(S)-4-benzyl-3-((S)-3-(4-hydroxyphenyl)-3-(isoxazol-3-yl)propanoyl)oxazolidin-2-one | 1011531-26-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: (S)-4-benzyl-3-((S)-3-(4-hydroxyphenyl)-3-(isoxazol-3-yl)propanoyl)oxazolidin-2-one
• 英文别名: (S)-4-benzyl-3-((S)-3-(4-(hydroxy)phenyl)-3-(isoxazol-3-yl)propanoyl)oxazolidin-2-one；(4S)-4-benzyl-3-[(3S)-3-(4-hydroxyphenyl)-3-(1,2-oxazol-3-yl)propanoyl]-1,3-oxazolidin-2-one
• CAS: 1011531-26-2
• 化学式: C₂₂H₂₀N₂O₅
• 分子量: 392.411
• InChiKey: ZJIWULVLEGAXMU-HKUYNNGSSA-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：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  92.9
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  (S)-4-benzyl-3-((S)-3-(4-hydroxyphenyl)-3-(isoxazol-3-yl)propanoyl)oxazolidin-2-one 在 lithium hydroxide monohydrate 、 双氧水 、 caesium carbonate 作用下， 以 四氢呋喃 、 二甲基亚砜 为溶剂， 反应 20.0h， 生成 (S)-3-(isoxazol-3-yl)-3-(4-((4-methyl-2-(4-(trifluoromethyl)phenyl)thiazol-5-yl)methoxy)phenyl)propanoic acid
  参考文献：
  名称：

  Optimization of GPR40 Agonists for Type 2 Diabetes

  摘要：

  GPR40 (FFA1 and FFAR1) has gained significant interest as a target for the treatment of type 2 diabetes. TAK-875 (1), a GPR40 agonist, lowered hemoglobin A1c (HbA1c) and lowered both postprandial and fasting blood glucose levels in type 2 diabetic patients in phase II clinical trials. We optimized phenylpropanoic acid derivatives as GPR40 agonists and identified AMG 837 (2) as a clinical candidate. Here we report our efforts in searching for structurally distinct back-ups for AMG 837. These efforts led to the identification of more polar GPR40 agonists, such as AM-4668 (10), that have improved potency, excellent pharmacokinetic properties across species, and minimum central nervous system (CNS) penetration.

  DOI：

  10.1021/ml400501x
• 作为产物：
  描述：

  (S)-3-乙酰基-4-苯甲基-2-唑烷酮 在 4-二甲氨基吡啶 、 二乙基异丙基胺 、 二碳酸二叔丁酯 、 三氯化硼-甲硫醚 、 四氯化钛 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 67.75h， 生成 (S)-4-benzyl-3-((S)-3-(4-hydroxyphenyl)-3-(isoxazol-3-yl)propanoyl)oxazolidin-2-one
  参考文献：
  名称：

  Optimization of GPR40 Agonists for Type 2 Diabetes

  摘要：

  GPR40 (FFA1 and FFAR1) has gained significant interest as a target for the treatment of type 2 diabetes. TAK-875 (1), a GPR40 agonist, lowered hemoglobin A1c (HbA1c) and lowered both postprandial and fasting blood glucose levels in type 2 diabetic patients in phase II clinical trials. We optimized phenylpropanoic acid derivatives as GPR40 agonists and identified AMG 837 (2) as a clinical candidate. Here we report our efforts in searching for structurally distinct back-ups for AMG 837. These efforts led to the identification of more polar GPR40 agonists, such as AM-4668 (10), that have improved potency, excellent pharmacokinetic properties across species, and minimum central nervous system (CNS) penetration.

  DOI：

  10.1021/ml400501x

文献信息

• Heterocyclic GPR40 Modulators
  申请人：Beck Hilary

  公开号：US20080090840A1

  公开（公告）日：2008-04-17

  The present invention provides compounds useful, for example, for treating metabolic disorders in a subject. Such compounds have the general formula I: where the definitions of the variables are provided herein. The present invention also provides compositions that include, and methods for using, the compounds in preparing medicaments and for treating metabolic disorders such as, for example, type II diabetes.

  本发明提供了一些化合物，例如用于治疗受试者的代谢紊乱。此类化合物具有一般式I，其中变量的定义在此提供。本发明还提供了包含这些化合物的组合物以及使用这些化合物制备药物和治疗代谢紊乱（例如II型糖尿病）的方法。
• Substituted biphenyl GPR40 modulators
  申请人：Brown Sean P.

  公开号：US20090111859A1

  公开（公告）日：2009-04-30

  The present invention provides compounds useful, for example, for treating metabolic disorders in a subject. Such compounds have the general formula I: where the definitions of the variables are provided herein. The present invention also provides compositions that include, and methods for using, the compounds in preparing medicaments and for treating metabolic disorders such as, for example, type II diabetes.

  本发明提供了一些有用的化合物，例如用于治疗受试者的代谢紊乱。这些化合物具有一般式I，其中变量的定义在此处提供。本发明还提供了包括这些化合物的组合物，以及使用这些化合物制备药物和治疗代谢紊乱的方法，例如II型糖尿病。
• HETEROCYCLIC GPR40 MODULATORS
  申请人：Beck Hilary

  公开号：US20100075974A1

  公开（公告）日：2010-03-25

  The present invention provides compounds useful, for example, for treating metabolic disorders in a subject. Such compounds have the general formula I: where the definitions of the variables are provided herein. The present invention also provides compositions that include, and methods for using, the compounds in preparing medicaments and for treating metabolic disorders such as, for example, type II diabetes.

  本发明提供了一些化合物，例如，用于治疗受试者的代谢紊乱。这些化合物具有一般式I：其中变量的定义在此提供。本发明还提供了包括这些化合物的组合物，以及使用这些化合物制备药物和治疗代谢紊乱的方法，例如类型II糖尿病。
• Heterocyclic GPR40 modulators
  申请人：Amgen Inc.

  公开号：US08003648B2

  公开（公告）日：2011-08-23

  The present invention provides compounds useful, for example, for treating metabolic disorders in a subject. Such compounds have the general formula I: where the definitions of the variables are provided herein. The present invention also provides compositions that include, and methods for using, the compounds in preparing medicaments and for treating metabolic disorders such as, for example, type II diabetes.

  本发明提供了一些化合物，例如用于治疗主体的代谢性疾病。这些化合物具有一般的公式I：其中变量的定义在此提供。本发明还提供包括上述化合物的组合物以及使用这些化合物制备药物和治疗代谢性疾病（例如2型糖尿病）的方法。
• WO2008/30520
  申请人：——

  公开号：——

  公开（公告）日：——