体内
体外
药理学
EC50型
地塞米松
消炎药
化学
毒性
生物活性
医学
生物化学
生物
内科学
有机化学
生物技术
作者
Qingfu Lai,Tong Li,Fuli Zhang,Ming Li,Qinghua Mei,Lianbao Ye
标识
DOI:10.1002/slct.202104531
摘要
Abstract A series of imidazopyrazine derivatives were synthesized, and evaluated for their anti‐inflammatory activity in vitro and in vivo using RAW264.7 cells model and Zebrafish Traumatic Infection Inflammation model. The results in vitro showed that the compounds had significant inhibitory effect on inflammatory factor interleukin 6 (IL6), and N ‐ (3 ‐( 4‐ ((1,1‐dioxidothiomorpholino) methyl)phenyl) imidazo [1,5‐a] pyrazin‐6‐yl) cyclopropanecarboxamide A1 the best activity, which was significantly different from that of the lipopolysaccharide (LPS) control group ( P< 0.03). The experiment of anti‐inflammatory activity in vivo indicated that compound A1 showed obvious aggregation inhibitory activity on inflammatory effector cells which was significantly different from that in the tail‐cutting control group ( P< 0.03). When the concentration of the compound was 160 μ g/mL, the inhibitory activity of compound A1 was better than that of dexamethasone positive control group ( P< 0.05). This study could supply some anti‐inflammatory leading structure and possible mechanism for studying and developing new anti‐inflammatory agents.
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