(2RS,4R)-2-(1,3-diphenyl-1H-pyrazol-4-yl)thiazolidine-4-carboxamide | 1262005-12-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: (2RS,4R)-2-(1,3-diphenyl-1H-pyrazol-4-yl)thiazolidine-4-carboxamide
• 英文别名: (4R)-2-(1,3-diphenylpyrazol-4-yl)-1,3-thiazolidine-4-carboxamide
• CAS: 1262005-12-8
• 化学式: C₁₉H₁₈N₄OS
• 分子量: 350.444
• InChiKey: MQZMOJGPULPIFR-UCFFOFKASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  25
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.16
• 拓扑面积：
  98.2
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  tert-butyl (4R)-4-carbamoyl-2-(1,3-diphenylpyrazol-4-yl)-1,3-thiazolidine-3-carboxylate 在 盐酸 、 苯甲醚 作用下， 以 1,4-二氧六环 为溶剂， 以75%的产率得到(2RS,4R)-2-(1,3-diphenyl-1H-pyrazol-4-yl)thiazolidine-4-carboxamide
  参考文献：
  名称：

  Synthesis and biological evaluation of some thiazolylpyrazole derivatives as dual anti-inflammatory antimicrobial agents

  摘要：

  The synthesis of a novel series of 4-thiazolylpyrazolyl derivatives is described in the present report. All the newly synthesized compounds were examined for their anti-inflammatory activity using cotton pellet-induced granuloma and carrageenan-induced rat paw edema bioassays. Their inhibitory activities of cyclooxygenase-1 and cyclooxygenase-2 (COX-1 and COX-2), ulcerogenic effect and acute toxicity were also determined. Furthermore, all compounds were evaluated for their in vitro antimicrobial activity against Escherichia coli. Staphylococcus aureus and Candida albicans. A docking pose for compounds 8b, 10a and 10b separately in the active site of the human COX-2 enzyme and DNA-gyrase B was also obtained. The results revealed that compounds 8b, 10a and 10b exhibited good anti-inflammatory activity with no or minimal ulcerogenic effect and good safety margin. Compounds 10a and 10b were found to be the most potent anti-inflammatory agents in the present study. Meanwhile, 10a and 10b displayed higher selective inhibitory activity towards COX-2 compared to indomethacin. Moreover, compounds 10a and 10b exhibited promising antibacterial against both E. coli and S. aureus. Docking studies for 8b, 10a and 10b with COX-2 (PDB ID: 1CX2) and DNA-gyrase B (PDB ID: 1E11) showed good binding profile. (C) 2010 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2010.10.001