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Synthesis and anti-inflammatory effects of a series of novel 9-O-substituted berberine derivatives

机译:一系列新型9-O取代的小檗碱衍生物的合成与抗炎作用

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摘要

Berberine owns multiple pharmacological activities, especially anti-inflammatory activity. To enhance the anti-inflammatory therapeutic efficiency of berberine, a series of novel 9-O-substituted berberine derivatives (5a-5d) were synthesized and their anti-inflammatory activities were evaluated. C-13-NMR, H-1-NMR, IR and high resolution mass spectrum (HRMS) results indicated that these derivatives were successfully synthesized. The xylene-induced inflammatory mice model demonstrated that these derivatives showed dose-dependent inhibition of ear inflammatory swelling. Comparing to berberine, ibuprofen and naproxen-modified berberine derivatives enhanced anti-inflammatory activities, while aspirin and nicotinic acid-modified berberine derivatives showed lower anti-inflammatory effects at the same dosages. This could be attributed to the enhanced inhibition of secretion of cytokines, including interleukin-6 and tumor necrosis factor-alpha, by ibuprofen and naproxen berberine derivatives, while aspirin and nicotinic acid berberine derivatives showed lower inhibition of tumor necrosis factor-alpha than berberine. These results suggest that ibuprofen and naproxen-modified berberine derivatives are promising new anti-inflammatory drug candidates.
机译:小檗碱拥有多种药理活动,特别是抗炎活动。为了增强小檗碱的抗炎治疗效率,合成了一系列新的9-O-取代的小檗碱衍生物(5A-5D),并评估其抗炎活性。 C-13-NMR,H-1-NMR,IR和高分辨率质谱(HRMS)结果表明这些衍生物被成功地合成。二甲苯诱导的炎性小鼠模型表明这些衍生物显示出剂量依赖性抑制耳炎症肿胀。与小檗碱,布洛芬和萘普生改性的小檗碱衍生物相比增强了抗炎活性,而阿司匹林和烟碱酸改性的小檗碱衍生物在相同剂量下表现出较低的抗炎作用。这可能归因于增强细胞因子分泌的抑制,包括白细胞介素-6和肿瘤坏死因子 - α,由布洛芬和萘普生小檗碱衍生物,而阿司匹林和烟碱酸的小檗碱衍生物表现出肿瘤坏死因子-α的抑制作用而不是小檗碱。这些结果表明,布洛芬和萘普生改性的小檗碱衍生物是具有新的抗炎药物候选者。

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