline-4-carboxylate | 1344688-82-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异喹啉及其衍生物
• 英文名称: Ethyl 1-[(2-fluoro-5-methoxyphenyl)methyl]-6,7-dimethoxy-3,4-dihydroisoquinoline-4-carboxylate
• CAS: 1344688-82-9
• 化学式: C₂₂H₂₄FNO₅
• 分子量: 401.435
• InChiKey: QYOXBPVVKMSAQT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  29
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  66.4
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  Ethyl 1-[(2-fluoro-5-methoxyphenyl)methyl]-6,7-dimethoxy-3,4-dihydroisoquinoline-4-carboxylate 在 selenium(IV) oxide 、 lithium aluminium tetrahydride 、 sulfur 、 甲基磺酰氯 、 三乙胺 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 水 、 乙酸乙酯 为溶剂， 生成
  参考文献：
  名称：

  Discovery of 1-arylcarbonyl-6,7-dimethoxyisoquinoline derivatives as glutamine fructose-6-phosphate amidotransferase (GFAT) inhibitors

  摘要：

  Through high throughput screening and subsequent hit identification and optimization, we synthesized a series of 1-arylcarbonyl-6,7-dimethoxyisoquinoline derivatives as the first reported potent and reversible GFAT inhibitors. SAR studies of this class of compounds indicated significant impact on GFAT inhibition potency by substitutions on the A-ring and C-ring. The ketone group was found to be necessary for high potency. Compound 28 (RO0509347) demonstrated potent GFAT inhibition (IC(50) = 1 mu M) with a desirable pharmacokinetic profile in rats, and showed significant efficacy in reducing the glucose excursion in an OGTT test in ob/ob mice. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.09.009
• 作为产物：
  描述：

  2-氰基-2-(3,4-二甲氧基苯基)乙酸乙酯 在 盐酸 、 五氯化磷 、 palladium on activated charcoal 、 氢气 、 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 三乙胺 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 生成 Ethyl 1-[(2-fluoro-5-methoxyphenyl)methyl]-6,7-dimethoxy-3,4-dihydroisoquinoline-4-carboxylate
  参考文献：
  名称：

  Discovery of 1-arylcarbonyl-6,7-dimethoxyisoquinoline derivatives as glutamine fructose-6-phosphate amidotransferase (GFAT) inhibitors

  摘要：

  Through high throughput screening and subsequent hit identification and optimization, we synthesized a series of 1-arylcarbonyl-6,7-dimethoxyisoquinoline derivatives as the first reported potent and reversible GFAT inhibitors. SAR studies of this class of compounds indicated significant impact on GFAT inhibition potency by substitutions on the A-ring and C-ring. The ketone group was found to be necessary for high potency. Compound 28 (RO0509347) demonstrated potent GFAT inhibition (IC(50) = 1 mu M) with a desirable pharmacokinetic profile in rats, and showed significant efficacy in reducing the glucose excursion in an OGTT test in ob/ob mice. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.09.009

文献信息

• [EN] ISOQUINOLINE DERIVATIVES AND THEIR USE AS GFAT INHIBITORS<br/>[FR] INHIBITEURS DE LA GFAT
  申请人：HOFFMANN LA ROCHE

  公开号：WO2004101528A3

  公开（公告）日：2005-01-06