4-[(5-甲基-4-苯基-1,3-噻唑-2-基)氨基]-4-氧代丁酸 | 325471-38-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 中文名称: 4-[(5-甲基-4-苯基-1,3-噻唑-2-基)氨基]-4-氧代丁酸
• 英文名称: 4-((5-methyl-4-phenylthiazol-2-yl)amino)-4-oxobutanoic acid
• 英文别名: 4-[(5-Methyl-4-phenyl-1,3-thiazol-2-yl)amino]-4-oxobutanoic acid
• CAS: 325471-38-3
• 化学式: C₁₄H₁₄N₂O₃S
• 分子量: 290.343
• InChiKey: JTYCTMALSUYMEF-UHFFFAOYSA-N

物化性质

• 密度：
  1.354±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  108
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  methyl 4-[(5-methyl-4-phenyl-1,3-thiazol-2-yl)amino]-4-oxobutanoate 在 sodium hydroxide 、 盐酸 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 2.5h， 以66.5%的产率得到4-[(5-甲基-4-苯基-1,3-噻唑-2-基)氨基]-4-氧代丁酸
  参考文献：
  名称：

  Design, synthesis and biological evaluation of thiazole- and indole-based derivatives for the treatment of type II diabetes

  摘要：

  Present studies have shown that the lipid carrier has a significant role in several aspects of metabolic syndrome in A-FABP/ap2-deficient mice, including type 2 diabetes and atherosclerosis. 38 Thiazole- and indole-based derivatives were synthesized and investigated for their inhibitory effects on the production of LPS-stimulated TNF-alpha. Among them, 12b exhibited an excellent inhibitory efficiency compared to BMS309403 (95% vs. 85%) at the concentration of 10 mu M and a binding affinity for ap2 with the apparent K-i values 33 nM. Oral administration of 12b at a dosage of 50 mg/kg effectively reduced the levels of plasma blood glucose, triglycerides, insulin, total cholesterol and alanine aminotransferase in high-fat/diet-induced obesity model. The results highlighted that 12b was a potent anti-diabetic agent. (C) 2012 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2012.03.006