Novel 1-oxyl-2-substitutedphenyl-4, 4, 5, 5-tetramethylimidazolines: Synthesis, selectively analgesic action, and QSAR analysis
…, L Peng, YR Tang, C Wang, Z Zhang, S Peng
Index: Zhao, Ming; Li, Zheng; Peng, Li; Tang, Yu-Rong; Wang, Chao; Zhang, Ziding; Peng, Shiqi Bioorganic and Medicinal Chemistry, 2007 , vol. 15, # 8 p. 2815 - 2826
Full Text: HTML
Citation Number: 12
Abstract
Based on the knowledge that imidazoline can result in analgesic action due to its selective binding with the prostacyclin receptor, 20 1-oxyl-2-substitutedphenyl-4, 4, 5, 5- tetramethylimidazolines (3a–t) were prepared in moderate yields. At 0.13 mmol/kg dose, their in vivo analgesic activities were evaluated after the mice were administered at 30, 60, 90, and 150min. Compared with the pain threshold (12.27±9.56–17.71±7.00%) of normal ...
Related Articles:
[Gorini, Lapo; Caneschi, Andrea; Menichetti, Stefano Synlett, 2006 , # 6 p. 948 - 950]
[Tanimoto, Ryu; Suzuki, Shuichi; Kozaki, Masatoshi; Okada, Keiji Chemistry Letters, 2014 , vol. 43, # 5 p. 678 - 680]