马悦颖, 尚明英, 李沧海, 霍海如, 蔡少青, 姜廷良. 桂枝汤有效成分苯丙烯类化合物干预IL-1β刺激小鼠脑微血管内皮细胞释放PGE2的构效关系J. 药学学报, 2007, 42(7): 798-802.
引用本文: 马悦颖, 尚明英, 李沧海, 霍海如, 蔡少青, 姜廷良. 桂枝汤有效成分苯丙烯类化合物干预IL-1β刺激小鼠脑微血管内皮细胞释放PGE2的构效关系J. 药学学报, 2007, 42(7): 798-802.
MA Yue-ying, SHANG Ming-ying, LI Cang-hai, HUO Hai-ru, CAI Shao-qing, JIANG Ting-liang. Structure-activity relationship of phenylallyl compounds inhibiting PGE2 release in mouse cerebral microvascular endothelial cells induced by IL-1βJ. Acta Pharmaceutica Sinica, 2007, 42(7): 798-802.
Citation: MA Yue-ying, SHANG Ming-ying, LI Cang-hai, HUO Hai-ru, CAI Shao-qing, JIANG Ting-liang. Structure-activity relationship of phenylallyl compounds inhibiting PGE2 release in mouse cerebral microvascular endothelial cells induced by IL-1βJ. Acta Pharmaceutica Sinica, 2007, 42(7): 798-802.

桂枝汤有效成分苯丙烯类化合物干预IL-1β刺激小鼠脑微血管内皮细胞释放PGE2的构效关系

Structure-activity relationship of phenylallyl compounds inhibiting PGE2 release in mouse cerebral microvascular endothelial cells induced by IL-1β

  • Abstract: To observe the effects of phenylallyl compounds on prostaglandin E2(PGE2)release in mouse cerebral microvascular endothelial cells (bEnd.3) stimulated by IL-1β, and to analyze their structure-activity relationship. Different concentrations of phenylallyl compounds were added separately, and the content of PGE2 induced by IL-1β in the culture media was measured by ELISA assay. The 50% inhibitory concentration (IC50) of PGE2 was calculated. Studies showed that phenylallyl compounds could affect the PGE2 release differently in bEnd.3 cells induced by IL-1β. Close relationships were shown between the inhibitory activities and the location and number of the substituent groups. In conclusion, phenylallyl compounds exhibited inhibitory activities at different extent on PGE2 release in bEnd.3 cells stimulated by IL-1β and presented certain structure-activity relationship.

     

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