Methyl 2-[2-[2-[4-(6-amino-6-oxohexyl)-3-oxo-1,4-benzoxazin-2-yl]ethoxy]phenyl]acetate | 374109-29-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并恶嗪类
• 英文名称: Methyl 2-[2-[2-[4-(6-amino-6-oxohexyl)-3-oxo-1,4-benzoxazin-2-yl]ethoxy]phenyl]acetate
• CAS: 374109-29-2
• 化学式: C₂₅H₃₀N₂O₆
• 分子量: 454.523
• InChiKey: YLUZGEGJGHLXLN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  33
• 可旋转键数：
  13
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  108
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  Methyl 2-[2-[2-[4-(6-amino-6-oxohexyl)-3-oxo-1,4-benzoxazin-2-yl]ethoxy]phenyl]acetate 在 sodium hydroxide 作用下， 以 甲醇 为溶剂， 生成 2-[2-[2-[4-(6-Amino-6-oxohexyl)-3-oxo-1,4-benzoxazin-2-yl]ethoxy]phenyl]acetic acid
  参考文献：
  名称：

  Benzoxazinones as PPARγ Agonists. 2. SAR of the Amide Substituent and In Vivo Results in a Type 2 Diabetes Model

  摘要：

  A series of benzoxazinones has been synthesized and tested for PPARgamma agonist activity. Synthetic approaches were developed to provide either racemic or chiral compounds. In vitro functional potency could be measured through induction of the aP2 gene, a target of PPARgamma. These studies revealed that compounds with large aliphatic chains at the nitrogen of the benzoxazinone were the most potent. Substitution of the chain was tolerated and in many cases enhanced the in vitro potency of the compound. Select compounds were further tested for metabolic stability, oral bioavailability in rats, and efficacy in db/db mice after 11 days of dosing. In vivo analysis with 13 and 57 demonstrated that the series has potential for the treatment of type 2 diabetes.

  DOI：

  10.1021/jm0301888
• 作为产物：
  描述：

  硝苯酚 在 palladium on activated charcoal 咪唑 、 三丁基膦 、 氢气 、 sodium hydride 、 potassium carbonate 、 N,N'-羰基二咪唑 、 1,1'-azodicarbonyl-dipiperidine 作用下， 以 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 苯 为溶剂， 20.0 ℃ 、344.74 kPa 条件下， 反应 40.0h， 生成 Methyl 2-[2-[2-[4-(6-amino-6-oxohexyl)-3-oxo-1,4-benzoxazin-2-yl]ethoxy]phenyl]acetate
  参考文献：
  名称：

  Benzoxazinones as PPARγ Agonists. 2. SAR of the Amide Substituent and In Vivo Results in a Type 2 Diabetes Model

  摘要：

  A series of benzoxazinones has been synthesized and tested for PPARgamma agonist activity. Synthetic approaches were developed to provide either racemic or chiral compounds. In vitro functional potency could be measured through induction of the aP2 gene, a target of PPARgamma. These studies revealed that compounds with large aliphatic chains at the nitrogen of the benzoxazinone were the most potent. Substitution of the chain was tolerated and in many cases enhanced the in vitro potency of the compound. Select compounds were further tested for metabolic stability, oral bioavailability in rats, and efficacy in db/db mice after 11 days of dosing. In vivo analysis with 13 and 57 demonstrated that the series has potential for the treatment of type 2 diabetes.

  DOI：

  10.1021/jm0301888

文献信息

• BIOLOGICALLY ACTIVE 4H-BENZO 1,4|OXAZIN-3-ONES
  申请人：Ortho-McNeil Pharmaceutical, Inc.

  公开号：EP1280784B1

  公开（公告）日：2007-06-27
• Benzoxazinones as PPARγ Agonists. 2. SAR of the Amide Substituent and In Vivo Results in a Type 2 Diabetes Model
  作者：Philip J. Rybczynski、Roxanne E. Zeck、Joseph Dudash、Donald W. Combs、Thomas P. Burris、Maria Yang、Melville C. Osborne、Xiaoli Chen、Keith T. Demarest

  DOI：10.1021/jm0301888

  日期：2004.1.1

  A series of benzoxazinones has been synthesized and tested for PPARgamma agonist activity. Synthetic approaches were developed to provide either racemic or chiral compounds. In vitro functional potency could be measured through induction of the aP2 gene, a target of PPARgamma. These studies revealed that compounds with large aliphatic chains at the nitrogen of the benzoxazinone were the most potent. Substitution of the chain was tolerated and in many cases enhanced the in vitro potency of the compound. Select compounds were further tested for metabolic stability, oral bioavailability in rats, and efficacy in db/db mice after 11 days of dosing. In vivo analysis with 13 and 57 demonstrated that the series has potential for the treatment of type 2 diabetes.