2-amino-4-(carboxymethyl)-1,3-oxazole-5-carboxylic acid | 859721-42-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-amino-4-(carboxymethyl)-1,3-oxazole-5-carboxylic acid
• CAS: 859721-42-9
• 化学式: C₆H₆N₂O₅
• 分子量: 186.124
• InChiKey: DIDSKKRXQYKFEW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.42
• 重原子数：
  13.0
• 可旋转键数：
  3.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  126.65
• 氢给体数：
  3.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  2-amino-4-(carboxymethyl)-1,3-oxazole-5-carboxylic acid 在 sodium hydroxide 作用下， 反应 5.0h， 以60%的产率得到1-(5-oxo-2,5-dihydrofuran-3-yl)urea
  参考文献：
  名称：

  Synthesis and biological evaluation of sulfonamidooxazoles and β-keto sulfones: selective inhibitors of 11β-hydroxysteroid dehydrogenase type I

  摘要：

  The design, synthesis, and biological evaluation of arylsulfonamidooxazoles as 11 beta-HSD1 inhibitors and the serendipitous discovery of beta-keto sulfones as potent 11 beta-HSD1 inhibitors are described here. These two classes of compounds are not active against 11 beta-HSD2 and therefore may have significant therapeutic potential for metabolic syndrome, type 2 diabetes and related metabolic dysfunctions. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.03.093
• 作为产物：
  描述：

  dimethyl 2-bromo-3-oxoglutarate 在 sodium hydroxide 作用下， 以 乙醇 为溶剂， 反应 5.5h， 生成 2-amino-4-(carboxymethyl)-1,3-oxazole-5-carboxylic acid
  参考文献：
  名称：

  Synthesis and biological evaluation of sulfonamidooxazoles and β-keto sulfones: selective inhibitors of 11β-hydroxysteroid dehydrogenase type I

  摘要：

  The design, synthesis, and biological evaluation of arylsulfonamidooxazoles as 11 beta-HSD1 inhibitors and the serendipitous discovery of beta-keto sulfones as potent 11 beta-HSD1 inhibitors are described here. These two classes of compounds are not active against 11 beta-HSD2 and therefore may have significant therapeutic potential for metabolic syndrome, type 2 diabetes and related metabolic dysfunctions. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.03.093

文献信息

• Synthesis and biological evaluation of sulfonamidooxazoles and β-keto sulfones: selective inhibitors of 11β-hydroxysteroid dehydrogenase type I
  作者：Jason Xiang、Manus Ipek、Vipin Suri、Walt Massefski、Ning Pan、Ying Ge、May Tam、Yuzhe Xing、James F. Tobin、Xin Xu、Steve Tam

  DOI：10.1016/j.bmcl.2005.03.093

  日期：2005.6

  The design, synthesis, and biological evaluation of arylsulfonamidooxazoles as 11 beta-HSD1 inhibitors and the serendipitous discovery of beta-keto sulfones as potent 11 beta-HSD1 inhibitors are described here. These two classes of compounds are not active against 11 beta-HSD2 and therefore may have significant therapeutic potential for metabolic syndrome, type 2 diabetes and related metabolic dysfunctions. (c) 2005 Elsevier Ltd. All rights reserved.